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Circadian Clocks and Inflammation: Reciprocal Regulation and Shared Mediators

  • Nicolas Cermakian
  • Susan Westfall
  • Silke Kiessling
Review

Abstract

The immune system is deeply interconnected with the endogenous 24-h oscillators of the circadian system. Indeed, the connection between these two physiological systems occurs at multiple levels and in both directions. On one hand, various aspects of the immune system show daily rhythms, which appear to be essential for healthy immune maintenance and proper immune response. On the other hand, immune responses cause changes in circadian rhythms, disrupting their delicate balance and manifesting in disease. Indeed, immune challenges cause various time-, gene-, and tissue-specific effects on circadian-regulated factors. This article reviews the possible mediators of the cross talk between the circadian clock and the immune system, in particular the inflammatory pathways. The rhythmic expression of cytokines and their receptors, as well as other rhythmically regulated humoral factors such as glucocorticoids, melatonin, leptin, or prostaglandins, could gate the effects of the immune response on the circadian system. In addition, systemic cues such as body temperature and neuronal connections between the brain and peripheral tissues may underlie the immune–circadian communication.

Keywords

Circadian rhythm Clock gene Cytokine Fever Innate immunity Inflammation 

Abbreviations

AA-NAT

Arylalkylamine-N-acetyltransferase

BMAL1

Brain and muscle ARNT-like protein 1

CLOCK

Circadian locomotor output cycles kaput

CRY

Cryptochrome

DBP

D-box binding protein

GC

Glucocorticoid

HPA

Hypothalamic–pituitary–adrenal

HSP

Heat-shock proteins

HSF

Heat-shock factor

IFN

Interferon

IL

Interleukin

LPS

Lipopolysaccharide

NFκB

Nuclear factor of kappa light polypeptide gene enhancer in B cells

NK cell

Natural killer cell

PER

Period

PGE2

Prostaglandin E2

PNS

Parasympathetic nervous system

RA

Rheumatoid arthritis

ROR

Retinoic acid receptor-related orphan receptor

SCN

Suprachiasmatic nucleus

SNS

Sympathetic nervous system

TNF-α

Tumor necrosis factor α

Circadian Clocks

Circadian rhythms organize physiological systems in time and align them to the 24-h environmental cycles (an explanation of chronobiology-related terms can be found in Table 1). Environmental cues including the light–dark, feeding, and temperature cycles adjust the timing of these endogenous rhythms. The circadian system confers adaptability and predictability in biology, ultimately maintaining homeostasis in health and well-being (Hastings et al. 2007; Nakagawa and Okumura 2010).
Table 1

Definition of chronobiology concepts used in the text

Term

Definition

Example

Circadian rhythm

Rhythm with a period of about 24 h, which persist in the absence of external timing cues. To observe circadian rhythms, one must use experimental conditions without time cues. If an experiment is done under conditions that provide timing cues (e.g., a light/dark cycle), one cannot distinguish between the effects of the external/environmental timing signal or the endogenous circadian system, and hence, one should talk of a daily rhythm rather than an internal circadian rhythm

Melatonin secretion and core body temperature both present circadian rhythms in animals, as these rhythms persist in constant conditions, with a period close to 24 h

Entrainment

Alignment of an endogenous rhythm to an external timing cue

Even though the endogenous period of the internal clocks is slightly different from 24 h, the environmental light/dark cycle can entrain them to a 24-h-long day

Free-running period

Period (duration of a full cycle) of the endogenous circadian clock. The free-running period can be observed in the absence of environmental timing cues, i.e., under constant laboratory conditions

The free-running period of human subjects is on average slightly above 24 h

Subjective day/night

Under constant laboratory conditions, subjective day and night correspond to the parts of the cycles equivalent to day and night, respectively

The laboratory mouse is a nocturnal animal, active in the night under a light/dark cycle; thus, under constant darkness conditions, the part of the cycle when the mouse is active will be called the subjective night

SCN

The site of the central circadian clock in mammals located in the anterior hypothalamus

The SCN aligns to the environmental light/dark cycle and in turn controls physiological rhythms, e.g., the rhythmic release of hormones into the blood stream

Phase-shift

Change in the timing of a rhythm, generally following an external timing cue. When the resulting phase is later than the original phase, one will talk of a phase delay; when the resulting phase is earlier than the original phase, one will talk of a phase advance

A light stimulation in the early night (e.g., 8 p.m) moves the onset of the locomotor activity of a mouse from 6 to 7 p.m. (phase delay)

Circadian rhythms are generated by clocks present in most tissues and cell types (Dibner et al. 2010). At the molecular level, these circadian clocks are composed of a number of clock genes including circadian locomotor output cycles kaput (Clock); brain and muscle ARNT-like protein 1 (Bmal1); cryptochrome (Cry)1 and 2; and period (Per)1, 2, and 3, which are involved in an autoregulatory transcriptional–translational feedback loop (Duguay and Cermakian 2009). Additional feedback loops add further levels of complexity, robustness, and a means of regulation to the basic feedback loop. These accessory feedback loops involve other transcription factors such as the orphan nuclear receptors REV-ERB α and β and retinoic acid receptor-related orphan receptor (ROR) α, β, and γ (Duguay and Cermakian 2009). The central pacemaker resides in the suprachiasmatic nucleus (SCN) of the anterior hypothalamus and coordinates rhythms in peripheral clocks through a variety of neuronal, humoral, and behavioral cues (Fig. 1) (Dibner et al. 2010). Peripheral clocks are autonomous but without the SCN, rhythms in individual cells or tissues eventually desynchronize (Nagoshi et al. 2004; Yamazaki et al. 2000; Yoo et al. 2004). Although many cues have been proposed to contribute to the communication between central and peripheral clocks, each tissue seems to respond to a unique set of cues, which are yet to be elucidated in most cases (Dibner et al. 2010).
Fig. 1

Organization of the circadian system and mediators affected by inflammation. In mammals, the central circadian clock is located in the suprachiasmatic nuclei (SCN) of the hypothalamus. The SCN clock can be entrained by day–night cycles via input from the retina. Many other brain regions and most peripheral tissues have intrinsic circadian clocks. Although these peripheral clocks can drive circadian rhythms on their own, within the organism, their rhythms are coordinated by the SCN central clock. This can occur via different types of rhythmic cues, which can all be controlled by the central clock: humoral cues (such as hormones or cytokines), neural pathways (via the autonomic nervous system: ANS), and systemic cues (such as temperature and feeding rhythms). Gray lightning symbols indicate clocks and mediators known to be affected in conditions of immune challenge or inflammation. This scheme is over-simplified in that mediators can also act for the communication between peripheral clocks, or from peripheral clocks back to the central clock or its resetting by light signals. PGE 2 prostaglandin E2, SNS sympathetic nervous system, PNS parasympathetic nervous system, CBT core body temperature

Many of the cues involved in the communication between circadian clocks are common with immune pathways (e.g., glucocorticoids (GCs) and cytokines). This suggests that immune responses may interfere with circadian clock regulation. Indeed, following an immune challenge, there are notable perturbations in circadian homeostasis. At the same time, rhythmicity in immune mediators is prone to impact on immune responses. Exactly how immune responses and clock mechanisms influence each other is a keen topic of investigation, and the progress toward elucidating these mechanisms will be discussed, with focus on mammals.

Circadian Rhythms in the Immune System

Many immune cell types show daily variations in cell counts in the blood of humans and rodents (Abo et al. 1981; Born et al. 1997; Haus and Smolensky 1999; Lange et al. 2010). This includes T and B lymphocytes, monocytes, macrophages, natural killer (NK) cells, neutrophils, and eosinophils. In addition, the production of various cytokines including interleukin (IL)-6, IL-1β, interferon (IFN)-γ, and tumor necrosis factor (TNF)-α is rhythmic in macrophages, T cells, adipose tissue, and spleen (Ando et al. 2011; Bollinger et al. 2011; Keller et al. 2009).

Many of the studies investigating these rhythms were performed under regular light–dark and sleep–wake conditions, making it impossible to tell whether the rhythms are due to the endogenous circadian system or to the cyclic environmental cues. In some studies (Ackermann et al. 2012; Benedict et al. 2007; Born et al. 1997), samples collected from human subjects during a sleep–wake cycle and during a day of sleep deprivation were compared. The data showed that immune variables were differentially regulated by the sleep–wake cycle: some rhythms were very similar in both experimental conditions, indicating little regulation by sleep or wake, and involvement of the circadian system; others were in good part or totally dependent on the sleep–wake cycle. The reader is referred to the literature cited above for more details.

Rhythmic hormones such as cortisol and noradrenaline seem to have a role to play in shaping the rhythm of abundance of immune cell populations. In mice, the daily variations of lymphocyte counts are lost following adrenalectomy (Kawate et al. 1981). In humans, blood counts of CD4+ and CD8+ naive, central memory, and effector memory T lymphocytes drop after cortisol injection (Dimitrov et al. 2009), and conversely, the opposite effect is observed when cortisol levels are pharmacologically reduced or an antagonist of the GC receptor is used (Besedovsky et al. 2014). These data suggest that the decreased numbers of these cells in the morning is due to the high morning cortisol levels. These effects of cortisol on T-cell population rhythms are inversely correlated with the expression of chemokine receptor CXCR4 in these cells, mediating T-cell redistribution (bone marrow homing) in response to cortisol (Besedovsky et al. 2014; Dimitrov et al. 2009). In contrast to the T-cell subsets described above, CD8+ effector T-cell count rise upon noradrenaline injection, which links the normal rise of this subclass of cells in the morning to the high morning noradrenaline levels (Dimitrov et al. 2009). Noradrenaline appears to stimulate demargination from the vascular endothelium via high chemokine receptor CX3CR1 expression in these cells (Dimitrov et al. 2009). Accordingly, studies in mice showed a daily rhythm of leukocyte recruitment to bone marrow and skeletal muscle (Scheiermann et al. 2012). This rhythm is controlled by the central clock, via the sympathetic nervous system (SNS), which induces a daily oscillation of adhesion molecules and chemokines. In contrast, in rats subjected to constant light conditions (conditions abolishing the rhythms of locomotor activity and catecholamines), the 24-h variations of lymphocyte counts were still observed (Depres-Brummer et al. 1997). The apparent discrepancy could be due to species differences or to the different conditions and measures among the experiments.

The rhythms described above for the levels of immunocompetent cells and cytokines suggest that immune functions may also present a variation across the day and possibly be under the endogenous control of the circadian system itself. Indeed, evidence for the rhythmic regulation of immune functions has begun to be uncovered with the use of mice with mutations in clock genes. For example, mice mutant for the gene Clock lose rhythmicity in many immunoregulatory genes (Oishi et al. 1998). Bmal1-deficient mice, which lack a functional clock, have lower B-cell counts compared to wild-type (WT) mice, but normal levels of B-cell precursors in the bone marrow, suggesting a defect in B-cell development (Sun et al. 2006).

Recent reports have shown that the function of T lymphocytes is controlled by the circadian system (Bollinger et al. 2011; Esquifino et al. 2004; Fortier et al. 2011; Kirsch et al. 2012). In vitro stimulation with PMA/ionomycin of CD4+ T cells harvested at different times of day showed daily variation in cytokine production (Bollinger et al. 2011) and proliferation (Fortier et al. 2011). While PMA/ionomycin activate cell proliferation by acting on intracellular signalling pathways (intracellular calcium, protein kinase C), other experiments have looked more upstream in T-cell activation pathways, i.e., at the level of the T-cell receptor and antigen presentation to the T cells. When T cells were stimulated through their T-cell receptor using the mitogen concanavalin A (Esquifino et al. 2004) or anti-CD3 T-cell receptor chain antibody (Fortier et al. 2011), rhythms of proliferation were also found. Moreover, immunization of mice using dendritic cells carrying an antigen led to a much stronger antigen-specific activation when injections were administered in the day than in the night (Fortier et al. 2011). Finally, recent data have indicated that the circadian clock in T lymphocyte is key to the development of the TH17 subtype (Yu et al. 2013). Altogether, these reports show that the response of T lymphocytes to antigen presentation, the subsequent cell expansion and acquisition of effector function, and the differentiation into different T-cell subtypes are all under daily regulation.

While these studies on rhythm in the response to antigen presentation are crucial and may lead to better control of infectious disease as well as more efficient vaccination schemes, the focus of the remainder of the present review will be on the innate immune system, the inflammatory response, and their cross talk with the circadian system. Likewise, over the past decade, many reports have shown an intricate relationship between the circadian system and cells of the innate immune system such as NK cells and macrophages.

The secretion of cytokines (IFN-γ, TNF-α) and cytolytic factors (granzyme B, perforin) by NK cells follows a rhythm in rat and mouse spleens (Arjona and Sarkar 2005; Logan and Sarkar 2012). NK cells express clock genes, and the knockdown of their expression dampens the rhythm of cytolytic factors (Arjona and Sarkar 2008). Similarly, subjecting rats to a repeated jet lag protocol disrupts both clock gene expression and rhythms of cytokine and cytolytic factor secretion by NK cells and reduces their cytotoxicity (Logan and Sarkar 2012). Since the same experimental protocol promoted tumor growth, and given the role of NK cells in tumor surveillance, the authors suggested that disruption of the clock in NK cells may promote tumor development (Logan et al. 2012).

Many articles have delineated a role for the clock in regulating monocyte and macrophage functions. Phagocytic activity of macrophages was shown to vary over the day–night cycle in mice (Hayashi et al. 2007). Also, secretion of cytokines following lipopolysaccharide (LPS) treatment of macrophages in vitro or LPS injection in mice follows a circadian rhythm, with higher secretion of TNF-α, IL-6, and other cytokines in the early subjective night than in the early subjective day (Gibbs et al. 2012; Keller et al. 2009). Notably, this diurnal secretion was shown to be dependent on a functional circadian clock in macrophages (Gibbs et al. 2012). A rhythm in abundance of the REV-ERBα transcription factor, itself controlled by the circadian clock in macrophages, was demonstrated to regulate in a circadian fashion a broad array of genes important for cytokine synthesis and secretion (Gibbs et al. 2012; Keller et al. 2009; Sato et al. 2014). Interestingly, subjecting mice to a chronic jet lag protocol increases the cytokine response to LPS in vivo and in cultured peritoneal macrophages (Castanon-Cervantes et al. 2010).

Recent studies have highlighted the importance of the clock in monocytes and macrophages for the response to pathogens. Bmal1 gene expression in Lys6Chi inflammatory monocytes was found to be important for their oscillation in numbers, to modulate the recruitment of these cells to the site of Listeria monocytogenes infection, and to control the pathogenicity of these bacteria (Nguyen et al. 2013). Similarly, a time dependence of cytokine response of macrophages to Salmonella typhimurium infection was found (Bellet et al. 2013). Moreover, reduced cytokine secretion from macrophages of Clock gene mutant mice was observed after LPS treatment of the cells in vitro or after S. typhimurium infection of the mice (Bellet et al. 2013).

Daytime Dependence of the Response to Endotoxin Administration

LPS is a molecule of the Gram-negative bacteria’s coat that can bind Toll-like receptor 4 (TLR4) on the surface of different cell types (Lu et al. 2008). Binding of LPS to TLR4 leads to the oligomerization of this receptor, the activation of different signalling pathways, and then the upregulation of a large battery of pro-inflammatory cytokines and chemokines (such as IL-1, IL-6, TNF-α, and CCL2) (Rossol et al. 2011). This action of LPS ultimately provokes a strong febrile and systemic inflammatory response (Raetz and Whitfield 2002).

Interestingly, the risk of lethality induced by LPS depends on the time of administration (Halberg et al. 1960; Marpegan et al. 2009). Rodents treated with LPS late in the rest phase have a much higher risk of mortality than those treated during the active phase, which is correlated to the magnitude of pro-inflammatory cytokines induction (Halberg et al. 1960; Kitoh et al. 2005; Marpegan et al. 2009). In mice, time-of-day dependence was observed for lethality following TNF-α injections (Hrushesky et al. 1994) and upon cecal ligation and puncture, an experimental model of sepsis (Silver et al. 2012). A modulation of inflammatory responses across the day also takes place in humans (Petrovsky et al. 1998; Pollmacher et al. 1996). For example, people suffering from sepsis are more likely to die in the early morning (Hrushesky et al. 1994; Sam et al. 2004).

The daily pattern of LPS-induced mortality in rodents is not observed under constant darkness conditions (Marpegan et al. 2009), perhaps due to a loss of the rhythmic upregulation of pro-inflammatory cytokines. One report in humans showed that TNF-α and IL-12 were not rhythmic in subjects kept in constant conditions including sleep deprivation, whereas IL-6 was the only cytokine that maintained its rhythmicity (Lange et al. 2010). These studies suggest the rhythmic responses to LPS are driven by environmental factors. Consistent with an impact of environmental light cues, animals housed in constant light (Carlson and Chiu 2008) or on repeated jet lag conditions (Castanon-Cervantes et al. 2010) are more prone to LPS-induced mortality than animals housed in a regular light–dark cycle. However, in sharp contrast to the studies mentioned above that seem to exclude a direct implication of the circadian clock, Per2 mutant mice are resistant to endotoxic shock and produce lower levels of pro-inflammatory cytokines (Liu et al. 2006). Further, the time-dependent risk of mortality induced by endotoxin is lost in these mutants. This implies a role for the circadian clock in the severity of an endotoxic shock in mice.

Effects of Endotoxin Administration on Circadian Rhythmicity

As reported in the previous section, there is a clear daily regulation of the inflammatory response to endotoxin administration. Recent research has shown that the converse is also true: circadian rhythms are altered in experimental models of inflammation. For example, clock-regulated behaviors such as sleep–wake cycle, movement, and food intake are all altered by systemic inflammation (Dantzer 2001). In addition, LPS, IL-1, or TNF-α can all phase-shift activity rhythms, but only when animals are treated early in the active phase (Leone et al. 2012; Marpegan et al. 2005).

Studies have shown that inflammation can impact on SCN function. At the molecular level, LPS treatment suppresses the expression of Per2 and D-box binding protein (Dbp) in the SCN (Okada et al. 2008). Acute LPS administration induces Fos protein expression in the SCN. While light induces Fos throughout the whole SCN and in particular in the ventro-lateral part of the nucleus, LPS induces Fos only in the dorso-medial part of the SCN, which is reminiscent of the effect of other non-photic treatments (Marpegan et al. 2005). Of note, the effects of inflammation on the circadian system are not only acute. Indeed, LPS challenge in mice can induce long-term (3–4 months) changes on light-induced behavioral phase-shifts and PER2 protein expression in the SCN (O’Callaghan et al. 2012). In another study, LPS was administered chronically (for 2 months), which led to an attenuation of the response of the SCN to light signals (Palomba and Bentivoglio 2008). Notably, all the studies looking at central effects of inflammation have used peripheral LPS treatment. Understanding how the signals reach the SCN will require additional research.

Inflammation also affects clock gene expression in the periphery. LPS administration suppresses the expression of Per1 and Per2 in the liver (Okada et al. 2008). LPS-dependent suppression of clock genes in the liver depends on the time of injection (Yamamura et al. 2010). Similarly, in another model of inflammation, the intramuscular injection of turpentine oil in rats, tissue-specific and time-dependent effects on clock gene expression were observed (Westfall et al. 2013). In human subjects, LPS injection suppresses clock gene mRNA levels (Haimovich et al. 2010), while in horses, LPS injection was shown to induce the expression of Per2 and Bmal1 (Murphy et al. 2007).

In summary, studies have shown a diurnal regulation of the inflammatory response on one hand and strong effects of inflammation on circadian clocks on the other hand. We propose that immune responses and circadian mechanisms overlap. In particular, the inflammatory response impinges onto pathways and mediators important for the regulation of peripheral clocks (Fig. 1), while circadian clocks and their rhythmic outputs modulate the immune response (Fig. 2). The next sections will describe possible mediators for the cross talk between the innate immune system and circadian clocks. In each case, we will go over the circadian regulation of the mediators and then over their feedback on circadian rhythms.
Fig. 2

Circadian rhythms in the immune system. An immune challenge (e.g., infection or treatment with bacterial wall endotoxin lipopolysaccharide: LPS) involves the function of various cell types of the innate immune system (e.g., NK cells, monocytes, macrophages, and dendritic cells) and the adaptive immune system (B and T lymphocytes; only the latter shown here). Components of the molecular circadian clock were found in many of these cell types (symbolized by gray clock symbols). Accordingly, studies have illustrated circadian rhythms in the function of these immunocompetent cells (symbolized by gray rhythm curve symbols), in particular rhythms in the secretion by these cells of cytokines, chemokines, and cytolytic factors, in the ability to migrate to the site of infection and kill pathogens, and in the effectiveness of the response to antigen presentation and acquisition of effector function by T cells

Cytokines as Mediators of the Immune–Circadian Interaction

Cytokines are the main communication factors of the immune system. Many pro-inflammatory cytokines show a diurnal variation, with peak levels generally observed during the rest phase both in nocturnal rodents (light phase) (Haus and Smolensky 1999) and humans (dark phase) (Guan et al. 2005; Pollmacher et al. 1996). Expression of cytokine receptors can also oscillate. For example, the IFN-γ and IL-1 receptors are rhythmically expressed in the rodent SCN (Beynon and Coogan 2010; Lundkvist et al. 1998; Sadki et al. 2007). Moreover, as mentioned before, the magnitude of the cytokine response to LPS treatment varies over time. Here, for different cytokines, we will go over their daily regulation as well as their known effects on the circadian system.

Tumor Necrosis Factor α

There is a clear bidirectional regulation between Cry clock genes and TNF-α. CRY1 can directly reduce the transactivation of the TNF-α gene (Hashiramoto et al. 2010). Accordingly, in Cry1/Cry2 knockout (KO) mice, TNF-α levels are higher and the arthritic score is worsened in an induced arthritic experimental model (Hashiramoto et al. 2010). In addition, Cry KO mice are sensitized to TNF-α-induced apoptosis through the inhibition of nuclear factor of kappa light polypeptide gene enhancer in B-cell (NFκB) signalling (Lee and Sancar 2011).

Treatment of fibroblasts with TNF-α was shown to inhibit the CLOCK/BMAL1-mediated transactivation of clock genes with E-boxes (Cavadini et al. 2007; Petrzilka et al. 2009). Actually, subcutaneous infusion of TNF-α downregulates a battery of clock genes in the mouse liver (Cavadini et al. 2007). As TNF-α is rhythmically released from NK cells under constant conditions (Arjona and Sarkar 2006), TNF-α might be implicated in the time-dependent regulation of clock gene expression. A modulation of clock gene expression by TNF-α is also observed in human primary rheumatoid synovial cells, but in this case, the effect was proposed to be mediated by PAR bZip transcription factors such as DBP and E4BP4 (Yoshida et al. 2013). This observation in cultured rheumatoid synovial cells may explain the altered clock gene expression in a mouse model of arthritis (Hashiramoto et al. 2010).

TNF-α can also act on the SCN. When injected intracerebroventrically in mice, TNF-α causes a phase delay in locomotor activity rhythms (Leone et al. 2012), while a cocktail composed of TNF-α and IFN-γ activates the expression of the Fos protein in the SCN, differentially according to time of day (Sadki et al. 2007). In vitro, TNF-α addition to slice preparations leads to an increase in spontaneous firing rate of SCN neurons (Nygard et al. 2009). Moreover, TNF-α phase-shifts PER2 expression rhythms in cultured SCN astrocytes (Duhart et al. 2013). Furthermore, an involvement of TNF-α in the response of the SCN to LPS was suggested: blocking TNF action using a soluble form of its receptor attenuates the response to LPS in the SCN (Leone et al. 2012). Importantly, the TNF-α receptor is expressed in the mouse SCN, with a daily rhythm (Sadki et al. 2007), suggesting a physiological role for this cytokine in regulating the central clock.

Interferon

Depending on the time of IFN-α treatment in mice, different effects are noted on the SCN central clock. Subcutaneous injection at the beginning of the active phase, but not at the beginning of the rest phase, blunts Per and Bmal1 rhythms in the SCN (Ohdo et al. 2001). These changes are accompanied by suppressed locomotor activity and body temperature rhythms. Similarly, continuous administration of IFN-α to mice using a mini-pump reduces CLOCK and BMAL1 protein levels in the SCN and dampens the expression of genes controlled by these transcription factors (e.g., Per genes, Cry1, vasopressin) (Koyanagi and Ohdo 2002). This treatment also reduces the amplitude of the locomotor activity rhythms. As for IFN-γ, its application on SCN slices decreases the spontaneous excitatory postsynaptic activity and chronic treatment blunts Per1 expression rhythms in SCN culture (Kwak et al. 2008). In addition, IFN-γ phase advances the clock in hamsters upon intracerebroventricular injection in the middle of the day, but not when injected in the middle of the night (Boggio et al. 2003).

IFNs also modify clock gene expression in the periphery. The downregulation of Clock and Bmal1 genes by IFN-α in hepatocytes was attributed to a signal transducer and activator of transcription 1-dependent mechanism (Koyanagi and Ohdo 2002). IFN-α was also found to downregulate Per1 and Dbp genes in the liver (Koyanagi and Ohdo 2002). Interestingly, the rhythmic expression of IFN-α/β receptors in the mouse liver gates the antiviral effect of IFN-α (Koyanagi et al. 2006). Of note though, acute treatment of fibroblasts in culture with either IFN-α or IFN-γ has no effect on the levels of Per mRNAs (Cavadini et al. 2007).

IL-6

Evidence is scarcer for a role of IL-6 as a circadian–immune mediator. As mentioned above, IL-6 secretion by macrophages in response to an endotoxin challenge varies with the time of treatment. A similar time dependence was observed when treating whole blood with LPS, and as with macrophages, environmental circadian disruption also increased the IL-6 response in this model (Adams et al. 2013). On the other hand, IL-6 itself might affect on circadian clocks. Indeed, IL-6 was shown to induce the expression of the Per1 promoter in cultured cells (Motzkus et al. 2002). Following an inflammatory challenge, the suppression of clock gene expression in the liver and heart parallels the induction of IL-6. For example, following turpentine oil injection, maximal IL-6 induction and Per mRNA suppression both occur after 8–10 h (Westfall et al. 2013). In this system, IL-6 is the only pro-inflammatory cytokine outside of the site of localized inflammation, suggesting that it may have a role in the effects of turpentine injection on clock genes. However, data argue against a direct causative role of IL-6 in clock gene regulation at least in the liver: it was shown that turpentine-induced suppression of clock genes occurs despite inhibition of IL-6 induction by the IL-1 receptor antagonist and further, in culture, IL-6 has no effect on clock genes in liver-derived cells (Westfall et al. 2013) or in fibroblasts (Cavadini et al. 2007).

Nuclear Factor of κ Light Polypeptide Gene Enhancer in B Cells

NFκB is one of the major transcription factors activated downstream of cytokine and LPS receptors and it is critical for the mounting of an immune response (Vallabhapurapu and Karin 2009). Several recent studies have highlighted various connections between NFκB and molecular clock mechanisms: (1) CLOCK protein binds to NFκB and regulates its transcriptional activity (Spengler et al. 2012). Accordingly, NFκB activation is reduced in Clock KO mice (Spengler et al. 2012). (2) In Cry1/Cry2 double KO cells (which are clock-deficient), NFκB activation following TNF-α treatment was weaker than in WT cells (Lee and Sancar 2011). In this case, instead of a direct action of CLOCK on NFκB, the circadian control of NFκB activity is mediated by a circadian regulation of glycogen synthase kinase 3β activity. (3) The effect of Cry1/Cry2 double KO seems to be different in mice than in cells: in these KO mice, a higher cytokine secretion was observed following LPS challenge, and this increased cytokine response can be prevented by blocking the NFκB pathway (Narasimamurthy et al. 2012). In this case, CRY action was not via repression of CLOCK/BMAL1 but through a regulation of adenylyl cyclase activity and protein kinase A-mediated phosphorylation of the p65 subunit of NFκB. (4) Another clock-related transcription factor, RORα, can control cytokine secretion by suppressing the nuclear entry of NFκB and positively regulating the expression of the inhibitor of NFκB, IκBα (Delerive et al. 2001). (5) SIRT1, a histone deacetylase whose activity varies with a circadian rhythm and that is known to regulate CLOCK/BMAL1 activity, was also demonstrated to impact on NFκB levels (Hwang et al. 2014). (6) Another mechanism seems to involve ubiquitin specific peptidase 2 (USP2) in TNF-α-induced NFκB signalling (Metzig et al. 2011). USP2 is a deubiquitinating enzyme whose mRNA levels oscillate along the day in various organs (Storch et al. 2002; Yan et al. 2008) and has been shown to regulate the clock proteins PER1, CRY1, and BMAL1 (Scoma et al. 2011; Tong et al. 2012; Yang et al. 2012). Thus, a surprisingly wide panel of regulatory mechanisms was found for a circadian regulation of NFκB activity, implicating various clock proteins and clock-controlled enzymes.

The reverse, a regulation of circadian rhythms by NFκB, also exists. At the molecular level, NFκB represses CLOCK/BMAL1-dependent genes (Bellet et al. 2012). For example, DBP mRNA is increased in cells KO for the NFκB subunit relB. In the SCN, NFκB is expressed in astrocytes and might mediate the effects of cytokines on central clock rhythms (Leone et al. 2006). For example, inhibition of NFκB activation with sulfasalazine blocks the phase-shifting of the clock that occurs in response to LPS (Marpegan et al. 2005). Finally, mice housed in constant darkness for 4 weeks exhibit depression-like behavior and elevated plasma IL-6. In the same model, clock gene expression is altered in the hippocampus. Interestingly, pharmacological inhibition of NFκB blunts the depression-like behavior, the elevation in IL-6, and the altered clock gene expression (Monje et al. 2011).

Other Possible Humoral Mediators of the Immune–Circadian Interaction

In addition to cytokines, the inflammatory response involves many other circulating molecules, which might act as cues to impact central and/or peripheral clock function.

Leptin

The white adipose tissue releases many molecules into the circulation upon LPS treatment (Fresno et al. 2011). This includes the energy-regulating adipokine leptin. Interestingly, leptin has immunomodulatory effects (Faggioni et al. 2001) and acts as a pro-inflammatory agent (Lago et al. 2007). Like most pro-inflammatory mediators, leptin rises in response to inflammatory signals (Aguilar-Valles et al. 2011; Sarraf et al. 1997) and is critical to the LPS-induced fever response (Harden et al. 2006; Luheshi et al. 1999; Sachot et al. 2004).

Some studies have shown a diurnal rhythm of leptin plasma levels, with a peak in the night in both humans and nocturnal rodents (Kalsbeek et al. 2001). Leptin treatment can strengthen the response of the SCN clock to light in mice (Mendoza et al. 2011). Applied in vitro, leptin phase advances the SCN clock (Prosser and Bergeron 2003) and it modulates the electrical properties of SCN neurons (Inyushkin et al. 2009). Mice lacking a functional leptin gene (ob/ob mice) have disrupted clock gene expression in both adipose tissue and liver (Ando et al. 2011), and rats with disrupted leptin signalling show tissue-specific alterations of clock gene expression (Motosugi et al. 2011). Even humans fed a high-fat diet have suppressed clock gene rhythms in adipose tissue, which parallels the disrupted leptin rhythms (Tahira et al. 2011). Similarly, in mice, a high-fat diet dampens the rhythmicity of clock gene expression in the adipose tissue, liver, and brainstem (Kaneko et al. 2009; Kohsaka et al. 2007). Although these studies do not show that the inflammatory role of leptin is involved in circadian rhythm regulation, it highlights possible interweaving between circadian rhythms, metabolism, and immune pathways.

Prostaglandin E2

Prostaglandin E2 (PGE2) can be produced in the brain and in the periphery. PGE2 is critical for the induction of fever in the thermoregulatory centers of the brain (Engblom et al. 2002; Milton and Wendlandt 1970). PGE2 is also upregulated in the periphery in response to LPS. Kupffer cells in the liver serve as a major source of this peripheral PGE2 induction (Li et al. 2006). This peripheral PGE2 induction is thought to contribute to the early cytokine-independent phase of LPS fever (Steiner et al. 2006).

The peripheral induction of PGE2 may influence peripheral clock gene expression. PGE2 treatment of mouse fibroblasts in vitro can induce rhythms of clock gene expression (Tsuchiya et al. 2005). In vivo, PGE2 injection can phase-shift clock gene expression rhythms in mouse liver, kidney, and heart, with no effects on central clock-controlled rhythms (Tsuchiya et al. 2005).

Glucocorticoids

Glucocorticoids (GCs) are steroid hormones synthesized in the adrenal gland cortex. The SCN clock is essential, via humoral (hypothalamic–pituitary–adrenal (HPA) axis) and neuronal pathways, for the very robust rhythmicity of GC synthesis and secretion under constant environmental conditions (Son et al. 2011). The local adrenal clock is also critical for the high-amplitude oscillations of this hormone (Oster et al. 2006; Son et al. 2008). GC levels in the circulation are highest in the early active phase (early day in humans, early night in nocturnal rodents) (Son et al. 2011). In humans, the phase of this rhythm opposes the pro-inflammatory rhythm, which has a peak at night. This is consistent with a well-known anti-inflammatory nature of GCs (Webster et al. 2002). Indeed, numerous studies have shown a role of GCs in regulating various cell types and tissues of the immune system (the reader is referred to Webster et al. 2002, for a review). High levels of GC in the circulation would mainly lead to suppressed immune responses and higher susceptibility to infection. On the contrary, suppression of GC levels would generally lead to exacerbated inflammatory responses (Webster et al. 2002). Consequently, the maintenance of coordinated GC rhythms is essential for health, and many inflammatory diseases are aggravated by abnormal GC rhythms (Carroll et al. 2008; Munck and Naray-Fejes-Toth 1992). For example, the mortality risk in patients with Cushing’s syndrome or Addison’s disease (with high and low circulating GC levels, respectively) is much higher when GC secretion is arrhythmic (Dallman et al. 2006).

GCs are potently upregulated by both LPS (Konsman et al. 2008) and turpentine oil injection (Turnbull et al. 2003), likely through the activation of the HPA axis by cytokines, in particular IL-6 (Petrovsky et al. 1998). Interestingly, this response to LPS varies across the day: the level of activation of the HPA axis is greater when LPS is administered at the beginning of the rest phase, when endogenous GC levels are low (Pollmacher et al. 1996).

Glucocorticoids (GCs) have also been shown to influence circadian clocks. Binding elements for GC receptors were found in the promoters of the clocks genes Per1 (Balsalobre et al. 2000; Fukuoka et al. 2005), Per2 (Cheon et al. 2013; So et al. 2009) and Rev-erbα (Torra et al. 2000). Accordingly, GC treatment acutely induces Per1 and Per2 expression in cultured cells (Balsalobre et al. 2000; Cheon et al. 2013), in vitro cultured lung slices (Gibbs et al. 2009) and in different organs upon injection in mice (Balsalobre et al. 2000). GCs can synchronize cellular circadian oscillators in vitro and in peripheral tissues in vivo (Balsalobre et al. 2000; Nagoshi et al. 2004; Son et al. 2008). Centrally, GC rhythms are necessary for PER2 protein rhythms in the limbic forebrain (Segall and Amir 2010b). As for the SCN master clock, the absence or low levels of GC receptors in the adult SCN (Balsalobre et al. 2000; Rosenfeld et al. 1993; Segall and Amir 2010b) probably explains the lack of effects of GC injection (Balsalobre et al. 2000; Segall and Amir 2010a) or adrenalectomy (Segall and Amir 2010b) on clock gene expression in the SCN. Overall, GCs are considered as likely candidates for mediating the resetting of the peripheral clocks and they were shown to regulate behavioral resetting, which is thought to be under the control of the SCN (Kiessling et al. 2010). These studies suggest that the differential induction of GCs in response to an immune challenge could impose time- and tissue-dependent regulation of clock gene expression.

In addition to the direct effects on clock genes via the GC receptor, GCs inhibit the action of NFκB by preventing binding to its target genes (Borghetti et al. 2009; Van Bogaert et al. 2010). Given the circadian rhythm of GC levels, this repression of NFκB probably occurs with a circadian rhythm too. Given the known effects of NFκB on clock genes (see above section on NFκB), it is thus possible that GCs, via the regulation of NFκB activity, impose a time dependence on the immune regulation of circadian clock gene expression.

Melatonin

Melatonin is a hormone synthesized and secreted by the pineal gland (Maronde and Stehle 2007). It is produced from serotonin as a result of a two-step synthesis pathway. Modification of serotonin by the enzyme arylalkylamine N-acetyltransferase (AA-NAT) is the rate-limiting step. AA-NAT is found at high levels in pinealocytes during the night (both in diurnal and nocturnal animals), and consequently, melatonin synthesis occurs mainly during the night. Melatonin has immunomodulatory effects (Carrillo-Vico et al. 2005), and the literature provides examples of both anti-inflammatory and pro-inflammatory roles, depending on the cell type and conditions (Mauriz et al. 2013). Melatonin influences the diurnal rhythms of leukocyte proliferation, cytokine production, and NK cell activity (del Gobbo et al. 1989; Drazen et al. 2001). In various inflammatory models, melatonin administration was shown to counter inflammation by lowering inducible nitric oxide synthase and cyclooxygenase-1/2 expression, PGE2 levels, and pro-inflammatory cytokine levels (Mauriz et al. 2013). On the other hand, in a mouse experimental model of arthritis, melatonin administration leads to decreased CRY1 protein and Cry1 mRNA levels and to worsened symptoms (Bang et al. 2012).

Melatonin was shown to inhibit LPS-induced NFκB activation in a microglial cell line, in turn inhibiting chemokine secretion and promoting the anti-inflammatory role of this hormone (Min et al. 2012). Pineal microglia respond to LPS and express TNF-α following the activation of the NFκB pathway (da Silveira Cruz-Machado et al. 2012). TNF-α then binds its receptor on pinealocytes to negatively regulate Aa-nat gene expression and melatonin production (Carvalho-Sousa et al. 2011). This repression seems to be part of a switch in the source of melatonin, from pinealocytes to immunocompetent cells (Markus et al. 2013). Upon inflammation, NFκB appears to be a key player both for the downregulation of AA-NAT in the pineal (as described above) and for its induction in immune cells, e.g., macrophages, leading to the secretion of melatonin by these cells (Muxel et al. 2012). Melatonin then acts in an autocrine fashion on macrophages themselves, to increase phagocytic activity. Interestingly, melatonin itself but also corticosterone cooperate to reduce macrophage-borne melatonin production upon recovery from inflammation (Markus et al. 2013). Melatonin and corticosterone also regulate NFκB in the pineal gland: in this organ, NFκB protein levels are rhythmic and melatonin inhibits NFκB activation (Cecon et al. 2010), while stress-induced plasma corticosterone leads to reduced NFκB nuclear levels in the hamster pineal gland (Ferreira et al. 2012).

Other examples exist of interplay between melatonin and GCs. Such an interplay was proposed to contribute to the aggravated morning inflammation in rheumatoid arthritis (RA). Pro-inflammatory cytokines such as IL-6 are upregulated in RA patients during the night and early morning (Cutolo et al. 2006). This nocturnal pro-inflammatory state was associated with increased melatonin levels at night and lower GC levels in the early morning. Indeed, if GC treatment is administered at the maximum pro-inflammatory peak in RA patients, then inflammation is greatly reduced (Jacobs and Bijlsma 2010). More generally, given the regulatory role of melatonin and GCs in inflammation, the interplay between their respective rhythms could contribute to the pro-inflammatory states induced by an acute inflammatory challenge. Given that GCs are time-dependently induced following an inflammatory stimulus, the shift in the balance of these two hormones may create altered pro-inflammatory states, accounting to the time-dependent variation in the immune response.

Coordination of Peripheral Clocks by Core Body Temperature Rhythms and Effects of Fever

The central clock of the SCN drives rhythms in core body temperature, which peaks during the active phase in both humans (light phase) and nocturnal rodents (dark phase). While the SCN network makes this central clock resistant to body temperature daily fluctuations, the body temperature rhythm was proposed to coordinate peripheral clocks (Buhr et al. 2010). Emulated physiological temperature rhythms can maintain rhythmicity of clock gene expression in cell culture and even shift rhythms to a new phase (Brown et al. 2002; Saini et al. 2012), but sudden temperature pulses have the capacity to synchronize cellular oscillators (Brown et al. 2002). This last observation suggests that the rapid change in temperature observed with fever onset could affect the phase of peripheral circadian clocks, or at least provoke a transient alteration of the clock-controlled rhythms in peripheral organs.

Heat-sensing and cold-sensing molecules might be the molecular links between temperature oscillations and clock gene rhythmicity. The expression of several heat-shock proteins (HSPs) is rhythmic in the liver (Kornmann et al. 2007). HSP rhythmicity is driven by heat-shock factor (HSF)1, a transcription factor whose peak DNA-binding activity presents a circadian rhythm in the liver (Reinke et al. 2008). Notably, Hsf1-deficient mice have a longer free-running period than WT mice (Reinke et al. 2008). Further, HSF1 is required for the quick synchronization of cells to simulated body temperature rhythms (Saini et al. 2012) or following a quick heat pulse (Tamaru et al. 2011). These results support an earlier study showing that HSF1 is required for resetting Per2 expression by temperature pulses in cell culture (Buhr et al. 2010). Interestingly, studies have supported a role for HSPs in modulating NFκB response to TNF-α or endotoxin challenge (Liu et al. 2010). The latter observation adds another molecular layer of interplay between clock genes, factors responsive to elevated temperature, and a key factor involved in inflammatory responses.

Other studies have focused on the cold-induced RNA-binding proteins CIRBP and RBM3. These proteins were found to bind the 3′ untranslated region of clock gene and clock-controlled gene mRNAs and to regulate their circadian expression (Liu et al. 2013; Morf et al. 2012). Interestingly, in mouse tissues, mRNAs encoding cold-induced proteins are enriched during the day while mRNAs for HSPs reach peak levels during the night (Kornmann et al. 2007; Liu et al. 2013). This fits well with the circadian rhythm of body temperature in these nocturnal rodents (higher body temperature at night, or active period).

It was shown in both humans (Pollmacher et al. 1996) and rodents (Luker et al. 2000; Sugimoto et al. 1996) that the time of day of endotoxin treatment does not affect the absolute magnitude of fever induction. Similarly, fever induction following turpentine oil injection is relatively independent of the time of treatment (Westfall et al. 2013). In contrast, the local temperature increase in the brain is sensitive to the time of day of endotoxin treatment (Mathias et al. 2000). Despite the time independence of fever magnitude in peripheral tissues, it is possible that the kinetics of fever induction may change according to the time of day of endotoxin challenge. Altogether, the rapid changes in temperature induced by endotoxin treatment may cause time-dependent changes in peripheral clock gene expression. This time dependency might be due to the time-dependent rate of fever induction or by variation across the day of the activation of heat- or cold-responsive mechanisms.

Neuronal Connections Within the Immune–Circadian Interaction

An inflammatory challenge in the periphery can directly signal the central febrile mechanisms through both the sympathetic (SNS) and parasympathetic (PNS) nervous systems (Hori et al. 1995). Likewise, both the SNS and PNS can mediate signals to individual peripheral organs (Esquifino and Cardinali 1994; Hori et al. 1995). This communication loop is gated at several key points by the circadian system and could explain some of the time-dependent effects of the immune response.

LPS imparts an early fever response, which cannot be solely explained by the upregulation of humoral factors. It is possible that the local tissue-specific upregulation of cytokines activate vagal afferents (Mignini et al. 2003), which in turn activate fever pathways in the brain (Watkins et al. 1995). For example, vagal afferents in the liver activate the secretion of noradrenaline in the hypothalamus, induce prostaglandin release, and consequently fever (Sehic and Blatteis 1996). Correspondingly, both IL-1 receptor antagonist and IL-1β were shown to directly interact with vagal afferents (Goehler et al. 1997; Niijima 1996).

The SCN is intimately involved in the neural pathways regulating the immune response. In particular, the SCN is heavily interconnected with the paraventricular nucleus and the arcuate nucleus, two regions involved in peripheral circadian entrainment and immune function (Kalsbeek and Buijs 2002; Kalsbeek et al. 2006). The projections of the SCN to the key febrile centers (e.g., the preoptic anterior hypothalamic area) and the circadian regulation imposed on these centers through circadian factors such as leptin create additional levels of circadian control on immune neuronal signalling (Buijs et al. 2003). Of note though, there has still been no report on the effects of SCN lesion on the inflammatory response.

Autonomic afferents to peripheral organs play a role in the circadian regulation of the immune response. Vagal connections to peripheral immune-regulating tissues inhibit the release of cytokines, thereby controlling the magnitude of the immune response (Borovikova et al. 2000; Czura et al. 2003). One study found that the norepinephrine content in the rat spleen was rhythmic. When connections to the spleen were severed, the rhythms in cytokines and cytolytic factors of splenocytes and NK cells were disrupted along with the rhythmicity of Bmal1 and Per2 (Logan et al. 2011). Furthermore, adrenaline treatment on hepatic tissue slices acutely induced Per1, while daily treatment entrained liver rhythms in vivo in SCN-lesioned mice (Terazono et al. 2003). Also, vagal afferents were found to be essential for clock gene rhythmicity in the lung (Bando et al. 2007). The PNS and SNS connections to the adrenal gland are particularly important for the regulation of GC secretion (Buijs et al. 2003; Ishida et al. 2005). This is an important connection because as we noted above, GCs are important regulators of both the peripheral circadian response and immune regulation. Interestingly, some of the rhythmic humoral cues described above actually gate the immune-activated autonomic connection. For example, PGE2 can activate the vagus nerve in the periphery, as there is a large enrichment of PGE2 receptors on the vagal afferents in the abdominal compartment (Ek et al. 1998).

Conclusion

The dialog between the innate immune response and the endogenous circadian system occurs at multiple levels, due to the large overlap between these systems (Figs. 1, 2). The rhythmicity in cytokines and humoral factors including leptin, PGE2, GCs, and melatonin can potentially time the immune response. This in turn leads to specific changes in clock-controlled events. Further, the direct neuronal connections from the brain to the periphery may impose fast tissue-specific modifications in circadian clocks in conditions of inflammation. It is likely that no single factor can be coined as “the” mediator of the circadian–immune cross talk alone. Instead, various factors are likely to be involved, in a context- and tissue-dependent manner. Nevertheless, the prominence of the connections between these two key physiological systems underscores the importance of unravelling the mechanism involved. This will allow understanding on how infection and inflammation can affect biological rhythms and vice versa. At the same time, and more broadly, this research will provide a model for the circadian control of physiology. In the context of disease, the diurnal changes in the symptoms of different medical conditions such as RA or sepsis, and the higher incidence of various diseases (e.g., cancer) upon circadian disruption, altogether imply that the research on the reciprocal regulation of circadian clocks and inflammatory pathways will also have important implications for disease understanding and treatment.

Notes

Acknowledgments

The authors thank the members of N. Cermakian’s laboratory for discussions. This work was funded by a Canadian Institutes for Health Research grant (N. Cermakian), a graduate scholarship from the Fonds de recherche du Québec-Santé (FRQS) (S. Westfall) and a salary award from the FRQS (N. Cermakian).

Conflict of interest

The authors have no competing financial interests in relation to the presented article.

References

  1. Abo T, Kawate T, Itoh K et al (1981) Studies on the bioperiodicity of the immune response. I. Circadian rhythms of human T, B, and K cell traffic in the peripheral blood. J Immunol 126:1360–1363PubMedGoogle Scholar
  2. Ackermann K, Revell VL, Lao O et al (2012) Diurnal rhythms in blood cell populations and the effect of acute sleep deprivation in healthy young men. Sleep 35:933–940PubMedCentralPubMedGoogle Scholar
  3. Adams KL, Castanon-Cervantes O, Evans JA et al (2013) Environmental circadian disruption elevates the IL-6 response to lipopolysaccharide in blood. J Biol Rhythms 28:272–277PubMedGoogle Scholar
  4. Aguilar-Valles A, Jung S, Poole S et al (2011) Leptin and interleukin-6 alter the function of mesolimbic dopamine neurons in a rodent model of prenatal inflammation. Psychoneuroendocrinology 37:956–969PubMedGoogle Scholar
  5. Ando H, Kumazaki M, Motosugi Y et al (2011) Impairment of peripheral circadian clocks precedes metabolic abnormalities in ob/ob mice. Endocrinology 152:1347–1354PubMedGoogle Scholar
  6. Arjona A, Sarkar DK (2005) Circadian oscillations of clock genes, cytolytic factors, and cytokines in rat NK cells. J Immunol 174:7618–7624PubMedGoogle Scholar
  7. Arjona A, Sarkar DK (2006) Evidence supporting a circadian control of natural killer cell function. Brain Behav Immun 20:469–476PubMedGoogle Scholar
  8. Arjona A, Sarkar DK (2008) Are circadian rhythms the code of hypothalamic–immune communication? Insights from natural killer cells. Neurochem Res 33:708–718PubMedGoogle Scholar
  9. Balsalobre A, Brown SA, Marcacci L et al (2000) Resetting of circadian time in peripheral tissues by glucocorticoid signaling. Science 289:2344–2347PubMedGoogle Scholar
  10. Bando H, Nishio T, van der Horst GT et al (2007) Vagal regulation of respiratory clocks in mice. J Neurosci 27:4359–4365PubMedGoogle Scholar
  11. Bang J, Chang HW, Jung HR et al (2012) Melatonin attenuates clock gene Cryptochrome1, which may aggravates mouse anti-type II collagen antibody-induced arthritis. Rheumatol Int 32:379–385PubMedGoogle Scholar
  12. Bellet MM, Zocchi L, Sassone-Corsi P (2012) The RelB subunit of NFκB acts as a negative regulator of circadian gene expression. Cell Cycle 11:3304–3311PubMedCentralPubMedGoogle Scholar
  13. Bellet MM, Deriu E, Liu JZ et al (2013) Circadian clock regulates the host response to Salmonella. Proc Natl Acad Sci USA 110:9897–9902PubMedCentralPubMedGoogle Scholar
  14. Benedict C, Dimitrov S, Marshall L et al (2007) Sleep enhances serum interleukin-7 concentrations in humans. Brain Behav Immun 21:1058–1062PubMedGoogle Scholar
  15. Besedovsky L, Born J, Lange T (2014) Endogenous glucocorticoid receptor signaling drives rhythmic changes in human T-cell subset numbers and the expression of the chemokine receptor CXCR4. FASEB J 28:67–75PubMedGoogle Scholar
  16. Beynon AL, Coogan AN (2010) Diurnal, age, and immune regulation of interleukin-1β and interleukin-1 type 1 receptor in the mouse suprachiasmatic nucleus. Chronobiol Int 27:1546–1563PubMedGoogle Scholar
  17. Boggio VI, Castrillon PO, Perez Lloret S et al (2003) Cerebroventricular administration of interferon-gamma modifies locomotor activity in the golden hamster. Neurosignals 12:89–94PubMedGoogle Scholar
  18. Bollinger T, Leutz A, Leliavski A et al (2011) Circadian clocks in mouse and human CD4+ T cells. Plos One 6:e29801PubMedCentralPubMedGoogle Scholar
  19. Borghetti P, Saleri R, Mocchegiani E et al (2009) Infection, immunity and the neuroendocrine response. Vet Immunol Immunopathol 130:141–162PubMedGoogle Scholar
  20. Born J, Lange T, Hansen K et al (1997) Effects of sleep and circadian rhythm on human circulating immune cells. J Immunol 158:4454–4464PubMedGoogle Scholar
  21. Borovikova LV, Ivanova S, Zhang M et al (2000) Vagus nerve stimulation attenuates the systemic inflammatory response to endotoxin. Nature 405:458–462PubMedGoogle Scholar
  22. Brown SA, Zumbrunn G, Fleury-Olela F et al (2002) Rhythms of mammalian body temperature can sustain peripheral circadian clocks. Curr Biol 12:1574–1583PubMedGoogle Scholar
  23. Buhr ED, Yoo SH, Takahashi JS (2010) Temperature as a universal resetting cue for mammalian circadian oscillators. Science 330:379–385PubMedCentralPubMedGoogle Scholar
  24. Buijs RM, la Fleur SE, Wortel J et al (2003) The suprachiasmatic nucleus balances sympathetic and parasympathetic output to peripheral organs through separate preautonomic neurons. J Comp Neurol 464:36–48PubMedGoogle Scholar
  25. Carlson DE, Chiu WC (2008) The absence of circadian cues during recovery from sepsis modifies pituitary-adrenocortical function and impairs survival. Shock 29:127–132PubMedGoogle Scholar
  26. Carrillo-Vico A, Guerrero JM, Lardone PJ et al (2005) A review of the multiple actions of melatonin on the immune system. Endocrine 27:189–200PubMedGoogle Scholar
  27. Carroll T, Raff H, Findling JW (2008) Late-night salivary cortisol measurement in the diagnosis of Cushing’s syndrome. Nat Clin Pract Endocrinol Metab 4:344–350PubMedGoogle Scholar
  28. Carvalho-Sousa CE, da Silveira Cruz-Machado S, Tamura EK et al (2011) Molecular basis for defining the pineal gland and pinealocytes as targets for tumor necrosis factor. Front Endocrinol 2:10Google Scholar
  29. Castanon-Cervantes O, Wu M, Ehlen JC et al (2010) Dysregulation of inflammatory responses by chronic circadian disruption. J Immunol 185:5796–5805PubMedCentralPubMedGoogle Scholar
  30. Cavadini G, Petrzilka S, Kohler P et al (2007) TNF-α suppresses the expression of clock genes by interfering with E-box-mediated transcription. Proc Natl Acad Sci USA 104:12843–12848PubMedCentralPubMedGoogle Scholar
  31. Cecon E, Fernandes PA, Pinato L et al (2010) Daily variation of constitutively activated nuclear factor kappa B (NFκB) in rat pineal gland. Chronobiol Int 27:52–67PubMedGoogle Scholar
  32. Cheon S, Park N, Cho S et al (2013) Glucocorticoid-mediated Period2 induction delays the phase of circadian rhythm. Nucleic Acids Res 41:6161–6174PubMedCentralPubMedGoogle Scholar
  33. Cutolo M, Sulli A, Pizzorni C et al (2006) Circadian rhythms: glucocorticoids and arthritis. Ann NY Acad Sci 1069:289–299PubMedGoogle Scholar
  34. Czura CJ, Friedman SG, Tracey KJ (2003) Neural inhibition of inflammation: the cholinergic anti-inflammatory pathway. J Endotoxin Res 9:409–413PubMedGoogle Scholar
  35. da Silveira Cruz-Machado S, Pinato L, Tamura EK et al (2012) Glia–pinealocyte network: the paracrine modulation of melatonin synthesis by tumor necrosis factor (TNF). Plos One 7:e40142PubMedCentralPubMedGoogle Scholar
  36. Dallman MF, Pecoraro NC, La Fleur SE et al (2006) Glucocorticoids, chronic stress, and obesity. Prog Brain Res 153:75–105PubMedGoogle Scholar
  37. Dantzer R (2001) Cytokine-induced sickness behavior: mechanisms and implications. Ann NY Acad Sci 933:222–234PubMedGoogle Scholar
  38. del Gobbo V, Libri V, Villani N et al (1989) Pinealectomy inhibits interleukin-2 production and natural killer activity in mice. Int J Immunopharmacol 11:567–573PubMedGoogle Scholar
  39. Delerive P, Monte D, Dubois G et al (2001) The orphan nuclear receptor ROR alpha is a negative regulator of the inflammatory response. EMBO Rep 2:42–48PubMedCentralPubMedGoogle Scholar
  40. Depres-Brummer P, Bourin P, Pages N et al (1997) Persistent T lymphocyte rhythms despite suppressed circadian clock outputs in rats. Am J Physiol 273:R1891–R1899PubMedGoogle Scholar
  41. Dibner C, Schibler U, Albrecht U (2010) The mammalian circadian timing system: organization and coordination of central and peripheral clocks. Annu Rev Physiol 72:517–549PubMedGoogle Scholar
  42. Dimitrov S, Benedict C, Heutling D et al (2009) Cortisol and epinephrine control opposing circadian rhythms in T cell subsets. Blood 113:5134–5143PubMedCentralPubMedGoogle Scholar
  43. Drazen DL, Bilu D, Bilbo SD et al (2001) Melatonin enhancement of splenocyte proliferation is attenuated by luzindole, a melatonin receptor antagonist. Am J Physiol Regul Integr Comp Physiol 280:R1476–R1482PubMedGoogle Scholar
  44. Duguay D, Cermakian N (2009) The crosstalk between physiology and circadian clock proteins. Chronobiol Int 26:1479–1513PubMedGoogle Scholar
  45. Duhart JM, Leone MJ, Paladino N et al (2013) Suprachiasmatic astrocytes modulate the circadian clock in response to TNF-α. J Immunol 191:4656–4664PubMedGoogle Scholar
  46. Ek M, Kurosawa M, Lundeberg T et al (1998) Activation of vagal afferents after intravenous injection of interleukin-1β: role of endogenous prostaglandins. J Neurosci 18:9471–9479PubMedGoogle Scholar
  47. Engblom D, Ek M, Saha S et al (2002) Prostaglandins as inflammatory messengers across the blood–brain-barrier. J Mol Med 80:5–15PubMedGoogle Scholar
  48. Esquifino AI, Cardinali DP (1994) Local regulation of the immune response by the autonomic nervous system. Neuroimmunomodulation 1:265–273PubMedGoogle Scholar
  49. Esquifino AI, Chacon F, Cano P et al (2004) Twenty-four-hour rhythms of mitogenic responses, lymphocyte subset populations and amino acid content in submaxillary lymph nodes of growing male rats subjected to calorie restriction. J Neuroimmunol 156:66–73PubMedGoogle Scholar
  50. Faggioni R, Feingold KR, Grunfeld C (2001) Leptin regulation of the immune response and the immunodeficiency of malnutrition. FASEB J 15:2565–2571PubMedGoogle Scholar
  51. Ferreira ZS, Bothorel B, Markus RP et al (2012) Plasma corticosterone elevation inhibits the activation of nuclear factor kappa B (NFκB) in the Syrian hamster pineal gland. Stress 15:339–347PubMedGoogle Scholar
  52. Fortier EE, Rooney J, Dardente H et al (2011) Circadian variation of the response of T cells to antigen. J Immunol 187:6291–6300PubMedGoogle Scholar
  53. Fresno M, Alvarez R, Cuesta N (2011) Toll-like receptors, inflammation, metabolism and obesity. Arch Physiol Biochem 117:151–164PubMedGoogle Scholar
  54. Fukuoka Y, Burioka N, Takata M et al (2005) Glucocorticoid administration increases hPer1 mRNA levels in human peripheral blood mononuclear cells in vitro or in vivo. J Biol Rhythms 20:550–553PubMedGoogle Scholar
  55. Gibbs JE, Beesley S, Plumb J et al (2009) Circadian timing in the lung; a specific role for bronchiolar epithelial cells. Endocrinology 150:268–276PubMedGoogle Scholar
  56. Gibbs JE, Blaikley J, Beesley S et al (2012) The nuclear receptor REV-ERBα mediates circadian regulation of innate immunity through selective regulation of inflammatory cytokines. Proc Natl Acad Sci USA 109:582–587PubMedCentralPubMedGoogle Scholar
  57. Goehler LE, Relton JK, Dripps D et al (1997) Vagal paraganglia bind biotinylated interleukin-1 receptor antagonist: a possible mechanism for immune-to-brain communication. Brain Res Bull 43:357–364PubMedGoogle Scholar
  58. Guan Z, Vgontzas AN, Omori T et al (2005) Interleukin-6 levels fluctuate with the light–dark cycle in the brain and peripheral tissues in rats. Brain Behav Immun 19:526–529PubMedGoogle Scholar
  59. Haimovich B, Calvano J, Haimovich AD et al (2010) In vivo endotoxin synchronizes and suppresses clock gene expression in human peripheral blood leukocytes. Crit Care Med 38:751–758PubMedCentralPubMedGoogle Scholar
  60. Halberg F, Johnson EA, Brown BW et al (1960) Susceptibility rhythm to E. coli endotoxin and bioassay. Proc Soc Exp Biol Med 103:142–144PubMedGoogle Scholar
  61. Harden LM, du Plessis I, Poole S et al (2006) Interleukin-6 and leptin mediate lipopolysaccharide-induced fever and sickness behavior. Physiol Behav 89:146–155PubMedGoogle Scholar
  62. Hashiramoto A, Yamane T, Tsumiyama K et al (2010) Mammalian clock gene Cryptochrome regulates arthritis via proinflammatory cytokine TNF-α. J Immunol 184:1560–1565PubMedGoogle Scholar
  63. Hastings M, O’Neill JS, Maywood ES (2007) Circadian clocks: regulators of endocrine and metabolic rhythms. J Endocrinol 195:187–198PubMedGoogle Scholar
  64. Haus E, Smolensky MH (1999) Biologic rhythms in the immune system. Chronobiol Int 16:581–622PubMedGoogle Scholar
  65. Hayashi M, Shimba S, Tezuka M (2007) Characterization of the molecular clock in mouse peritoneal macrophages. Biol Pharm Bull 30:621–626PubMedGoogle Scholar
  66. Hori T, Katafuchi T, Take S et al (1995) The autonomic nervous system as a communication channel between the brain and the immune system. Neuroimmunomodulation 2:203–215PubMedGoogle Scholar
  67. Hrushesky WJ, Langevin T, Kim YJ et al (1994) Circadian dynamics of tumor necrosis factor alpha (cachectin) lethality. J Exp Med 180:1059–1065PubMedGoogle Scholar
  68. Hwang JW, Sundar IK, Yao H et al (2014) Circadian clock function is disrupted by environmental tobacco/cigarette smoke, leading to lung inflammation and injury via a SIRT1-BMAL1 pathway. FASEB J 28:176–194PubMedGoogle Scholar
  69. Inyushkin AN, Bhumbra GS, Dyball RE (2009) Leptin modulates spike coding in the rat suprachiasmatic nucleus. J Neuroendocrinol 21:705–714PubMedGoogle Scholar
  70. Ishida A, Mutoh T, Ueyama T et al (2005) Light activates the adrenal gland: timing of gene expression and glucocorticoid release. Cell Metab 2:297–307PubMedGoogle Scholar
  71. Jacobs JW, Bijlsma JW (2010) Modified release prednisone in patients with rheumatoid arthritis. Ann Rheum Dis 69:1257–1259PubMedGoogle Scholar
  72. Kalsbeek A, Buijs RM (2002) Output pathways of the mammalian suprachiasmatic nucleus: coding circadian time by transmitter selection and specific targeting. Cell Tissue Res 309:109–118PubMedGoogle Scholar
  73. Kalsbeek A, Fliers E, Romijn JA et al (2001) The suprachiasmatic nucleus generates the diurnal changes in plasma leptin levels. Endocrinology 142:2677–2685PubMedGoogle Scholar
  74. Kalsbeek A, Perreau-Lenz S, Buijs RM (2006) A network of (autonomic) clock outputs. Chronobiol Int 23:521–535PubMedGoogle Scholar
  75. Kaneko K, Yamada T, Tsukita S et al (2009) Obesity alters circadian expressions of molecular clock genes in the brainstem. Brain Res 1263:58–68PubMedGoogle Scholar
  76. Kawate T, Abo T, Hinuma S et al (1981) Studies of the bioperiodicity of the immune response. II. Co-variations of murine T and B cells and a role of corticosteroid. J Immunol 126:1364–1367PubMedGoogle Scholar
  77. Keller M, Mazuch J, Abraham U et al (2009) A circadian clock in macrophages controls inflammatory immune responses. Proc Natl Acad Sci USA 106:21407–21412PubMedCentralPubMedGoogle Scholar
  78. Kiessling S, Eichele G, Oster H (2010) Adrenal glucocorticoids have a key role in circadian resynchronization in a mouse model of jet lag. J Clin Invest 120:2600–2609PubMedCentralPubMedGoogle Scholar
  79. Kirsch S, Thijssen S, Alarcon Salvador S et al (2012) T-cell numbers and antigen-specific T-cell function follow different circadian rhythms. J Clin Immunol 32:1381–1389PubMedGoogle Scholar
  80. Kitoh Y, Ohmori M, Araki N et al (2005) Dosing-time-dependent differences in lipopolysaccharide-induced liver injury in rats. Chronobiol Int 22:987–996PubMedGoogle Scholar
  81. Kohsaka A, Laposky AD, Ramsey KM et al (2007) High-fat diet disrupts behavioral and molecular circadian rhythms in mice. Cell Metab 6:414–421PubMedGoogle Scholar
  82. Konsman JP, Veeneman J, Combe C et al (2008) Central nervous action of interleukin-1 mediates activation of limbic structures and behavioural depression in response to peripheral administration of bacterial lipopolysaccharide. Eur J Neurosci 28:2499–2510PubMedGoogle Scholar
  83. Kornmann B, Schaad O, Bujard H et al (2007) System-driven and oscillator-dependent circadian transcription in mice with a conditionally active liver clock. PLoS Biol 5:e34PubMedCentralPubMedGoogle Scholar
  84. Koyanagi S, Ohdo S (2002) Alteration of intrinsic biological rhythms during interferon treatment and its possible mechanism. Mol Pharmacol 62:1393–1399PubMedGoogle Scholar
  85. Koyanagi S, Suyama H, Kuramoto Y et al (2006) Glucocorticoid regulation of 24-h oscillation in interferon receptor gene expression in mouse liver. Endocrinology 147:5034–5040PubMedGoogle Scholar
  86. Kwak Y, Lundkvist GB, Brask J et al (2008) Interferon-gamma alters electrical activity and clock gene expression in suprachiasmatic nucleus neurons. J Biol Rhythms 23:150–159PubMedGoogle Scholar
  87. Lago F, Dieguez C, Gomez-Reino J et al (2007) Adipokines as emerging mediators of immune response and inflammation. Nat Clin Pract Rheumatol 3:716–724PubMedGoogle Scholar
  88. Lange T, Dimitrov S, Born J (2010) Effects of sleep and circadian rhythm on the human immune system. Ann NY Acad Sci 1193:48–59PubMedGoogle Scholar
  89. Lee JH, Sancar A (2011) Regulation of apoptosis by the circadian clock through NF-κB signaling. Proc Natl Acad Sci USA 108:12036–12041PubMedCentralPubMedGoogle Scholar
  90. Leone MJ, Marpegan L, Bekinschtein TA et al (2006) Suprachiasmatic astrocytes as an interface for immune–circadian signalling. J Neurosci Res 84:1521–1527PubMedGoogle Scholar
  91. Leone MJ, Marpegan L, Duhart JM et al (2012) Role of proinflammatory cytokines on lipopolysaccharide-induced phase shifts in locomotor activity circadian rhythm. Chronobiol Int 29:715–723PubMedGoogle Scholar
  92. Li Z, Perlik V, Feleder C et al (2006) Kupffer cell-generated PGE2 triggers the febrile response of guinea pigs to intravenously injected LPS. Am J Physiol Regul Integr Comp Physiol 290:R1262–R1270PubMedGoogle Scholar
  93. Liu J, Malkani G, Shi X et al (2006) The circadian clock Period 2 gene regulates gamma interferon production of NK cells in host response to lipopolysaccharide-induced endotoxic shock. Infect Immun 74:4750–4756PubMedCentralPubMedGoogle Scholar
  94. Liu J, Hong S, Feng Z et al (2010) Regulation of lipopolysaccharide-induced inflammatory response by heat shock protein 27 in THP-1 cells. Cell Immunol 264:127–134PubMedGoogle Scholar
  95. Liu Y, Hu W, Murakawa Y et al (2013) Cold-induced RNA-binding proteins regulate circadian gene expression by controlling alternative polyadenylation. Sci Rep 3:2054PubMedCentralPubMedGoogle Scholar
  96. Logan RW, Sarkar DK (2012) Circadian nature of immune function. Mol Cell Endocrinol 349:82–90PubMedGoogle Scholar
  97. Logan RW, Arjona A, Sarkar DK (2011) Role of sympathetic nervous system in the entrainment of circadian natural-killer cell function. Brain Behav Immun 25:101–109PubMedCentralPubMedGoogle Scholar
  98. Logan RW, Zhang C, Murugan S et al (2012) Chronic shift-lag alters the circadian clock of NK cells and promotes lung cancer growth in rats. J Immunol 188:2583–2591PubMedCentralPubMedGoogle Scholar
  99. Lu YC, Yeh WC, Ohashi PS (2008) LPS/TLR4 signal transduction pathway. Cytokine 42:145–151PubMedGoogle Scholar
  100. Luheshi G, Gardner JD, Rushforth DA et al (1999) Leptin actions on food intake and body temperature are mediated by IL-1. Proc Natl Acad Sci USA 96:7047–7052PubMedCentralPubMedGoogle Scholar
  101. Luker FI, Mitchell D, Laburn HP (2000) Fever and motor activity in rats following day and night injections of Staphylococcus aureus cell walls. Am J Physiol Regul Integr Comp Physiol 279:R610–R616PubMedGoogle Scholar
  102. Lundkvist GB, Robertson B, Mhlanga JD et al (1998) Expression of an oscillating interferon-gamma receptor in the suprachiasmatic nuclei. Neuroreport 9:1059–1063PubMedGoogle Scholar
  103. Markus RP, Cecon E, Pires-Lapa MA (2013) Immune–pineal axis: nuclear factor κB (NF-κB) Mediates the shift in the melatonin source from pinealocytes to immune competent cells. Int J Mol Sci 14:10979–10997PubMedCentralPubMedGoogle Scholar
  104. Maronde E, Stehle JH (2007) The mammalian pineal gland: known facts, unknown facets. Trends Endocrinol Metab 18:142–149PubMedGoogle Scholar
  105. Marpegan L, Bekinschtein TA, Costas MA et al (2005) Circadian responses to endotoxin treatment in mice. J Neuroimmunol 160:102–109PubMedGoogle Scholar
  106. Marpegan L, Leone MJ, Katz ME et al (2009) Diurnal variation in endotoxin-induced mortality in mice: correlation with proinflammatory factors. Chronobiol Int 26:1430–1442PubMedGoogle Scholar
  107. Mathias S, Schiffelholz T, Linthorst AC et al (2000) Diurnal variations in lipopolysaccharide-induced sleep, sickness behavior and changes in corticosterone levels in the rat. Neuroendocrinology 71:375–385PubMedGoogle Scholar
  108. Mauriz JL, Collado PS, Veneroso C et al (2013) A review of the molecular aspects of melatonin’s anti-inflammatory actions: recent insights and new perspectives. J Pineal Res 54:1–14PubMedGoogle Scholar
  109. Mendoza J, Lopez-Lopez C, Revel FG et al (2011) Dimorphic effects of leptin on the circadian and hypocretinergic systems of mice. J Neuroendocrinol 23:28–38PubMedGoogle Scholar
  110. Metzig M, Nickles D, Falschlehner C, Lehmann-Koch J, Straub BK, Roth W, Boutros M (2011) An RNAi screen identifies USP2 as a factor required for TNF-alpha-induced NF-kappaB signaling. Int J Cancer 129:607–618Google Scholar
  111. Mignini F, Streccioni V, Amenta F (2003) Autonomic innervation of immune organs and neuroimmune modulation. Auton Autacoid Pharmacol 23:1–25PubMedGoogle Scholar
  112. Milton AS, Wendlandt S (1970) A possible role for prostaglandin E1 as a modulator for temperature regulation in the central nervous system of the cat. J Physiol 207:76P–77PPubMedGoogle Scholar
  113. Min KJ, Jang JH, Kwon TK (2012) Inhibitory effects of melatonin on the lipopolysaccharide-induced CC chemokine expression in BV2 murine microglial cells are mediated by suppression of Akt-induced NF-κB and STAT/GAS activity. J Pineal Res 52:296–304PubMedGoogle Scholar
  114. Monje FJ, Cabatic M, Divisch I et al (2011) Constant darkness induces IL-6-dependent depression-like behavior through the NF-κB signaling pathway. J Neurosci 31:9075–9083PubMedGoogle Scholar
  115. Morf J, Rey G, Schneider K et al (2012) Cold-inducible RNA-binding protein modulates circadian gene expression posttranscriptionally. Science 338:379–383PubMedGoogle Scholar
  116. Motosugi Y, Ando H, Ushijima K et al (2011) Tissue-dependent alterations of the clock gene expression rhythms in leptin-resistant Zucker diabetic fatty rats. Chronobiol Int 28:968–972PubMedGoogle Scholar
  117. Motzkus D, Albrecht U, Maronde E (2002) The human PER1 gene is inducible by interleukin-6. J Mol Neurosci 18:105–109PubMedGoogle Scholar
  118. Munck A, Naray-Fejes-Toth A (1992) The ups and downs of glucocorticoid physiology. Permissive and suppressive effects revisited. Mol Cell Endocrinol 90:C1–C4PubMedGoogle Scholar
  119. Murphy BA, Vick MM, Sessions DR et al (2007) Acute systemic inflammation transiently synchronizes clock gene expression in equine peripheral blood. Brain Behav Immun 21:467–476PubMedGoogle Scholar
  120. Muxel SM, Pires-Lapa MA, Monteiro AW et al (2012) NF-κB drives the synthesis of melatonin in RAW 264.7 macrophages by inducing the transcription of the arylalkylamine-N-acetyltransferase (AA-NAT) gene. Plos One 7:e52010PubMedCentralPubMedGoogle Scholar
  121. Nagoshi E, Saini C, Bauer C et al (2004) Circadian gene expression in individual fibroblasts: cell-autonomous and self-sustained oscillators pass time to daughter cells. Cell 119:693–705PubMedGoogle Scholar
  122. Nakagawa H, Okumura N (2010) Coordinated regulation of circadian rhythms and homeostasis by the suprachiasmatic nucleus. Proc Jpn Acad Ser B Phys Biol Sci 86:391–409PubMedCentralPubMedGoogle Scholar
  123. Narasimamurthy R, Hatori M, Nayak SK et al (2012) Circadian clock protein cryptochrome regulates the expression of proinflammatory cytokines. Proc Natl Acad Sci USA 109:12662–12667PubMedCentralPubMedGoogle Scholar
  124. Nguyen KD, Fentress SJ, Qiu Y et al (2013) Circadian gene Bmal1 regulates diurnal oscillations of Ly6C(hi) inflammatory monocytes. Science 341:1483–1488PubMedGoogle Scholar
  125. Niijima A (1996) The afferent discharges from sensors for interleukin 1 beta in the hepatoportal system in the anesthetized rat. J Auton Nerv Syst 61:287–291PubMedGoogle Scholar
  126. Nygard M, Lundkvist GB, Hill RH et al (2009) Rapid nitric oxide-dependent effects of tumor necrosis factor-alpha on suprachiasmatic nuclei neuronal activity. Neuroreport 20:213–217PubMedGoogle Scholar
  127. O’Callaghan EK, Anderson ST, Moynagh PN et al (2012) Long-lasting effects of sepsis on circadian rhythms in the mouse. Plos One 7:e47087PubMedCentralPubMedGoogle Scholar
  128. Ohdo S, Koyanagi S, Suyama H et al (2001) Changing the dosing schedule minimizes the disruptive effects of interferon on clock function. Nat Med 7:356–360PubMedGoogle Scholar
  129. Oishi K, Sakamoto K, Okada T et al (1998) Antiphase circadian expression between BMAL1 and period homologue mRNA in the suprachiasmatic nucleus and peripheral tissues of rats. Biochem Biophys Res Commun 253:199–203PubMedGoogle Scholar
  130. Okada K, Yano M, Doki Y et al (2008) Injection of LPS causes transient suppression of biological clock genes in rats. J Surg Res 145:5–12PubMedGoogle Scholar
  131. Oster H, Damerow S, Kiessling S et al (2006) The circadian rhythm of glucocorticoids is regulated by a gating mechanism residing in the adrenal cortical clock. Cell Metab 4:163–173PubMedGoogle Scholar
  132. Palomba M, Bentivoglio M (2008) Chronic inflammation affects the photic response of the suprachiasmatic nucleus. J Neuroimmunol 193:24–27PubMedGoogle Scholar
  133. Petrovsky N, McNair P, Harrison LC (1998) Diurnal rhythms of pro-inflammatory cytokines: regulation by plasma cortisol and therapeutic implications. Cytokine 10:307–312PubMedGoogle Scholar
  134. Petrzilka S, Taraborrelli C, Cavadini G et al (2009) Clock gene modulation by TNF-α depends on calcium and p38 MAP kinase signaling. J Biol Rhythms 24:283–294PubMedGoogle Scholar
  135. Pollmacher T, Mullington J, Korth C et al (1996) Diurnal variations in the human host response to endotoxin. J Infect Dis 174:1040–1045PubMedGoogle Scholar
  136. Prosser RA, Bergeron HE (2003) Leptin phase-advances the rat suprachiasmatic circadian clock in vitro. Neurosci Lett 336:139–142PubMedGoogle Scholar
  137. Raetz CR, Whitfield C (2002) Lipopolysaccharide endotoxins. Annu Rev Biochem 71:635–700PubMedCentralPubMedGoogle Scholar
  138. Reinke H, Saini C, Fleury-Olela F et al (2008) Differential display of DNA-binding proteins reveals heat-shock factor 1 as a circadian transcription factor. Genes Dev 22:331–345PubMedCentralPubMedGoogle Scholar
  139. Rosenfeld P, van Eekelen JA, Levine S et al (1993) Ontogeny of corticosteroid receptors in the brain. Cell Mol Neurobiol 13:95–319Google Scholar
  140. Rossol M, Heine H, Meusch U et al (2011) LPS-induced cytokine production in human monocytes and macrophages. Crit Rev Immunol 31:379–446PubMedGoogle Scholar
  141. Sachot C, Poole S, Luheshi GN (2004) Circulating leptin mediates lipopolysaccharide-induced anorexia and fever in rats. J Physiol 561:263–272PubMedCentralPubMedGoogle Scholar
  142. Sadki A, Bentivoglio M, Kristensson K et al (2007) Suppressors, receptors and effects of cytokines on the aging mouse biological clock. Neurobiol Aging 28:296–305PubMedGoogle Scholar
  143. Saini C, Morf J, Stratmann M et al (2012) Simulated body temperature rhythms reveal the phase-shifting behavior and plasticity of mammalian circadian oscillators. Genes Dev 26:567–580PubMedCentralPubMedGoogle Scholar
  144. Sam S, Corbridge TC, Mokhlesi B et al (2004) Cortisol levels and mortality in severe sepsis. Clin Endocrinol 60:29–35Google Scholar
  145. Sarraf P, Frederich RC, Turner EM et al (1997) Multiple cytokines and acute inflammation raise mouse leptin levels: potential role in inflammatory anorexia. J Exp Med 185:171–175PubMedCentralPubMedGoogle Scholar
  146. Sato S, Sakurai T, Ogasawara J et al (2014) A circadian clock gene, REV-ERBα, modulates the inflammatory function of macrophages through the negative regulation of Ccl2 expression. J Immunol 192:407–417PubMedGoogle Scholar
  147. Scheiermann C, Kunisaki Y, Lucas D et al (2012) Adrenergic nerves govern circadian leukocyte recruitment to tissues. Immunity 37:290–301PubMedCentralPubMedGoogle Scholar
  148. Scoma HD, Humby M, Yadav G et al (2011) The de-ubiquitinylating enzyme, USP2, is associated with the circadian clockwork and regulates its sensitivity to light. Plos One 6:e25382PubMedCentralPubMedGoogle Scholar
  149. Segall LA, Amir S (2010a) Exogenous corticosterone induces the expression of the clock protein, PERIOD2, in the oval nucleus of the bed nucleus of the stria terminalis and the central nucleus of the amygdala of adrenalectomized and intact rats. J Mol Neurosci 42:176–182PubMedGoogle Scholar
  150. Segall LA, Amir S (2010b) Glucocorticoid regulation of clock gene expression in the mammalian limbic forebrain. J Mol Neurosci 42:168–175PubMedGoogle Scholar
  151. Sehic E, Blatteis CM (1996) Blockade of lipopolysaccharide-induced fever by subdiaphragmatic vagotomy in guinea pigs. Brain Res 726:160–166PubMedGoogle Scholar
  152. Silver AC, Arjona A, Walker WE et al (2012) The circadian clock controls Toll-like receptor 9-mediated innate and adaptive immunity. Immunity 36:251–261PubMedCentralPubMedGoogle Scholar
  153. So AY, Bernal TU, Pillsbury ML et al (2009) Glucocorticoid regulation of the circadian clock modulates glucose homeostasis. Proc Natl Acad Sci USA 106:17582–17587PubMedCentralPubMedGoogle Scholar
  154. Son GH, Chung S, Choe HK et al (2008) Adrenal peripheral clock controls the autonomous circadian rhythm of glucocorticoid by causing rhythmic steroid production. Proc Natl Acad Sci USA 105:20970–20975PubMedCentralPubMedGoogle Scholar
  155. Son GH, Chung S, Kim K (2011) The adrenal peripheral clock: glucocorticoid and the circadian timing system. Front Neuroendocrinol 32:451–465PubMedGoogle Scholar
  156. Spengler ML, Kuropatwinski KK, Comas M et al (2012) Core circadian protein CLOCK is a positive regulator of NF-κB-mediated transcription. Proc Natl Acad Sci USA 109:E2457–E2465PubMedCentralPubMedGoogle Scholar
  157. Steiner AA, Ivanov AI, Serrats J et al (2006) Cellular and molecular bases of the initiation of fever. Plos Biol 4:e284PubMedCentralPubMedGoogle Scholar
  158. Storch KF, Lipan O, Leykin I et al (2002) Extensive and divergent circadian gene expression in liver and heart. Nature 417:78–83PubMedGoogle Scholar
  159. Sugimoto N, Shido O, Sakurada S et al (1996) Day–night variations of behavioral and autonomic thermoregulatory responses to lipopolysaccharide in rats. Jpn J Physiol 46:451–456PubMedGoogle Scholar
  160. Sun Y, Yang Z, Niu Z et al (2006) MOP3, a component of the molecular clock, regulates the development of B cells. Immunology 119:451–460PubMedCentralPubMedGoogle Scholar
  161. Tahira K, Ueno T, Fukuda N et al (2011) Obesity alters the expression profile of clock genes in peripheral blood mononuclear cells. Arch Med Sci 7:933–940PubMedCentralPubMedGoogle Scholar
  162. Tamaru T, Hattori M, Honda K et al (2011) Synchronization of circadian Per2 rhythms and HSF1-BMAL1: CLOCK interaction in mouse fibroblasts after short-term heat shock pulse. Plos One 6:e24521PubMedCentralPubMedGoogle Scholar
  163. Terazono H, Mutoh T, Yamaguchi S et al (2003) Adrenergic regulation of clock gene expression in mouse liver. Proc Natl Acad Sci USA 100:6795–6800PubMedCentralPubMedGoogle Scholar
  164. Tong X, Buelow K, Guha A et al (2012) USP2a protein deubiquitinates and stabilizes the circadian protein CRY1 in response to inflammatory signals. J Biol Chem 287:25280–25291PubMedCentralPubMedGoogle Scholar
  165. Torra IP, Tsibulsky V, Delaunay F et al (2000) Circadian and glucocorticoid regulation of REV-ERBα expression in liver. Endocrinology 141:3799–3806PubMedGoogle Scholar
  166. Tsuchiya Y, Minami I, Kadotani H et al (2005) Resetting of peripheral circadian clock by prostaglandin E2. EMBO Rep 6:256–261PubMedCentralPubMedGoogle Scholar
  167. Turnbull AV, Prehar S, Kennedy AR et al (2003) Interleukin-6 is an afferent signal to the hypothalamo-pituitary-adrenal axis during local inflammation in mice. Endocrinology 144:1894–1906PubMedGoogle Scholar
  168. Vallabhapurapu S, Karin M (2009) Regulation and function of NF-κB transcription factors in the immune system. Annu Rev Immunol 27:693–733PubMedGoogle Scholar
  169. Van Bogaert T, De Bosscher K, Libert C (2010) Crosstalk between TNF and glucocorticoid receptor signaling pathways. Cytokine Growth Factor Rev 21:275–286PubMedGoogle Scholar
  170. Watkins LR, Goehler LE, Relton JK et al (1995) Blockade of interleukin-1 induced hyperthermia by subdiaphragmatic vagotomy: evidence for vagal mediation of immune–brain communication. Neurosci Lett 183:27–31PubMedGoogle Scholar
  171. Webster JI, Tonelli L, Sternberg EM (2002) Neuroendocrine regulation of immunity. Annu Rev Immunol 20:125–163PubMedGoogle Scholar
  172. Westfall S, Aguilar-Valles A, Mongrain V et al (2013) Time-dependent effects of localized inflammation on peripheral clock gene expression in rats. Plos One 8:e59808PubMedCentralPubMedGoogle Scholar
  173. Yamamura Y, Yano I, Kudo T et al (2010) Time-dependent inhibitory effect of lipopolysaccharide injection on Per1 and Per2 gene expression in the mouse heart and liver. Chronobiol Int 27:213–232PubMedGoogle Scholar
  174. Yamazaki S, Numano R, Abe M et al (2000) Resetting central and peripheral circadian oscillators in transgenic rats. Science 288:682–685PubMedGoogle Scholar
  175. Yan J, Wang H, Liu Y et al (2008) Analysis of gene regulatory networks in the mammalian circadian rhythm. Plos Comput Biol 4:e1000193PubMedCentralPubMedGoogle Scholar
  176. Yang Y, Duguay D, Bedard N et al (2012) Regulation of behavioral circadian rhythms and clock protein PER1 by the deubiquitinating enzyme USP2. Biol Open 1:789–801PubMedCentralPubMedGoogle Scholar
  177. Yoo SH, Yamazaki S, Lowrey PL et al (2004) PERIOD2:LUCIFERASE real-time reporting of circadian dynamics reveals persistent circadian oscillations in mouse peripheral tissues. Proc Natl Acad Sci USA 101:5339–5346PubMedCentralPubMedGoogle Scholar
  178. Yoshida K, Hashiramoto A, Okano T et al (2013) TNF-α modulates expression of the circadian clock gene Per2 in rheumatoid synovial cells. Scand J Rheumatol 42:276–280PubMedGoogle Scholar
  179. Yu X, Rollins D, Ruhn KA et al (2013) TH17 cell differentiation is regulated by the circadian clock. Science 342:727–730PubMedGoogle Scholar

Copyright information

© L. Hirszfeld Institute of Immunology and Experimental Therapy, Wroclaw, Poland 2014

Authors and Affiliations

  • Nicolas Cermakian
    • 1
  • Susan Westfall
    • 1
  • Silke Kiessling
    • 1
  1. 1.Laboratory of Molecular Chronobiology, Douglas Mental Health University InstituteMcGill UniversityMontrealCanada

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