Regulation of GDF-15, a distant TGF-β superfamily member, in a mouse model of cerebral ischemia
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- Schindowski, K., von Bohlen und Halbach, O., Strelau, J. et al. Cell Tissue Res (2011) 343: 399. doi:10.1007/s00441-010-1090-5
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GDF-15 is a novel distant member of the TGF-β superfamily and is widely distributed in the brain and peripheral nervous system. We have previously reported that GDF-15 is a potent neurotrophic factor for lesioned dopaminergic neurons in the substantia nigra, and that GDF-15-deficient mice show progressive postnatal losses of motor and sensory neurons. We have now investigated the regulation of GDF-15 mRNA and immunoreactivity in the murine hippocampal formation and selected cortical areas following an ischemic lesion by occlusion of the middle cerebral artery (MCAO). MCAO prominently upregulates GDF-15 mRNA in the hippocampus and parietal cortex at 3 h and 24 h after lesion. GDF-15 immunoreactivity, which is hardly detectable in the unlesioned brain, is drastically upregulated in neurons identified by double-staining with NeuN. NeuN staining reveals that most, if not all, neurons in the granular layer of the dentate gyrus and pyramidal layers of the cornu ammonis become GDF-15-immunoreactive. Moderate induction of GDF-15 immunoreactivity has been observed in a small number of microglial cells identified by labeling with tomato lectin, whereas astroglial cells remain GDF-15-negative after MCAO. Comparative analysis of the size of the infarcted area after MCAO in GDF-15 wild-type and knockout mice has failed to reveal significant differences. Together, our data substantiate the notion that GDF-15 is prominently upregulated in the lesioned brain and might be involved in orchestrating post-lesional responses other than the trophic support of neurons.
KeywordsGrowth/differentiation factor-15 Expression Hippocampus Cortex Occlusion of the middle cerebral artery Ischemia GDF-15 knockout Mouse (adult, male, C57BL/6)
Stroke is the third most common cause of death in industrialized countries. Despite intense research efforts, there is still no advisable therapy for most patients (Kidwell et al. 2001; Schäbitz and Fisher 2006). Neurotrophins and growth factors with a capacity to promote the survival and regeneration of lesioned neurons have been proposed as useful for the treatment of cerebral ischemia. Their protective potential in ischemic lesions has been shown in a variety of in vitro and animal model studies (Kawamata et al. 1997; Ma et al. 2001; Schäbitz and Fisher 2006; Schäbitz et al. 2001; Song et al. 2002; Sugimori et al. 2001; Wagner et al. 1999). Even so, the transfer of trophic molecules from the bench to the clinic is still in its infancy, involves many still unresolved problems, such as modes of delivery, and may include unexpected draw-backs, as previously shown for fibroblast growth factor-2 (FGF-2; Bogousslavsky et al. 2002).
A major obstacle in the development of rational therapies for stroke is the lack of a coherent understanding of the primary and secondary molecular scenarios elicited by the ischemic insult. This also applies to the still incomplete picture of the lesion-mediated regulation of growth factors; this is of particular importance in light of the accumulating evidence for the multiple synergies and contextual actions of many growth factors (cf. Peterziel et al. 2002).
Growth/differentiation factor-15 (GDF-15) is a novel member of the transforming growth factor (TGF)-β superfamily and has been cloned and characterized in our and several other laboratories (Böttner et al. 1999a, b; Strelau et al. 2000b); it is identical to macrophage-inhibitory cytokine-1 (MIC-1; Bauskin et al. 2000; Bootcov et al. 1997; Fairlie et al. 1999), which is found in macrophages, and to some other published sequences (Hromas et al. 1997; Lawton et al. 1997; Yokoyama-Kobayashi et al. 1997). GDF-15/MIC-1 is widely expressed by many epithelia of exocrine glands, e.g., the prostate, salivary, and mammary glands, in the placenta, airways, liver, intestinal epithelia, and in the S3 segment of nephrons (Böttner et al. 1999b). Its functions at these locations are enigmatic. In macrophages, GDF-15/MIC-1 is induced by proinflammatory cytokines such as tumor necrosis factor (TNF)-α, interleukin (IL)-1β, and IL-6, but not by interferon (IFN)-γ and lipopolysaccharide (Bootcov et al. 1997).
We have previously shown that GDF-15 is a potent neurotrophic factor in vitro and in vivo for embryonic and lesioned midbrain dopaminergic neurons (Strelau et al. 2000b). Analysis of the knockout has revealed progressive postnatal losses of motoneurons in the hindbrain and spinal cord, together with sensory neuron losses (Strelau et al. 2009). GDF-15 is dramatically upregulated in cryolesioned cortical neurons (Schober et al. 2001) and has also been shown to prevent the death of potassium-deprived cerebellar granule neurons by activating Akt and inhibiting constitutively active extracellular signal-regulated kinase (Subramaniam et al. 2003).
We show now that GDF-15 is upregulated in hippocampal and cortical neurons following the occlusion of the middle cerebral artery (MCAO) in mice; this further corroborates the notion that GDF-15 is a lesion-induced factor. Comparative analysis of the size of the infarcted area in GDF-15 wild-type and knockout mice has failed to reveal significant differences suggesting that GDF-15 is involved in orchestrating post-lesional responses other than the trophic support of neurons.
Materials and methods
Surgical procedures for MCAO
Adult male C57BL/6 mice (25–35 g) were used throughout this study. To induce a transient MCAO, mice were anesthetized with 1% Halothane in 33% O2 and 66% N2O. Rectal temperature was monitored continuously and maintained at 37±0.5°C by external heating. For laser Doppler measurements, the probe (P403; Perimed, Järfälla, Sweden) was placed 3 mm lateral and 6 mm posterior to the Bregma. Relative perfusion units were measured. The left carotid region was exposed through a midline skin incision. A 5-0 nylon suture (Ethilon, Norderstedt, Germany) with a blunted tip was inserted into the external carotid artery and advanced into the internal carotid until the laser Doppler signal decreased considerably. The suture was removed after 15 min unless indicated otherwise. In sham-operated mice no suture was inserted. After 3 h up to 9 days of reperfusion, mice were deeply anesthetized (Rompun/Ketanest), and perfused brains were removed. The neurological status of the mice was assessed according to Bederson et al. (1986). Contralateral motor deficits of the upper limb were considered as an effect of MCAO. Infarct volumes were determined after an occlusion time of 30 min. To measure the infarct size, we deeply reanesthetized mice and perfused them intracardially with Ringer solution at 24 h after surgery. The procedure for infarct detection by silver staining of coronal cryosections, quantification, and edema correction was as previously described (Herrmann et al. 2005).
Infarct volumes in growth/differentiation factor-15 knockout (GDF-15 ko) and wild-type control mice. No statistically significant difference was noted between the genotypes (t-test). The transient occlusion of the middle cerebral artery (MCAO) lasted 30 min. Values are expressed as means ± SEM
GDF-15 ko mice
Infarct volume (mm³)
Infarct volume (mm³)
A polycolonal antibody against a specific peptide sequence (HRTDSGVSLQTYDDL) of the C-terminus of the GDF-15 protein was raised in rabbit by Dr. J. Pineda (FZB Biotechnik GmbH, Berlin, Germany) and characterized as described (Schober et al. 2001). Coronal paraffin-embedded sections (4 μm thickness) were stained with this polyclonal antibody in phosphate-buffered saline (PBS). A biotinylated secondary antibody against rabbit IgG was detected by using streptavidin coupled to Cy-2 and Cy-3 (purchased from Vector Labs), respectively, as indicated. Neurons were identified by staining with α-neuron-specific nuclear protein (α-NeuN; Santa Cruz, USA), GFAP+-astrocytes by staining for glial fibrillary acidic protein (GFAP; Sigma, Germany), and microglial cells by staining with tomato lectin (Sigma). Sections were counterstained with the nuclear dye 4,6-diamidino-2-phenylindole (DAPI; Sigma).
In situ hybridization
Mice were perfused with saline followed by 4% paraformaldehyde (PFA). Brains were removed, postfixed overnight at 4°C, and then placed in 30% sucrose for cryoprotection, prior to being frozen on dry ice. Cryosections (20 μm) were cut on a cryostat and mounted on Superfrost slides. Non-radioactive in situ hybridization on cryosections and the preparation of digoxigenin-labeled probes for mouse GDF-15 were carried out as previously described (Ernsberger et al. 1997). Mouse GDF-15 (bp: 713-1392, accession code AF159571) was cloned from adult mouse brain cDNA by the polymerase chain reaction (PCR) by using a pGEMT vector system (Promega) following the manufacturer’s instructions. The plasmid was appropriately linearized and transcribed with SP6 and T7 for the antisense probe and sense control, respectively.
Reverse transcription with PCR
Ischemic brain tissue consisting of the ipsilateral hippocampal formation and thalamus and the ipsilateral ischemic cortex (all between Bregma +0.1 mm and −2.8 mm) were prepared from saline-perfused brains and immediately frozen on dry ice. Tissue was homogenized under liquid nitrogen, and RNA was extracted with Tri-Fast (PeqLab, Germany). Synthesis of cDNA was performed with 1 μg total RNA, reverse transcriptase from Moloney murine leukemia virus, and oligo-dT18 (all purchased from New England Labs, Germany). For qualitative PCR, equal amounts of cDNA were used in a group of PCRs with a set of primers to amplify β-actin (5′-primer: 5′-TCATGAAGTGTGACGTTGACATCCGT-3′ 3′-primer: 5′-CCTAGAAGCATTTGCGGTGCACGATG-3′) as a house-keeping-gene and a set of primers to amplify GDF-15 (5′-primer: 5′-CCGAGAGGACTCGAACTCAG-3′ 3′-primer: 5′-TAAGAACCACCGGGGTGTAG-3′). For quantitative PCR, serial dilutions of cDNA were amplified in parallel with primers for cyclophilin (5′-primer: 5′-ACCCCACCGTGTTCTTCGAC-3′; 3′-primer: 5′-CATTTGCCATGGACAAGATG-3′) as internal standards and GDF-15 (5′-primer: 5′-GGCTGCATGCCAACCA-3′; 3′-primer: 5′-TCTCACCTCTGGACTGAGTATTCC-3′) with the SYBR-Green-Kit (PE Biosystems, Germany) in a GeneAmp-Cycler equipped with GeneAmp 5700SDS software.
GDF-15 is upregulated in the ischemic core following transient MCAO
GDF-15 mRNA is increased in the hippocampal formation and retrosplenial/motor cortex of the ipsilateral hemisphere as early as 3 h post-MCAO
GDF-15 immunoreactivity is increased in the hippocampus and cerebral cortex of the ipsilateral hemisphere following transient MCAO
GDF-15 is predominantly expressed by neurons subsequent to MCAO
Comparison in GDF-15 wild-type and knockout mice fails to reveal significant differences in the size of the infarcted area following transient or permanent MCAO
To evaluate the effect of GDF-15 on the lesion size, we subjected GDF-15 knockout mice and wild-type controls to a transient 30-min MCAO and measured the neurological deficit and the infarct size at 24 h after MCAO. The genotypes differed neither in the infarct size nor in the neurological deficit (Table 1). Moreover, in a model of permanent MCAO, which leads to predominantly cortical infarcts, the infarct size was unaffected by the GDF-15 deficiency (Table 1).
The results of the present study allow GDF-15, a novel member of the TGF-β superfamily, to be added to the list of growth factors and cytokines that play a role in ischemic brain lesion (Buisson et al. 2003; Harvey et al. 2005; Lykissas et al. 2007; Wu 2005). GDF-15 was discovered in our laboratory by searching expressed sequence tag databases for conserved structural hallmarks of TGF-βs (Böttner et al. 1999a, 1999b). Independently, the gene was also cloned by several other groups in the search for genes involved in (1) macrophage activation (MIC-1; Bootcov et al. 1997; Fairlie et al. 1999), (2) placental functions (placental bone morphogenetic protein; Hromas et al. 1997), and (3) anti-inflammatory functions (non-steroidal anti-inflammatory drug activated gene 1; Baek et al. 2001). The rat, mouse, and human genes of GDF-15 that we have isolated by screening of genomic libraries are all composed of two exons and contain a single intron that interrupts the coding sequences at identical positions within the prepro-domain of the corresponding proteins. The predicted proteins contain the structural hallmarks of members of the TGF-β superfamily, including the seven conserved carboxy-terminal cysteine residues that form the cystine knot. GDF-15 is synthesized as a large precursor molecule, which is cleaved to yield the biologically active mature protein. Expression of the proteases involved has not been studied in sufficient detail. The orthologous molecules show the lowest sequence conservation of all members of the TGF-β superfamily (Böttner et al. 1999b).
Most groups studying GDF-15 have focused on its putative functions in various pathologies and cancer. These include such diverse roles as, e.g., GDF-15 as a biomarker for p53 pathway activation (Yang et al. 2003), serum concentrations of GDF-15 as a predictor of miscarriage (Tong et al. 2004), its identification as a novel downstream target of the AKT/GSK-3beta pathway (Yamaguchi et al. 2004), and its pro-apoptotic role in prostate cancer cells (Liu et al. 2003) and many other cancer cell types. With well over 300 publications on GDF-15 (medline: gdf15 or gdf-15) to date, the lack of any in-depth analyses of its physiological functions in cell-biological contexts and in organs in which it is highly and specifically expressed and localized is surprising. Interestingly, in the context of our present study, two companion articles (Kempf et al. 2006; Xu et al. 2006) have reported that GDF-15 is a cardioprotective factor that is rapidly upregulated in cardiomyocytes on ischemia/reperfusion and during other cardiovascular events triggering oxidative stress, including pressure overload, heart failure, and atherosclerosis. Together with our data on the regulation of GDF-15 in brain lesions, this suggests that GDF-15 can act as a lesion-induced factor in other systems that counteract the consequences of lesioning. The receptor(s) for GDF-15 is unknown and possibly not a member of the TGF-β and glial-cell-derived neurotrophic factor (GDNF) receptor families.
Although GDF-15 is widely and prominently expressed in many injured organs and exocrine glands, in liver, lung, placenta, and kidney, (cf. Böttner et al. 1999a), its levels of expression in the adult rat and mouse central nervous system (CNS) are relatively low (Schober et al. 2001; Strelau et al. 2000b). The site with the highest expression level is the choroid plexus, from which GDF-15 is secreted into the cerebrospinal fluid. Although GDF-15 mRNA and protein can be detected by RT-PCR and immunoblotting in every region of the unlesioned brain studied (Strelau et al. 2000b), expression levels are apparently below detectability by in situ hybridisation and immunohistochemistry. However, in the neonatal brain, GDF-15 can be found outside the choroid plexus, in the ventricular and subventricular layers of the striatum (Schober et al. 2001).
Brain lesions profoundly alter GDF-15 expression. This has been documented in a previous study in which we have investigated the regulation of GDF-15 mRNA and protein following cryolesion of the rat cortex (Schober et al. 2001). Since GDF-15 is highly expressed by macrophages (Fairlie et al. 1999; Schlittenhardt et al. 2004), a rise in expression was primarily expected for microglial cells. Interestingly, this was not the case, and neurons close to the lesion site, but also neurons presumably projecting to the lesioned area, were identified as the predominant site of the observed rise in GDF-15 mRNA and protein following the cryolesion (Schober et al. 2001).
The present study, which involves the use of an entirely unrelated CNS lesion paradigm, further supports the notion that neurons, rather than microglia, are the predominant site of the upregulation of GDF-15 subsequent to lesion. The significance of this upregulation is enigmatic as yet but might be sought in relation to a role in rescuing neurons or in executing cell death. Several members of the TGF-β family, but also non-TGF-βs, have been implicated in performing dual roles in activating survival and death pathways in neurons, depending on the activation of specific sets of receptors and the contextual presence of other growth factors. For example, TGF-β can not only promote the survival of midbrain dopaminergic neurons in vitro and in vivo (Farkas et al. 2003; Krieglstein et al. 1995), but also, when neutralized in vivo, prevent programmed neuron death suggesting a pro-apoptotic function (Krieglstein et al. 2000). This also applies to GDF-15, for which anti- and proapoptic roles have been described (Baek et al. 2001; Liu et al. 2003; Strelau et al. 2000b; Subramaniam et al. 2003). TGF-β is well established as requiring additional factors for its neurotrophic actions, such as FGF-2 (Krieglstein et al. 1998c), GDNF (Krieglstein et al. 1998b; Schober et al. 1999, 2007), ciliary neurotrophic factor and neurotrophins (Krieglstein et al. 1998a). Whether this also applies to its pro-apoptotic roles is not known. With regard to GDF-15, any putative synergistically acting molecules, if required, still need to be identified. The molecular basis of the synergy of TGF-β with GDNF has been elucidated in greater detail. TGF-β apparently has the capacity to increase the insertion of a lipid-anchored co-receptor of GDNF, viz., GFRα1, into the plasma membrane (Peterziel et al. 2002, 2007), thereby enabling GDNF to activate its compound receptor GFRα1 and c-ret. Whether similar mechanisms are also activated by GDF-15 as a putative synergistic partner remain to be investigated. Thus, as shown in the present study, the expression of GDF-15 elicited in lesioned neurons is not overtly indicative of their protection or of the activation of death pathways. Although the infarct size in the GDF-15 knockout mice is not clearly different from that in GDF-15 wild-type mice, future studies using GDF-15 deficient mice (Strelau et al. 2009) can be expected to assign more detailed roles to GDF-15 in the orchestration of responses to brain lesions, possibly with prospects for using it as a target for therapeutic strategies.
We thank Ulla Hinz, Nicole Karch, and Elisabeth Specht-Delius for skilful technical assistance.
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