Administration of α-Galactosylceramide Improves Adenine-Induced Renal Injury
- 32 Downloads
Natural killer T (NKT) cells are a subset of lymphocytes that reacts to glycolipids presented by CD1d. Invariant NKT cells (iNKT) correspond to >90% of the total population of NKTs and reacts to a-galactosylceramide (αGalCer). αGalCer promotes a complex mixture of Th1 and Th2 cytokines, as interferon (IFN)-γ and interleukin (IL)-4. NKT cells and IFN-γ are known to participate in some models of renal diseases, but further studies are still necessary to elucidate their mechanisms. The aim of our study was to analyze the participation of iNKT cells in an experimental model of tubule-interstitial nephritis. We used 8-wk-old C57BL/6j, Jα18KO and IFN-γKO mice. They were fed a 0.25% adenine diet for 10 d. Both adenine-fed wild-type (WT) and Jα18KO mice exhibited renal dysfunction, but adenine-fed Jα18KO mice presented higher expression of kidney injury molecule-1 (KIM-1), tumor necrosis factor (TNF)-α and type I collagen. To analyze the role of activated iNKT cells in our model, we administered αGalCer in WT mice during adenine ingestion. After αGalCer injection, we observed a significant reduction in serum creatinine, proinflammatory cytokines and renal fibrosis. However, this improvement in renal function was not observed in IFN-γKO mice after αGalCer treatment and adenine feeding, illustrating that this cytokine plays a role in our model. Our findings may suggest that IFN-γ production is one of the factors contributing to improved renal function after αGalCer administration
Chronic kidney diseases (CKDs) are progressive scarring conditions characterized by a decrease in renal function over time affecting millions of people worldwide. A common final pathway of CKD is tubule-interstitial fibrosis, caused by excessive extracellular matrix deposition after chronic insults (1,2).
Independently of which renal compartment is affected, an inflammatory process is usually present in kidney diseases, and such a process can be resumed in some steps. First, a physical or chemical injury (for example, hypertension, drugs and obstruction) may cause a release of inflammatory mediators, which recruit inflammatory cells to the site. Such an inflammatory process affects tubular cells and may lead to apoptosis, necrosis or activation of interstitial fibroblasts, which produce collagens leading to a fibrotic scar (3, 4, 5).
In 1985, Yokozawa et al. (6) demonstrated that an excessive intake of adenine would lead to renal injury. Adenine is produced endogenously but its long-term ingestion results in 2,8-dihydrox-yadenine precipitation inside the renal tubules, leading to the formation of kidney stones, with extensive tubular dilation, inflammation, necrosis and fibrosis. The inflammatory process in this model is known to comprise the activation of toll-like receptors, inflammasome and nuclear factor (NF)-κB (2,7, 8, 9).
Furthermore, the involvement of immune cells is also a central step in the development of renal diseases. Various cell types infiltrate the kidney during the inflammatory process, for example, neutrophils, macrophages, T cells and others. A distinct subtype of T cells, called natural killer T (NKT) cells, might also be present in some kidney diseases.
NKT cells constitute a distinct population of lymphocytes found at low frequency (<1% in the peripheral blood of mice and humans) and characterized by their reactivity to glycolipids presented by CD1d, a molecule similar to MHC class I (10). Two major subtypes of NKT cells are currently recognized: type I and type II (11,12). Type I NKT cells, also called invariant NKT (iNKT), express a T-cell receptor (TCR) with a canonical rearrangement formed by a constant α chain (Vα14Jα18 in mice and Vα24Jα18 in humans) paired with a strict repertoire of β chains (Vβ8, Vβ7, Vβ2 in mice and Vβ11 in humans). iNKT cells correspond to >90% of the total population of NKT and react to the glycolipid α-galactosylceramide (αGalCer, also called KRN7000) and its analogs. αGalCer is a potent activator of both human and murine NKT cells and promotes a complex mixture of Th1 and Th2 cytokines, with an explosive release of interleukin (IL)-4 and large quantities of interferon (IFN)-γ (13, 14, 15).
IFN-γ is a potent cytokine with important and distinct functions. It is essential to host protection against intracellular pathogens but it can also contribute to autoimmunity (16). Thus, IFN-γ has different roles in inflammation and immune regulation depending on the conditions and influences from the microenvironment.
Since the role of NKT cell, and its cytokines (for example, IFN-γ), in renal diseases is still not fully elucidated, we aimed to analyze the involvement of these cells in an experimental model of tubule-interstitial nephritis.
Materials and Methods
We used male C57BL/6J, Jα18KO and IFN-γKO mice, 8–10 wks old. The Jα18KO mice were a gift from Dr. Masaru Taniguchi at the RIKEN Research Center for Allergy and Immunology (Japan) (17). All mice were kept in well-controlled animal housing facilities and had free access to water and food. Animals were provided by the animal facility of the Center for Development of Experimental Models for Medicine and Biology (CEDEME-UNIFESP, São Paulo, Brazil). All animal experiments were performed according to the Ethics Committee of the Federal University of São Paulo (number 2010/1517).
Tubule-Interstitial Nephritis Induction
To induce tubule-interstitial nephritis (TIN), mice were fed a diet containing 0.25% adenine (Rhoster) ad libitum for 10 d (8). Control mice were fed the standard diet. Blood and kidney samples were collected for analysis at d 4 and 10. Serum creatinine was measured by Jaffé’s modified method by using commercially purchased kits (Creatinine Kit, Labtest). Serum samples were deproteinizated before the colorimetric assay. NGAL (neutrophil gelatinase-associated lipocalin) (18) was measured in kidney tissue extract by using the commercially purchased kit Mouse NGAL ELISA Kit (BIOPORTO Diagnostics) according to the manufacturer’s protocol. NGAL is a type 1 acute phase protein that is upregulated in mouse kidney cells after some virus infection and in postischemic and nephrotoxic injury (19, 20, 21).
Another parameter used to assess TIN induction was kidney injury molecule-1 (KIM-1) mRNA expression. KIM-1 is a transmembrane protein that has been described to be highly expressed in the kidney after ischemia (22).
C57BL/6J wild-type (WT) and IFN-γKO mice were injected intraperitoneally with 5 µg αGalCer in 200 µL phosphate-buffered saline (PBS) + 0.5% polysorbate-20. αGalCer is a potent activator of both murine and human iNKT cells and induces the production of a complex mixture of Th1 and Th2 cytokines (14). αGalCer was obtained from Alexis Biochemicals, and it was initially solubilized in chloroform:methanol (2:1) to make aliquots. Solvent was removed from the aliquots by drying in nitrogen atmosphere; for use, the glycolipid was then resuspended to PBS + 0.5% polysorbate-20 and sonicated for 90 min at 60°C.
Quantitative Real-Time Polymerase Chain Reaction
Total RNA was extracted from a kidney section by using TRIzol Reagent (Invitrogen). First-strand cDNAs were synthesized using the Moloney murine leukemia virus (M-MLV) reverse-transcriptase kit (Promega). Real-time polymerase chain reaction (PCR) was performed on a GeneAmp 7300 Sequence Detection System (Applied Biosystems) by using SYBR Green, TaqMan Gene expression assays (Applied Biosystems) and PrimeTime® qPCR primers (Integrated DNA Technologies). Messenger RNA expression for each signal was calculated by using the delta threshold cycle (ΔCt) procedure. Hypoxanthine-guanine phosphoribosyltransferase (HPRT) was used as a reference gene. The primer sets are summarized in Supplementary Tables S1 and S2. Samples were run in triplicate. The relative expression amounts of the target mRNA to HPRT were calculated with the following equations. Relative expression level of the target mRNA = 2−ΔΔCt.
Formalin-fixed, paraffin-embedded kidney sections were deparaffinized and stained with Sirius red for histological analysis. Renal tissues were then visualized under polarized light, and the percentage of cortex fibrosis was quantified by using the ImageJ software.
A histopathologist, unaware of the type of treatment, evaluated histological changes semiquantitatively. Twenty fields per kidney at 200× magnification were examined for tubular injury by using a semiquantitative scale (23). Scores were assigned according to the percentage of cortical tubules having alterations, as follows: 0.0%; 1, unchanged, <10%; 2, slight change, 10–25%; 3, moderate alteration, 26–75%; or 4, intense alteration, >75%.
Immunohistochemistry for Fibroblast-Specific Protein-1 (FSP-1) and α-Smooth Muscle Actin (α-SMA)
Renal interstitial fibrosis is also characterized by excessive deposition of extracellular matrix and accumulation of fibroblasts (24). Although other cell types may be involved, the fibroblasts can be considered as key mediators of renal fibrosis (25,26). Given the important role of fibroblasts, we analyzed in our study the FSP-1 expression in renal tissue and also α-SMA, which is related to the contractile function acquired by the myofibroblasts during the fibrotic process.
Thin sections of the renal tissue were deparaffinized and dehydrated by a series of xylene and alcohol washes. For antigen retrieval, sections were microwaved (10 min) in Tris-EDTA (ethylenediaminetetraacetic acid) buffer. Endogenous peroxidase activity was blocked with 3% (v/v) H2O2 for 10 min. Tissues were incubated with Protein Block (DAKO) and then with monoclonal antibody S100A4 (1:500) for 4 h at room temperature or with α-SMA antibody (1:50) overnight. The slides with tissue sections were incubated with the polymer (Envision, DAKO) for 30 min. The reaction was stained with diaminobenzidine followed by hematoxylin counterstaining. The presence of FSP-1 and α-SMA in renal tissue was quantified as a percentage in the cortex using software for image analysis (NIS, Elements Advanced Research).
Cytometric Bead Array
Cytometric bead array for mouse cytokines (BD Biosciences) was performed to quantify IL-6 and tumor necrosis factor (TNF)-α in serum and kidney extracts, as described by the manufacturer.
Results are expressed as mean ± standard deviation. One-way analysis of variance (ANOVA) and Tukey posttest were performed to compare groups using GraphPad Prism 5.0 (GraphPad Software). Reverse transcriptase PCR results are presented as a ratio of the calibrator gene HPRT and presented in arbitrary units. Differences were considered statistically significant when p was <0.05.
All supplementary materials are available online at https://doi.org/www.molmed.org .
Adenine-Fed Jα18KO Mice Presented Higher Expression of KIM-1, TNF-α and Type I Collagen
To further investigate a role for iNKT cells in our renal injury model, we decided to activate them before tissue injury. This step could be relevant since other immune cells are involved in the process, and those cells could be masking the effect of iNKT cells deficiency.
Administration of α GalCer Reduced Creatinine Levels and Adenine-Induced Expression of IL-6 and TNF-α in WT Mice at d 10
WT mice were injected once with 5 µg αGalCer (iNKT cells potent agonist) intraperitoneally on the same day they started receiving adenine diet (d 0). Animals were euthanized at d 4 and 10.
αGalCer Challenge Reduced Renal Fibrosis and FSP-1 and α-SMA Staining in Renal Tissue
αGalCer Challenge Did Not Ameliorate Adenine-Induced Renal Injury in IFN-γKO Mice
It is still unclear how αGalCer attenuates the development of renal fibrosis. However, among NKT cell-produced cytokines, IFN-γ is known to have antifibrotic effects in experimental models, including the bleomycin-induced pulmonary fibrosis model (28,29). Yet, as shown above, we observed an increase in IFN-γ and STAT-1 (which is activated by IFN-γ and activates IFN-stimulated genes) gene expression after αGalCer administration.
To gain insight into the mechanism of protection conferred by αGalCer, we analyzed the role of IFN-γ in adenine-induced renal injury after αGalCer administration. Therefore, we submitted IFN-γKO mice to adenine feeding and also to αGalCer challenge.
The inflammatory process in kidney diseases is quite varied and involves the participation of cells, cytokines, chemokines and other factors. Several cell types participate in this process, with the contribution of T lymphocytes, neutrophils and macrophages. However, the role of NKT cells in renal diseases is still unclear. Our study demonstrated that αGalCer administration might improve renal function and injury in a model of adenine-induced tubule-interstitial nephritis.
The absence of NKT cells in KO mice had no significant influence on creatinine measurement, but led to a significant increase in gene expression of KIM-1, indicating that a deficiency in these cells may be detrimental to the kidney in this model. Another protein related to kidney injury is NGAL, and it was also increased after adenine feeding. These two tubular proteins might reflect a direct aggression of adenine crystals to renal tubules.
Since TNF-α is a proinflammatory cytokine and it is related to interstitial fibrosis, we also analyzed it. In our results, we observed a significant increase in gene expression of TNF-α and TGF-β in Ja18KO mice, indicating that the absence of invariant NKT cells may aggravate the inflammatory process and consequently the renal interstitial fibrosis. Quantifying tubule-interstitial fibrosis and mRNA expression of type I collagen could best assess the involvement of these proinflammatory and profibrotic cytokines. mRNA expression of type I collagen was significantly increased in adenine-fed Jα18KO mice when compared with adenine-fed WT mice, which could indicate increased fibrosis. Renal fibrosis was increased in both WT and Jα18KO mice submitted to adenine feeding, but there was no difference between these two groups. Hence, we evaluated other histological changes besides fibrosis, and we analyzed tubular degeneration, tubular necrosis, inflammatory infiltrate and tubular hypertrophy. In two of these parameters, adenine-fed Jα18KO mice had higher scores, which could corroborate the other results suggesting that these KO mice present worse renal injury.
Because the inflammatory process in kidney diseases is complex and involves other immune cells, the absence of iNKT cells by themselves may not be the best method to assess their role. Thus, we also tested another technique to see how activated iNKT cells could participate in the injury process. To activate iNKT cells, we administered a known agonist of these cells, the glycolipid αGalCer. αGalCer is presented by antigen-presenting cells through the molecule CD1d. This complex binds to the TCR of NKT cells with high affinity, and such attachment activates iNKT cells (30,31). In our experiments, we observed that the administration of αGalCer could improve renal function in our model, since there was a decrease in serum creatinine levels, IL-6 gene expression, serum TNF-α and renal fibrosis. Although NGAL levels were not reduced after αGalCer administration, this might imply that the tubular injury still exists because of the physical presence of crystals, but the inflammatory process could be minimized. A later time point analysis should be addressed in future studies to confirm this idea.
Renal interstitial fibrosis is characterized by tubular atrophy, leukocyte infiltration, excessive deposition of extracellular matrix and accumulation of fibroblasts (24). Although other cells may be involved, the fibroblasts can be considered as key mediators of renal fibrosis (25,26), especially through the process of epithelial-mesenchymal transition. In this process, epithelial renal cells undergo transition to a fibroblast phenotype and contribute to the production of extracellular matrix components (4).
Given the important role of fibroblasts, we also analyzed in our study the FSP-1 expression in renal tissue. We observed that the administration of αGalCer in adenine-fed animals caused a significant reduction of FSP-1 and α-SMA compared with adenine-fed WT mice without αGalCer. Labeling of α-SMA is related to the contractile function acquired by the myofibroblasts during the fibrotic process. The acquisition of the myofibroblast phenotype may represent the response of the kidney fibroblasts to a stress that was recently proposed to be due to intratubular hydrodynamic forces and tubular stretch (for example, by obstruction, or in the case of our study, due to the deposition of adenine crystals within the tubules) (32).
The involvement of NKT cells in the process of fibrogenesis has been demonstrated in several studies with experimental models of liver, lung and kidney diseases. However, the role of NKT cells in some of these models is still controversial. In experimental models of liver diseases, Park et al. (33) demonstrated that carbon tetrachloride-induced liver injury led to increased hepatic fibrosis in Jα18KO mice. In experimental models of lung diseases, Kimura et al. (34) observed that the administration of αGalCer increased survival and reduced pulmonary fibrosis and TGF-β levels in the bleomycin model. In renal diseases, Pereira et al. (35) found that GSL-1 (another NKT agonist) modulates the development of experimental focal and segmental glomerulosclerosis (EFSG) and, in the study by Mesnard et al. (36), Jα18KO mice demonstrated worse renal function in anti-glomerular basement membrane (anti-GBM) glomerulonephritis. These data support our findings that Jα18 knockout mice are prone to a higher percentage of fibrosis and that administration of αGalCer was effective in reducing this process.
The study by Kimura et al. (34) also highlights an increase in IFN-γ levels after αGalCer treatment with a protective role in the bleomycin model. IFN-γ is the type II interferon synthesized by CD4+ Th1 and CD8+ lymphocytes, NK, B and NKT cells (37, 38, 39, 40, 41); it is considered to be a key player in Th1 immune responses with immunomodulatory effects on several immune cells (42), stimulating tumor cell cytotoxicity and antimicrobial activity and downregulating TGF-β and type I and II procollagens gene expression in lung fibrosis models (28,43). In renal diseases models, Kimura et al. (44) reported a protective role of IFN-γ in cisplatin-induced renal injury. In this case, IFN-γ can accelerate autophagic flux and therefore increase the viability of renal tubular cells. In our study, we observed increased mRNA expression of IFN-γ and STAT-1 at d 4 in mice receiving αGalCer and adenine diet. We also used IFN-γKO mice to observe its contribution in the adenine-induced renal injury model. The excessive ingestion of adenine in IFN-γKO mice also caused renal injury, but it was not improved after αGalCer administration, as we observed in WT mice. Our findings may indicate that the release of IFN-γ is one of the main factors contributing to the improvement in renal function after αGalCer administration. The pathways by which IFN-γ mediates the improvement observed in our study must be analyzed in further studies.
Taken together, previous studies and ours show that NKT cells may have different functions depending on the organ and/or the stimuli of the microenvironment in which they are set. However, their participation in the process of fibrogenesis and the mechanisms involved in it are not fully understood, which demonstrates the contribution of our work in attempting to elucidate the plasticity of these cells and their mechanisms of action in diseases.
The authors declare that they have no competing interests as defined by Molecular Medicine, or other interests that might be perceived to influence the results and discussion reported in this paper.
The authors thank Masaru Taniguchi at the RIKEN Research Center for Allergy and Immunology (Japan) for Jα18KO mice and Paulo Albe for preparing the histology slides. This work was supported by Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES), Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP grant numbers 07/07139-3, 2012/02270-2 and 2012/16794-3) and Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq, Complex Fluids INCT). The funders had no role in study design, data collection and analysis; decision to publish; or preparation of the manuscript.
Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, and provide a link to the Creative Commons license. You do not have permission under this license to share adapted material derived from this article or parts of it.
The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder.
To view a copy of this license, visit (https://doi.org/creativecommons.org/licenses/by-nc-nd/4.0/)