Abstract
Immune-mediated glomerular diseases like crescentic glomerulonephritis (cGN) are driven by inappropriately regulated cellular and humoral immune responses subsequently leading to renal tissue injury. Recent studies demonstrated the crucial role for regulatory T cells (Tregs) in suppressing pathogenic T-cell responses during nephrotoxic nephritis (NTN), a murine model of cGN. However, mechanisms of immune regulation in cGN are less clear. Here, we aim at investigating the role of the co-inhibitory PD-1/PD-L1 pathway in Treg-mediated suppression of renal inflammation. We demonstrated that Foxp3+ Tregs expressing PD-L1 infiltrate the kidney during NTN. Inhibition of PD-L1 signalling by using PD-L1−/− mice or by blockage of PD-L1 in wildtype mice resulted in an increased Treg frequency in the inflamed kidney. However, mice lacking PD-L1 developed more severe NTN associated with an elevated pathogenic renal Th1 immune response, which was reversed by blockage of IFNγ in these mice. Interestingly, lack of PD-L1 altered the gene expression profile of Tregs in homeostasis and kidney inflammation. Functionally, Tregs from nephritic PD-L1−/− mice had impaired suppressive capacity in vitro and failed to protect from NTN in vivo. Thus, PD-L1 displays a protective role in NTN, which is related to Treg-mediated suppression of the Th1 immune response.
Introduction
Crescentic glomerulonephritis (cGN) is a severe glomerular disease characterized by formation of glomerular crescents in Bowman’s space and a rapid loss of renal function. Inappropriately regulated cellular and humoral immune responses, which may result from defects in central and peripheral tolerance, drive cGN. Negative co-stimulatory pathways are crucial for the maintenance of peripheral tolerance by inducing inhibitory signals in lymphocytes. One negative co-stimulator receptor expressed on activated T cells and B cells is programed cell death-1 (PD-1) that is bound by programed cell death ligand-1 (PD-L1) and PD-L2. PD-L1 is expressed by hematopoietic and non-hematopoietic cells and can be further induced during inflammation. In contrast, PD-L2 expression is mostly restricted to activated dendritic cells (DCs) and macrophages1,2. The PD-l/PD-L1 pathway exerts important functions in immune regulation and promotes development and function of regulatory T cells (Tregs) by induction and maintenance of the Treg-specific transcription factor forkhead box protein P3 (Foxp3)3. Binding of PD-L1 to PD-1 during primary T-cell activation induces blockage of T-cell proliferation and cytokine production and inhibits cytotoxic activity and cell survival4,5. Moreover, effector T-cell reactivation and function is also negatively regulated by the PD-1/PD-L1 interaction6,7.
The PD-1/PD-L1 pathway has been implicated in immune regulation of kidney diseases. A single nucleotide polymorphisms in the PD-1 gene was associated with increased susceptibility of patients to systemic lupus erythematosus8. Moreover, aged PD-1−/− mice were shown to develop lupus-like glomerulonephritis9. Renal expression of PD-L1 was demonstrated in patients with lupus nephritis, tubulointerstitial nephritis or renal cell carcinoma10. Furthermore, several studies revealed that blockage of PD-1/PD-L1 interaction aggravated murine accelerated nephrotoxic serum nephritis11, ischemia reperfusion-induced kidney injury12, adriamycin nephropathy13 or lupus-like nephritis14. However, mechanisms by which the PD-1/PD-L1 pathway mediates immunosuppression during kidney disease are less clear.
Kidney-infiltrating Th1 and Th17 cells were found to drive renal inflammation in murine models of cGN by production of the pro-inflammatory cytokines interferon-γ (IFNγ) and IL-17, respectively15–19. CD4+ Foxp3+ Tregs are crucial for the control of such pro-inflammatory immune responses to prevent excessive tissue damage and autoimmunity. We have shown recently that Tregs contribute to immune regulation in nephrotoxic nephritis (NTN), the murine model of cGN, by inhibiting the pro-inflammatory Th1 immune response thereby ameliorating disease pathogenesis20. The suppressive effect of Tregs during NTN was partially attributed to expression of the anti-inflammatory cytokine IL-1021. In the present study, we investigated the immunoregulatory role of the co-inhibitory PD-1/PD-L1 pathway in Treg-mediated protection from renal injury.
Results
Lack of PD-L1 resulted in an enhanced recruitment of Tregs into the inflamed kidney
The coinhibitory PD-1/PD-L1 pathway was found to contribute to Treg-mediated control of inflammatory immune responses. In this context, it was shown that PD-L1−/− mice develop aggravated NTN and that lack of PD-L1 expression by cells of hematopoietic origin worsened disease pathogenesis11. Based on these finding, we asked whether Tregs might be responsible for PD-L1-mediated protection in NTN. Therefore, we induced NTN by injection of the nephritogenic NTN serum in FIR-tiger mice, which allow distinct detection of the Treg-specific transcription factor Foxp3 via flow cytometry22, and did Treg analysis in the T cell-mediated autologous phase 8 days after NTN induction. We analyzed glomerular damage by quantification of crescent formation in periodic acid-Schiff (PAS)-stained kidney sections20 and determination of proteinuria in urine by measurement of the albumin-creatinine-ratio. NTN serum-treated FIR-tiger mice developed severe NTN characterized by a high percentage of crescent formation and proteinuria whereas in naive FIR-tiger mice neither crescents nor proteinuria were detectable (Figs 1A,B). We showed an increased frequency of Foxp3+ Tregs in the inflamed kidneys of nephritic FIR-tiger mice compared to naive FIR-tiger mice (Fig. 1C, Supplemental Fig. 1A). Interestingly, the frequencies of renal Tregs expressing PD-L1 or its receptor PD-1 were strongly elevated in nephritic FIR-tiger mice (Fig. 1D) suggesting a function for the PD-1/PD-L1 pathway in Treg-mediated immune regulation in NTN.
To investigate the Treg response in absence of PD-1/PD-L1 signalling, we used PD-L1−/− mice. As PD-L1 is involved in T-cell development and Treg induction3,23, we analyzed the Treg compartment in primary and secondary lymphoid organs of naive PD-L1−/− mice. We excluded impaired generation of thymus-derived Foxp3+ Tregs since the frequencies of Helios+ and neuropilin-1+ Foxp3+ Tregs were comparable in PD-L1−/− and C57BL/6 wildtype (WT) mice. Moreover, we found no substantial difference in the frequencies of CD44lo CD62L+ central Tregs or CD44hi CD62L− effector Tregs (Fig. 1E, Supplemental Fig. 1B) indicating that lack of PD-1/PD-L1 signalling did not compromise the Treg compartment in naive PD-L1−/− mice.
FIR-tiger mice were crossed with PD-L1−/− mice to determine the renal Treg response during NTN in the absence of PD-L1 (Supplemental Figs 2, 3). We compared disease pathogenesis of NTN in FIR-tiger-PD-L1−/− mice with the already known disease course in nephritic PD-L1−/−. In line with previous findings11 and our own data concerning PD-L1−/− mice (Supplemental Fig. 4A,B), we demonstrated increased crescent formation and proteinuria in nephritic FIR-tiger-PD-L1−/− mice compared to nephritic FIR-tiger mice (Fig. 1F,G). Further, the humoral immune response was analyzed by determination of the IgG antibody response against the nephritogenic antigen. In nephritic FIR-tiger-PD-L1−/− mice, serum levels of mouse anti-sheep total IgG and of the isotypes IgG1, IgG2a/c, and IgG2b were enhanced compared to nephritic FIR-tiger mice (Fig. 1H). An elevated IgG antibody response was also determined in nephritic PD-L1−/− mice (Supplemental Fig. 4C). Thus, lack of PD-L1 aggravated disease pathogenesis of NTN in both FIR-tiger-PD-L1−/− mice and PD-L1−/− mice.
We analyzed renal mRNA expression of PD-1 and its two ligands PD-L1 and PD-L2 during NTN. Nephritic FIR-tiger mice expressed PD-L1 (Cd274) mRNA, which was absent in FIR-tiger-PD-L1−/− mice. We showed mRNA expression of PD-L2 (Pdcd1lg2) during NTN that was not altered in mice lacking PD-L1. In contrast, renal PD-1 (Pdcd1) mRNA expression was up-regulated in nephritic FIR-tiger-PD-L1−/− mice compared to nephritic FIR-tiger mice (Fig. 1I). The same findings were shown in nephritic PD-L1−/− mice. Moreover, PD-1 mRNA expression was even elevated in naive PD-L1−/− mice compared to naive WT mice and was further enhanced during NTN (Supplemental Fig. 4D). Interestingly, we detected an increased frequency of Foxp3+ Tregs in the inflamed kidneys of FIR-tiger-PD-L1−/− mice compared to nephritic FIR-tiger mice. The renal Treg population in nephritic FIR-tiger-PD-L1−/− mice did not express PD-L1 and showed increased expression of PD-1 (Fig. 1J). Thus, recruitment of Foxp3+ Tregs into the inflamed kidney was increased in the absence of PD-L1.
Up-regulated renal Th1 immune response in the absence of PD-L1
It has been shown that kidney-infiltrating Th1 cells and Th17 cells drive disease pathogenesis of NTN in WT mice15–19. Since Tregs were found to suppress Th1 cells during NTN20, we investigated the CD4+ T cell-mediated immune response in the absence of PD-1/PD-L1 signalling by using nephritic PD-L1−/− mice. We analyzed renal mRNA expression and demonstrated elevated gene expression levels of the Th1-associated cytokines IFNγ (Ifng) and IL-12p40 (Il12b), and of the transcription factor T-bet (Tbx21) compared to nephritic WT mice. This correlated with enhanced expression of the IFNγ-inducible, Th1 cell-recruiting chemokine CXCL10 (Cxcl10) in nephritic PD-L1−/− mice. In contrast, mRNA expression of genes associated with a Th17 cell-mediated immune response such as IL-6 (Il6) and RORγt (Rorc) was down-regulated (Fig. 2A). In homeostasis, renal gene expression of IFNγ, IL-12p40, T-bet, CXCL10, and IL-6 was not altered in naive PD-L1−/− mice compared to WT mice whereas IL-17A and RORγt expression was not detectable (Supplemental Fig. 5A). We further investigated the local pro-inflammatory immune response by intracellular cytokine staining in renal T-cell populations. The frequency of CD4+ T cells was increased in the inflamed kidneys of nephritic PD-L1−/− mice (Fig. 2B). In line with the gene expression data, we detected a significantly higher frequency of renal IFNγ-expressing Th1 cells in nephritic PD-L1−/− mice than nephritic WT mice whereas the frequency of IL-17A-expressing Th17 cells was reduced. (Fig. 2C). We further showed that the frequency of Th1 cells did not differ in naive PD-L1−/− mice and WT mice whereas Th17 cells were not detectable (Supplemental Fig. 5B).
We reinforced the findings in PD-L1−/− mice by blockage of PD-L1 in WT mice. Therefore, WT mice were treated with an anti-PD-L1 antibody daily starting one day after induction of NTN. We showed that crescent formation, proteinuria, and humoral immune response were increased in anti-PD-L1 antibody-treated nephritic WT mice compared to isotype-treated nephritic WT mice (Fig. 2D–F). Renal mRNA expression of the Th1-associated molecules IFNγ, T-bet, IL-12p40, and CXCL10 was elevated after blockage of PD-L1 in WT mice. Interestingly, mRNA expression of Foxp3 was also increased (Fig. 2G) and this correlated with an enhanced frequency of renal Foxp3+ Tregs in anti-PD-L1 antibody treated nephritic WT mice compared to isotype-treated nephritic WT mice (Fig. 2H). We further detected an elevated frequency of CD4+ T cells and IFNγ+ Th1 cells in the kidneys of antibody-treated nephritic WT mice (Fig. 2I,J). Taken together, lack of PD-L1 resulted in an elevated renal Th1 immune response and aggravated NTN despite an increased frequency of Foxp3+ Tregs in the inflamed kidney.
Augmented systemic Th1 immune response in the absence of PD-L1
To investigate the role of PD-L1 regarding the systemic immune response during NTN, the phenotype of splenic CD4+ T cells was analyzed in nephritic PD-L1−/− and WT mice. We found no alterations in the frequency of CD4+ T cells in nephritic PD-L1−/− mice (Fig. 3A). However, we demonstrated an enhanced frequency of splenic IFNγ+ Th1 cells in the absence of PD-L1. In contrast, IL-17A was not substantially expressed by splenic CD4+ T cells during NTN (Fig. 3B). We further detected elevated IFNγ levels in culture supernatants of sheep IgG-stimulated splenocytes from nephritic PD-L1−/− mice (Fig. 3C). We also analyzed splenic antigen-presenting cell populations that drive T-cell activation. No differences were detected in the frequencies of CD11b+ Ly6C+ monocytes/macrophages, F4/80+ CD11b+ macrophages or CD11c+ CD11b+ DCs in nephritic PD-L1−/− and WT mice (Fig. 3D). Interestingly, the frequency of DCs expressing MHCII and their overall MHCII expression was increased in nephritic PD-L1−/− mice (Fig. 3E).
Ameliorated NTN after blockage of IFNγ in PD-L1−/− mice
Having shown that PD-L1 deficiency resulted in an increased IFNγ response and more severe kidney damage during NTN, we asked whether elevated IFNγ levels drive disease pathogenesis of nephritic PD-L1−/− mice. Therefore, we blocked IFNγ by injection of a neutralizing anti-IFNγ antibody one day before and four days after induction of NTN in PD-L1−/− mice and analyzed disease pathology. We demonstrated reduced crescent formation and proteinuria in anti-IFNγ antibody-treated nephritic PD-L1−/− mice compared to isotype-treated nephritic PD-L1−/− mice. Interestingly, disease severity of anti-IFNγ antibody-treated nephritic PD-L1−/− mice was diminished to levels of isotype-treated nephritic WT mice (Fig. 4A,B). Renal mRNA expression analysis revealed strongly decreased expression of genes associated with a Th1 immune response such as IFNγ, T-bet, IL-12p40, and CXCL10 after neutralization of IFNγ in nephritic PD-L1−/− mice. Moreover, Foxp3 mRNA expression was also decreased (Fig. 4C). In addition, the frequencies of renal CD4+ T cells and IFNγ+ Th1 cells were reduced in anti-IFNγ antibody-treated nephritic PD-L1−/− mice (Fig. 4D,E). Taken together, blockage of IFNγ led to reduced renal infiltration of Th1 cells and ameliorated NTN in PD-L1−/− mice.
Altered gene expression profile of Tregs in the absence of PD-L1
Having shown that PD-L1 deficiency did not result in impaired Treg differentiation or renal recruitment, we asked whether lack of PD-L1 instead compromises Treg function. To characterize more specifically the phenotype of Tregs in absence or presence of PD-L1 under homeostatic and inflammatory conditions, we FACS-sorted Tregs from naive and nephritic FIR-tiger-PD-L1−/− and FIR-tiger mice and subjected these cells to a quantitative gene expression array profiling immunology-related genes (Fig. 5A). Interestingly, the gene expression pattern of Tregs from FIR-tiger-PD-L1−/− mice was distinct from that of Tregs from FIR-tiger mice even in the steady state. They showed up-regulated expression of genes associated with cytokine/chemokine signaling, cell adhesion/migration and Treg function. To a lesser extent, we also found genes that were down-regulated in Tregs from FIR-tiger-PD-L1−/− mice. Kidney inflammation altered gene expression of Tregs from nephritic FIR-tiger-PD-L1−/− and FIR-tiger mice but again, there were strong differences in the gene expression profile of both Treg populations (Fig. 5B, Supplemental Fig. 6A,B). For instance, in contrast to Tregs from FIR-tiger mice, Tregs from FIR-tiger-PD-L1−/− mice did not increase IL-10 expression during NTN. Interestingly, Tregs from naive and nephritic FIR-tiger-PD-L1−/− mice showed up-regulated expression of IFNγ compared to Tregs from naive and nephritic FIR-tiger mice. We also found strongly elevated expression of PD-1 in the absence of PD-L1. Moreover, Tregs from nephritic FIR-tiger mice maintained high expression of the high-affinity IL-2Ra chain (Il2ra) during renal inflammation whereas Tregs from nephritic FIR-tiger-PD-L1−/− mice showed decreased expression. We demonstrated increased expression of molecules associated with Treg function such as CD39 (Entpd1) and T-cell immunoreceptor with Ig and ITIM domains (Tigit) in the absence of PD-L1. In contrast, only Tregs from FIR-tiger mice showed enhanced expression of granzyme B (GzmB) during NTN. Lack of PD-L1 resulted in up-regulated expression of the chemokines CXCL10, CCL5, and XCL1, of the cytokine colony stimulating factor 1 (CSF1), and of the chemokine receptor CXCR3 (Fig. 5C). Thus, lack of PD-L1 profoundly altered the gene expression profile of Tregs in homeostasis and kidney inflammation.
Impaired immunosuppressive capacity of Tregs in the absence of PD-L1
To analyze Treg function in vitro, we performed suppression assays. Tregs were isolated from nephritic PD-L1−/− and WT mice and co-cultured with eFlour670-labeld CD4+ CD25− responder T cells from CD45.1 mice in the presence of anti-CD3 antibody for 3 days. Tregs from nephritic WT mice strongly reduced proliferation and activation of responder CD4+ T cells. In contrast, Tregs from nephritic PD-L1−/− mice failed to suppress responder CD4+ T-cell proliferation and activation (Fig. 6A). By performing adoptive cell transfer experiments, we analyzed the suppressive capacity of Tregs in vivo. FACS-sorted CD4+ CD25− T cells were i.v. injected either alone or together with Tregs from nephritic PD-L1−/− or WT mice into Rag1−/− mice. Two days later, NTN was induced. Tregs from nephritic WT mice did not significantly alter crescent formation (Fig. 6B) but improved kidney function demonstrated by reduced proteinuria (Fig. 6C). Beside glomerular damage, tubulointerstitial damage also contributes to impairment of renal function in kidney disease and we showed that Tregs from nephritic WT mice ameliorated tubulointerstitial injury during NTN (Fig. 6D). In contrast, Tregs from nephritic PD-L1−/− mice had no suppressive effect on disease pathogenesis of NTN (Fig. 6B–D) indicating impaired immunosuppressive function of Tregs in the absence of PD-L1.
Discussion
Crescentic glomerulonephritis is a life-threatening disease triggered by so far poorly defined mechanisms. Thus, identifying molecular and cellular pathways involved in the pathogenesis of cGN is of high clinical relevance. In this study, we showed that the co-inhibitory PD-1/PD-L1 pathway contributes to immune regulation in cGN by promoting Treg-mediated suppression of the inflammatory Th1 immune response.
During inflammation, lymphocyte activation has to be regulated in order to dampen ongoing immune responses and to prevent autoimmunity. The crucial immunoregulatory function of Tregs in kidney disease was demonstrated in various studies and are reviewed elsewhere24. We found that the frequency of Tregs expressing PD-L1 was increased during NTN. There is some evidence in the literature that Tregs mediate immunosuppression by PD-L1-driven lymphocyte inhibition. Blockage of the PD-1/PD-L1 pathway by using an anti-PD-L1 antibody was shown to inhibit Treg-mediated suppression of T-cell activation in vitro25,26. Moreover, antigen-specific suppression of autoreactive B cells by PD-L1-expressing Tregs was demonstrated in a mouse model with glomerular model antigen expression27. In our study, we showed an elevated renal Th1 immune response as well as IgG antibody response in nephritic PD-L1−/− mice possibly due to lack of PD-L1 expression by Tregs.
In contrast to a previous study, which linked PD-1/PD-L1 signaling to Treg induction3, we found that lack of PD-L1 did not affect development of Foxp3+ Tregs. The number of Tregs was even increased in the inflamed kidneys of FIR-tiger-PD-L1−/− mice. The ability of Tregs to access inflammatory tissue is regulated by expression of receptors for chemokines produced in the inflamed organ28. We showed elevated gene expression of the chemokine receptor CXCR3 by Tregs from nephritic FIR-tiger-PD-L1−/− mice and together with enhanced renal expression of the corresponding CXCR3 ligand CXCL10, this might account for increased recruitment of Tregs in the absence of PD-L1. This assumption is supported by a study showing that Treg-specific deletion of CXCR3 resulted in reduced renal infiltration of Tregs during NTN and an exaggerated Th1 immune response29. However, despite elevated Treg numbers in the inflamed kidney, lack of PD-L1 aggravated disease pathogenesis of NTN and was associated with an amplified renal Th1 immune response. Since we have shown previously that Tregs control the Th1 immune response during NTN20, these findings suggest an impaired immunosuppressive function of Tregs in the absence of PD-L1. Indeed, we showed that Tregs from nephritic PD-L1−/− mice failed to inhibit CD4+ T-cell activation or to suppress disease pathology of NTN. One mechanism by which Tregs mediate immunosuppression during NTN is by production of the anti-inflammatory cytokine IL-1021. Gene expression analysis revealed that in the absence of PD-L1, Tregs did not up-regulate expression of IL-10 during kidney inflammation. Moreover, they down-regulated gene expression of the high affinity IL-2Ra chain. Since IL-2/IL-2R signaling has been shown to be essential for Treg function and fitness30, this might affect immunosuppressive capacity of Tregs during NTN. It has been further shown that PD-1-deficient Tregs exhibit a more suppressive phenotype than PD-1+ Tregs31. Moreover, PD-1 expression by Tregs of viral hepatitis patients inhibited their immunosuppressive function32. Since Tregs from nephritic PD-L1−/− mice up-regulated expression of PD-1, this might be another reason for their impaired immunosuppressive capacity. Tregs also promote immunosuppression by inducing PD-L1 expression on DCs, which in turn suppress T-cell activation as demonstrated in graft-versus-host disease33. In the absence of PD-L1, DCs do not acquire the ability to promote tolerance by this mechanism. We even found that DCs from nephritic PD-L1−/− mice exhibit a more activated phenotype with elevated MHCII expression that could drive T-cell activation and polarization during NTN.
Increased frequencies of Th1 cells in the kidneys of nephritic PD-L1−/− mice might also be caused by elevated renal expression of the Th1 cell-attracting chemokine CXCL10 whose expression is further triggered by IFNγ. This assumption was supported by the finding that inhibition of IFNγ in nephritic PD-L1−/− mice reduced CXCL10 expression and renal recruitment of Th1 cells. Since blockage of IFNγ also ameliorated NTN, we conclude that elevated IFNγ levels in the absence of PD-L1 drive disease pathogenesis. Enhanced IFNγ-mediated immune responses were shown in other diseases caused by a nonfunctional PD-1/PD-L1 pathway. For example, increased disease severity of EAE in PD-1−/− mice was linked to a higher frequency of IFNγ-expressing T cells34. In graft-versus-host disease, rapid mortality of PD-L1−/− mice was associated with elevated Th1 cytokine production35, and in heart transplantation, absence of PD-L1 promoted Th1-cell polarization and allograft rejection36 strongly indicating the essential role of the PD-1/PD-L1 pathway in controlling Th1 immune responses in autoimmune diseases.
The immunosuppressive function of the PD-1/PD-L1 pathway was demonstrated in several autoimmune diseases. PD-1−/− mice developed lupus-like glomerulonephritis, destructive arthritis, and dilated cardiomyopathy9,37. Blockage of PD-1/PD-L1 interaction aggravated diabetes in nonobese diabetic mice7,38, accelerated experimental autoimmune encephalomyelitis (EAE)34, and worsened disease pathogenesis of accelerated NTN11. We confirmed the pathological findings of the study by Menke et al. by using FIR-tiger-PD-L1−/− and PD-L1−/− mice and by blockage of PD-L1 in WT mice. The authors also showed that PD-L2−/− mice developed more severe accelerated NTN indicating an immunoregulatory function for the second PD-1 ligand in kidney inflammation11. However, renal expression of PD-L2 was not altered in nephritic FIR-tiger-PD-L1−/− and PD-L1−/− mice and despite up-regulated expression of PD-1, PD-L2 did not compensate the absence of PD-L1.
Several therapeutic strategies activating the PD-1/PD-L1 pathway in autoimmune disease have been tested in mice. One study reported that overexpression of PD-L1 on DCs reduced severity of EAE39. Systemic activation of the PD-1/PD-L1 pathway by injection of a PD-L1/Fc fusion protein ameliorated progression of intracerebral hemorrhage40, colitis41, and collagen-induced arthritis42. In kidney disease, administration of a recombinant adenovirus encoding PD-L1 attenuated lupus-like nephritis43, and treatment with a PD-L1/Fc fusion protein ameliorated experimental autoimmune glomerulonephritis in rats44. In contrast, inhibition of the PD-1/PD-L1 pathway by administration of the checkpoint inhibitors pembrolizumab or nivolumab during cancer immunotherapy caused a higher incidence of acute interstitial nephritis in patients with melanoma or lung cancer45. The results of our study illustrate the important immunoregulatory function of the PD-1/PD-L1 pathway in NTN by ensuring proper Treg function in renal inflammation. Therefore, stimulating this pathway may provide a therapeutic option in cGN.
Methods
Animals
C57BL/6, PD-L1−/−, Rag1−/−, CD45.1, FIR-tiger (Foxp3-IRES-mRFP [FIR] x IL-10-IRES-GFP [tiger])22, and FIR-tiger-PD-L1−/− mice were bred in the animal facility of the University Medical Center Hamburg-Eppendorf (Hamburg, Germany). A detailed genotyping protocol of FIR-tiger-PD-L1−/− mice and analysis of PD-L1 expression in these mice is shown in Supplemental Figs 2 and 3. FIR-tiger mice and PD-L1−/− mice were provided by Richard Flavell (Yale University, New Haven, CT) and Lieping Chen (Yale University, New Haven, CT), respectively. Mouse experiments were conducted according to the German animal protection law and approved by the institutional review board (Behörde für Gesundheit und Verbraucherschutz, Hamburg, Germany; G20/13). Mice received humane care according to the national guidelines of the National Institutes of Health in Germany.
Animal treatment and functional studies
NTN was induced in male mice (8–12 weeks old) by intraperitoneal (i.p.) injection of 2.5 mg nephrotoxic sheep serum per gram of mouse body weight as described previously46. Mice were sacrificed 8 days after NTN induction. To assess systemic antibody response, heart blood was drawn from individual mice. One day before killing, mice were housed in metabolic cages for urine collection. Albuminuria was determined by ELISA (Mice-Albumin Kit; Bethyl, Montgomery, TX). C57BL/6 mice were treated i.p. with an anti-PD-L1 antibody (250 µg/mouse; 10 F.9G2; BioXCell, West Lebanon, NH) daily starting one day after NTN induction. As isotype control, mice received rat IgG2b (250 µg/mouse; LTF-2; BioXCell). PD-L1−/− mice received i.p. an anti-IFNγ antibody (250 µg/mouse; XMG1.2; BioXCell) one day before and 4 days after NTN induction. As isotype control, rat IgG1 (1 mg/mouse; HRPN; BioXCell) was injected.
Histological analysis
Immunohistochemistry was performed by routine procedures as described previously47. Crescent formation was assessed in 30 glomeruli/mouse in a blinded fashion in PAS-stained, paraffin-embedded kidney sections.
Antigen-specific humoral immune response
Mouse anti-sheep IgG antibody titers were measured by ELISA using sera collected 8 days after NTN induction. In brief, ELISA microtiter plates were coated with 100 µl sheep IgG (100 µg/ml; Sigma-Aldrich, St. Louis, MO) in carbonate-bicarbonate buffer overnight at 4 °C. After blocking with 1% BSA in TBS, the plates were incubated with serial dilutions of mouse serum for one hour at room temperature. Bound mouse IgG was detected using peroxidase-conjugated goat anti-mouse IgG (Biozol, Eching, Germany), TMB peroxidase substrate (Thermo Fisher Scientific, Waltham, MA), and absorbance readings (at 450 nm). Lack of cross-reactivity of the secondary antibody with sheep IgG was demonstrated by omitting the primary antibody. Bound mouse immunoglobulin isotypes were detected using peroxidase-conjugated rabbit anti-mouse IgG (total), IgG1, IgG2a/c, and IgG2b antibodies (Zymed-Invitrogen, Karlsruhe, Germany).
Isolation of renal cells and splenocytes
Kidneys and spleens were harvested from nephritic mice 8 days after NTN induction. Splenic tissue was passed through 70 µm nylon meshes prior to erythrocyte lysis using NH4Cl. Kidneys were finely minced and digested for 40 min at 37 °C with 0.4 mg/ml collagenase D (Roche, Mannheim, Germany) and 0.01 mg/ml DNase I (Roche) in RPMI 1640 supplemented with 10% heat-inactivated fetal calf serum (Thermo Fisher Scientific). Erythrocytes were lysed with NH4Cl and cell suspensions were sequentially filtered through 70 µm and 40 µm nylon meshes and washed with Ca2+- and Mg2+-free HBSS (Thermo Fisher Scientific).
Flow cytometry
Renal cells and splenocytes were incubated with anti-CD16/32 antibody (93; BioLegend, San Diego, CA) prior to antibody staining to prevent unspecific binding. LIVE/DEAD Fixable Red Dead Cell Stain Kit (Thermo Fisher Scientific) was used to exclude dead cells. Cells were surfaced-stained with fluorochrome-labeled antibodies specific to CD3 (AF700; 17A2), PD-1 (FITC; J43), PD-L1 (PE; MIH5; all eBioscience, San Diego, CA), CD4 (BV711; 13B8.2), CD45.1 (A20; all BD Biosciences, San Jose, CA), CD45 (PerCP, BV570; 30-F11), CD11b (AF700; M1/70), CD11c (BV605; N418), Ly-6C (PerCP; HK1.4), MHCII (FITC; M5/114.15.2), TCRβ (PE-Cy7; H57-597), CD25 (PE; PC-61), Nrp-1 (PE; 3E12), Helios (FITC; 22F6), CD44 (BV421; IM7), CD62L (PerCP-Cy5.5; MEL-14; all BioLegend). For intracellular cytokine staining, cells were stimulated with phorbol myristate acetate (10 ng/ml) and ionomycin (250 ng/ml) for 5 h with the addition of brefeldin A (1 µg/ml; all Sigma Aldrich) after 30 min. After surface and Live/Dead staining, cells were fixed in Fix/Perm solution before incubation in Perm/Wash buffer (both BD Biosciences) with antibodies specific to IFNγ (APC; XMG1.2; eBioscience) and IL-17A (V450; TC11-18H10; BD Pharmingen). For intranuclear staining, cells were fixed using the Transcription Factor Staining Buffer Set (eBioscience) and incubated in Permeabilization buffer with an antibody specific to Foxp3 (AF647; MF-14; BioLegend). Flow cytometry data were analyzed by using fluorescence minus one controls.
Antigen-specific cellular immune response
Splenocytes were cultured at a density of 4 × 106 cell/ml in RPMI 1640 medium supplemented with 10% fetal bovine serum, 1% penicillin/streptomycin, 1% sodium pyruvate, and 0.1% β-mercaptoethanol (all Gibco/ThermoFisher Scientific) in the presence of 20 µg/ml sheep IgG for three days. Cytokine levels were determined in culture supernatants using 96-well high-binding flat-bottom microtiter plates (Greiner Bio-One, Frickenhausen, Germany) and Duo Set ELISA for IFNγ (BioLegend, San Diego, CA) according to the manufacturer’s protocol.
Suppression assay
Tregs were isolated from PD-L1−/− and WT mice 8 days after induction of NTN. Therefore, CD4+ T cells were enriched using the CD4+ T Cell Isolation Kit (Miltenyi Biotec, Bergisch Gladbach, Germany). Subsequently, CD4+ CD25hi Tregs were sorted by FACS (BD FACSAriaTM III sorter, BD Biosciences). CD4+ CD25− responder T cells from CD45.1 mice were isolated by FACS and labeled with Cell Proliferation Dye eFlour670. Then, 1 × 105 responder T cells were co-cultured with 1 × 105 Tregs in the presence of an anti-CD3 antibody (145-2C11; BioLegend) for 3 days.
Adoptive transfer experiments
CD4+ CD25hi Tregs were sorted by FACS from nephritic PD-L1−/− and WT mice. 1 × 106 FACS-sorted CD4+ CD25− T cells from CD45.1 mice were adoptively transferred into Rag1−/− mice either alone or in combination with 5 × 105 Tregs from nephritic PD-L1−/− or WT mice. After 2 days, NTN was induced and mice were analyzed 8 days later.
Quantitative real-time RT- PCR analysis
Total RNA was isolated from shock-frozen kidney tissue using the NucleoSpin RNA Kit (Machery-Nagel, Duren, Germany) according to the manufacturer’s instruction. RNA was transcribed into cDNA using the Verso cDNA Synthesis Kit (Life Technologies, Carlsbad, CA) on a MyCycler thermal cycler (BioRad, München, Germany). Quantitative RT-PCR was performed using the ABsolute qPCR SYBR Green Mix (Thermo Scientific). The relative mRNA levels were calculated using the ∆∆CT method after normalization to the reference genes β-actin or 18 S. Quantification was shown in x-fold changes to the corresponding control cDNA. Primers were obtained from Metabion (Martinsried, Germany). Sequences of the primers are listed in Supplemental Table 1.
Treg gene expression analysis
Foxp3+ Tregs were isolated from spleen and lymph nodes of naive and nephritic FIR-tiger and FIR-tiger-PD-L1−/− mice. Therefore, CD4+ T cells were enriched from single cell suspensions by using the CD4+ T Cell Isolation Kit (Miltenyi Biotec). Thereafter, CD4+ Foxp3+ (mRFP+) Tregs were purely isolated by FACS. RNA of 1–2 × 106 Tregs was isolated by the RNeasy Mini Kit (Quiagen) and digested with RNase-free DNase I (Quiagen) according to the manufacturer’s instructions. Gene expression analysis was performed using the NanoString assay with the nCounter Immunology Panel profiling 561 immunology-related genes (NanoString Technologies, Hamburg, Germany) according to the manufacturer’s instructions. The results were analyzed with the nSolver Analysis Software 2.5 (NanoString Technologies). Data were calculated in x-fold changes compared to the corresponding control mRNA and displayed as heat map using the web server Heatmapper48. Clustering was done using the average linkage and the Pearson distance.
Statistical analyses
Data were analyzed using the GraphPad Prism software (GraphPad software, San Diego, CA). Statistical comparison was carried out using the Mann-Whitney U test or the one-way ANOVA with post analysis by Tukey-Kramer test. Data were expressed as means ± SEM. A p value of less than 0.05 was considered statistically significant with the following ranges *p < 0.05, **p < 0.01, and ***p < 0.001.
Supplementary information
Acknowledgements
The authors acknowledge the excellent technical assistance of Elena Tasika and Carsten Rothkegel (Institute of Experimental Immunology and Hepatology, University Medical Center Hamburg-Eppendorf) and of Oliver Krenkel (Department of Medicine III, RWTH-University Hospital Aachen). We thank all members of the FACS Sorting Core Unit (University Medical Center Hamburg-Eppendorf) for cell sorting. We further thank Prof. Richard Flavell and Prof. Lieping Chen (both Yale University, New Haven, CT) for providing us FIR-tiger mice and PD-L1−/− mice, respectively. This work was supported by the Deutsche Forschungsgemeinschaft (DFG): SFB 1192 project A1 granted to UP and A2 granted to GT.
Author Contributions
K.N.: designed and performed experiments, wrote the manuscript; A.O.: designed and performed experiments, reviewed the manuscript; P.C.B.: acquired data; A.O.: acquired data; F.T.: performed NanoString analysis; H.-J.P.: acquired data, reviewed the manuscript; U.P.: obtained funding, reviewed the manuscript; G.T.: designed study concept, obtained funding, reviewed the manuscript
Data Availability
The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.
Competing Interests
The authors declare no competing interests.
Footnotes
Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Katrin Neumann and Annett Ostmann contributed equally.
Contributor Information
Katrin Neumann, Email: kat.neumann@uke.de.
Gisa Tiegs, Email: g.tiegs@uke.de.
Electronic supplementary material
Supplementary information accompanies this paper at 10.1038/s41598-018-38432-3.
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Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.