Kidney VISTA prevents IFN-γ/IL-9 axis–mediated tubulointerstitial fibrosis after acute glomerular injury

Severe glomerular injury ultimately leads to tubulointerstitial fibrosis that determines patient outcome, but the immunological molecules connecting these processes remain undetermined. The present study addressed whether V-domain Ig suppressor of T cell activation (VISTA), constitutively expressed in kidney macrophages, plays a protective role in tubulointerstitial fibrotic transformation after acute antibody-mediated glomerulonephritis. After acute glomerular injury using nephrotoxic serum, tubules in the VISTA-deficient (Vsir–/–) kidney suffered more damage than those in WT kidneys. When interstitial immune cells were examined, the contact frequency of macrophages with infiltrated T cells increased and the immunometabolic features of T cells changed to showing high oxidative phosphorylation and fatty acid metabolism and overproduction of IFN-γ. The Vsir–/– parenchymal tissue cells responded to this altered milieu of interstitial immune cells as more IL-9 was produced, which augmented tubulointerstitial fibrosis. Blocking antibodies against IFN-γ and IL-9 protected the above pathological process in VISTA-depleted conditions. In human samples with acute glomerular injury (e.g., antineutrophil cytoplasmic autoantibody vasculitis), high VISTA expression in tubulointerstitial immune cells was associated with low tubulointerstitial fibrosis and good prognosis. Therefore, VISTA is a sentinel protein expressed in kidney macrophages that prevents tubulointerstitial fibrosis via the IFN-γ/IL-9 axis after acute antibody-mediated glomerular injury.


Introduction
Glomerulonephritis is the most common form of glomerular injury, and if severe, it can lead to tubular dysfunction and leave irreversible fibrotic matrix in the interstitium (1,2). This pathological process is clinically evident such that heavy proteinuria is a risk factor for chronic kidney disease and end-stage kidney disease (3). Linkage of pathologies between glomerular and tubulointerstitial compartments may be explainable by the fact that filtered proteins in glomeruli have direct toxic effects on tubules if reabsorbed, and these tubules display altered gene signatures such as apoptosis and produce inflammatory cytokines (4). Disrupted glomerulotubular balance and tubuloglomerular feedback can augment the progression of injury, with several mediators, such as reactive oxygen species, chemokines, and cytokines, involved in this process (5,6). Infiltrated immune cells should play a direct role in the above linkage because these cells are found in the interstitial area surrounding glomeruli and tubules, particularly after severe glomerulonephritis. However, how immune cells participate in this linkage during inflammatory or antiinflammatory processes is not yet fully understood.
There are certain immune cell subsets that reside in nonlymphoid peripheral tissues (named tissue-resident immune cells) and may have a role in the maintenance of immunological homeostasis (7,8). In particular, tissue-resident macrophages and memory T cells have received attention as the first layer of protection against harmful microorganisms. In mouse kidneys, most resident immune cells are kidney-resident macrophages (9), and their residency in the tubulointerstitial area remains consistent during inflammation (10,11). Our previous work showed that this macrophage subset had both inflammatory and repair roles after tubular ischemia as a noninfectious injury and functioned by inhibiting overactivation of infiltrated T cells and scavenging dying cells (10). When membrane molecules relevant to this repair function were screened, V-domain Ig suppressor of T cell activation (VIS-TA) was identified; interestingly, it was highly and constitutively expressed in kidney-resident macrophages and less in kidneyinfiltrating macrophages. VISTA is well known to be induced after inflammatory insult or in the tumor environment (12)(13)(14)(15), but kidney-resident macrophages substantially express VISTA even under normal conditions without any insult. The present study hypothesized that this frontline molecule may play a protective role in the linkage between glomerular injury and subsequent tubulointerstitial fibrosis. When VISTA was depleted (Vsir -/-), tubules suffered more damage in the nephrotoxic nephritis (NTN) model, resulting in acute antibody-mediated glomerular injury. In NTN-induced Vsir -/mice, the contact frequency of macrophages with infiltrated T cells increased and the immunometabolic characteristics of T cells changed, resulting in high oxidative phosphorylation and fatty acid metabolism and overproduction of IFN-γ. Parenchymal IL-9 levels were increased in response to the above immunological actions in the interstitium and generated the fibrotic footprint and consequently kidney dysfunction. Human cases of antineutrophil Severe glomerular injury ultimately leads to tubulointerstitial fibrosis that determines patient outcome, but the immunological molecules connecting these processes remain undetermined. The present study addressed whether V-domain Ig suppressor of T cell activation (VISTA), constitutively expressed in kidney macrophages, plays a protective role in tubulointerstitial fibrotic transformation after acute antibody-mediated glomerulonephritis. After acute glomerular injury using nephrotoxic serum, tubules in the VISTA-deficient (Vsir -/-) kidney suffered more damage than those in WT kidneys. When interstitial immune cells were examined, the contact frequency of macrophages with infiltrated T cells increased and the immunometabolic features of T cells changed to showing high oxidative phosphorylation and fatty acid metabolism and overproduction of IFN-γ. The Vsir -/parenchymal tissue cells responded to this altered milieu of interstitial immune cells as more IL-9 was produced, which augmented tubulointerstitial fibrosis. Blocking antibodies against IFN-γ and IL-9 protected the above pathological process in VISTA-depleted conditions. In human samples with acute glomerular injury (e.g., antineutrophil cytoplasmic autoantibody vasculitis), high VISTA expression in tubulointerstitial immune cells was associated with low tubulointerstitial fibrosis and good prognosis. Therefore, VISTA is a sentinel protein expressed in kidney macrophages that prevents tubulointerstitial fibrosis via the IFN-γ/IL-9 axis after acute antibody-mediated glomerular injury.
subsets were evaluated, VISTA expression was increased in CD4 + and CD8 + T cells and NK cells. However, the expression levels were less than 10% of each subset ( Figure 1G). Collectively, VIS-TA was highly expressed in kidney macrophages (R1 > R2), which remained consistent throughout the NTN model.
Role of VISTA in the NTN model. To explore the role of VIS-TA in the NTN model, we compared kidney status between WT and Vsir -/mice. At baseline (before induction), biochemical and histologic differences were not observed between kidneys in WT and Vsir -/mice (Supplemental Figure 1; supplemental material available online with this article; https://doi.org/10.1172/ JCI151189DS1). At the early phase after glomerular injury (i.e., day 8), the proteinuria and albuminuria amounts as glomerular injury markers were higher in Vsir -/mice than in WT mice ( Figure 2A). Other parameters related to the severity of nephrotic syndrome, such as hypoalbuminemia and hypercholesterolemia, were more severe in Vsir -/mice than in WT mice (Supplemental Figure 2). Markers of tubular injury, such as blood urea nitrogen and serum creatinine, became worse in Vsir -/mice than in WT mice ( Figure  2A). When histology was examined, Vsir -/mice had higher scores of glomerular and tubular injury than WT mice, which indicated that glomerular and tubular structural damage, such as crescents, tubular dilatation, and casts, was more frequently observed in Vsir -/mice than in WT mice ( Figure 2, B and C). The results of the TUNEL assay and kidney injury molecule-1 positivity supported more damage in Vsir -/mice than in WT mice ( Figure 2, D and E).
Changing characteristics of infiltrating T cells by VISTA depletion. VISTA on myeloid cells confers negative signals to the T cells in a contact manner (12)(13)(14)(15) because T cell proliferation and activation were reduced in VISTA-coated in vitro conditions compared with control-coated conditions (10,13,19). To evaluate the T cell status under in vivo NTN conditions, gene profiling was compared between WT and Vsir -/mice using single-cell RNA (scRNA) sequencing. Among immune cells, CD4 + and CD8 + T cells were clustered into non-effector memory-like (non-EM-like) and EM-like T cells ( Figure 3, A and B). The proportions of all clusters are shown in Figure 3C. The relative proportion of the EM-like subset per T cell lineage was higher in Vsir -/mice than in WT mice ( Figure 3C). EM-like CD4 + T cells of Vsir -/mice expressed Ifng and Il17a at higher levels than those of WT mice, whereas EM-like CD8 + T cells of Vsir -/mice expressed Ifng at higher levels than those of WT mice ( Figure 3D). The common changes in gene sets of T cell clusters in Vsir -/mice (vs. WT mice) were oxidative phosphorylation and fatty acid metabolism ( Figure 3E and Supplemental Figure 3). The tendencies of these metabolic features were positively correlated with Ifng levels in EM-like T cells ( Figure 3F). Because metabolic signatures are associated with specific immune cell fates and functions (20,21), metabolic deviation by depletion of VISTA might induce different cytokine profiles in T cells.
When these results were validated by flow cytometry, more CD4 + and CD8 + T subsets infiltrated the kidneys of Vsir -/mice than those of WT mice ( Figure 3G). When their production of cytokines was evaluated using flow cytometry, IFN-γ was primarily different between WT and Vsir -/mice, and its production was most attributable to CD8 + T cells (Figure 3, H and I). The use of VISTA-blocking antibody increased IFN-γ production from infiltrated T cells (Supplemental Figure 4), whereas the treatment with cytoplasmic autoantibody (ANCA) vasculitis also reflected this pattern such that VISTA expression in biopsied tissues was correlated with low tubulointerstitial fibrosis and improved patient outcomes. Collectively, our results indicate that VISTA, primarily expressed in kidney macrophages, is an inherent molecule that limits tubulointerstitial fibrotic transformation after acute glomerular injury.
Within the kidney, VISTA is known to be highly and constitutively expressed in R1 macrophages, but is low and inducible in other immune cell subsets, including R2 macrophages (10). When the transcription level of the Vsir gene (gene name of VISTA) was evaluated at the single-cell level (Figure 1, B-D), R1 macrophages had the highest expression, followed by R2 macrophages. Other cells, including T cells and CD45parenchymal tissue cells, had low and no expression of the Vsir gene, respectively.
After inducing NTN injury, approximately 50% of R1 macrophages had consistent expression of VISTA protein ( Figure 1E). Regarding R2 macrophages, all subsets had increased expression of VISTA except for the R2d subset. The distribution of macrophages within the kidney is shown in Figure 1F. When other immune cell resident R1 macrophages ( Figure 4D). In addition to the contact frequency, intercellular communication between macrophages and T cells was evaluated using ligand-receptor pairs from scRNA-sequencing data. The pair number among all macrophage and T cell clusters was 693 in Vsir -/mice, which was higher than the pair number of 163 in WT mice ( Figure 4E). This difference was most prominent at the ligand end of EM-like CD8 + T cells. Within the top 30 strong pairs, interactions between R1 macrophages and T cells were more identified in WT mice, whereas those between R2 macrophages and T cells were more identified in Vsir -/mice ( Figure 4F). When the interaction with EM-like CD8 + T cells was evaluated alone, the strongest pairs were B2m (EM-like CD8 + T) and Hfe (other R2) in WT mice and B2m (other R2) and Cd3g (EM-like CD4 + T) in Vsir -/mice ( Figure 4G and Supplemental Data 1). Collectively, the changes in contact frequency and intercellular communication in Vsir -/mice might affect the immunometabolic features of EM-like CD8 + T cells.
Fibrotic response of kidney tissue cells by VISTA depletion. The common final pathology after kidney inflammation is tubulointerstitial fibrosis (22,23). A consensus exists that infiltrated R2 macrophages inhibitors of oxidative phosphorylation and fatty acid metabolism decreased the production (Supplemental Figure 5), all of which supports the previous results. Collectively, cytokine profiling of T cells was altered in Vsir -/mice after NTN induction, and the most primary feature was high IFN-γ production by metabolically reprogrammed, EM-like CD8 + T cells.
Interaction between macrophages and T cells. The NTN model is known to be built by the stepwise effects of initial macrophages and subsequent infiltrated T cells (16). The present injury was also dependent on the T cell effect because kidney function was preserved in T cell-depleted mice compared with nondepleted mice (Supplemental Figure 6). Herein, we hypothesized that the contact frequencies between macrophages and T cells differed between WT and Vsir -/mice. R1 and R2 macrophages were detected as F4/80 + CD72 + and F4/80 + CD72cells, respectively, whereas T cells were defined as CD3 + cells in confocal images ( Figure 4, A and B). When the contact frequency was evaluated, Vsir -/mice had a higher density of macrophages around T cells than WT mice ( Figure 4C). The high contact frequency in Vsir -/mice was primarily attributable to infiltrating R2 macrophages compared with . KIM-1 + cells were calculated from 10 randomly selected images. Data are represented as mean ± SEM. P values were calculated using an unpaired Student's t test. *P < 0.05; **P < 0.01; ***P < 0.001. Data represent at least 3 independent experiments. play a role in inflammation-induced fibrosis (24,25), and subsequent activation of infiltrated T cells mediates its progression (26,27). Nevertheless, it is not completely understood which molecules are inherently protective or mediated in the pathologic process between glomerular injury and tubulointerstitial fibrosis. Vsir -/mice had a higher fibrotic area in the tubulointerstitium than WT mice ( Figure  5, A and B). α-Smooth muscle actin, a marker of myofibroblasts, was also more highly expressed in the tubulointerstitium of Vsir -/mice than in that of WT mice ( Figure 5C). To evaluate fibrosis-mediating factors in response to immune cell activity, the gene expression levels of several cytokines were compared between parenchymal tissue cells of WT and Vsir -/kidneys ( Figure 5D). Among them, Il9 was more highly transcribed in the parenchymal cells of Vsir -/mice, whereas Gzma was less transcribed in Vsir -/parenchymal cells than in WT cells. Levels of expression of other genes, such as Il4, Il12, Il13, and Tgfb1, seemed to be higher in Vsir -/mice than in WT mice, but statistical significance was not shown. The protein level of IL-9, which was primarily expressed in glomeruli, interstitium, and some tubules, was higher in the Vsir -/kidney than in the WT kidney (Figure 5E). The protein expression of the receptor for IL-9 did not differ between WT and Vsir -/kidneys (Supplemental Figure 7).
When the NTN-induced mice were followed up until the late phase (>1 month), the death rate was higher in the Vsir -/mice than in the WT mice ( Figure 6A). The biochemical and histological damage markers were worse in the Vsir -/mice than in the WT mice ( Figure 6, B-D). IFN-γ-producing CD8 + T cells were more highly identified in the Vsir -/mice than in the WT mice ( Figure 6, E and F). The IL-9 + and fibrotic areas were also larger in the Vsir -/mice than in the WT mice ( Figure 6, G-J). These results indicate that the IFN-γ/IL-9 axis was overwhelmed even in the late phase of Vsir -/mice compared with WT mice, which determined their tubulointerstitial fibrosis and kidney dysfunction.
Response of kidney tissues to IFN-γ and IL-9. To confirm the IFN-γ/IL-9 axis observed in Vsir -/mice, recombinant mouse IFN-γ (rmIFN-γ) and anti-IFN-γ antibodies were administered via subcapsular and intravenous injection, respectively, to NTN-induced mice. The rmIFN-γ-treated mice had higher kidney damage markers than vehicle-treated mice ( Figure 7A). rmIFN-γ treatment increased the IL-9 + area of the kidneys ( Figure 7B). The anti-IFN-γ antibody abrogated these pathologic changes (Figure 7, C and D). We further carried out adoptive transfer of T cells (from WT mice vs. Ifng -/mice) to the NTN-induced Rag1 -/mice, and their biochemical damage markers and IL-9 expression were compared (Figure 7, E and F). IFN-γ-producing T cells resulted in more damage and IL-9 production from the parenchyma than nonproducing T cells.
To confirm the IL-9/fibrosis axis observed in Vsir -/mice, recombinant mouse IL-9 (rmIL-9) and anti-IL-9 antibodies were administered via subcapsular and intravenous injection, respectively, to NTN-induced mice. The rmIL-9-treated mice had more fibrotic kidneys than vehicle-treated mice, although the differences in damage markers such as blood urea nitrogen, creatinine, and proteinuria were not prominent between the 2 groups ( Figure  7, G and H). When an anti-IL-9 antibody was used, all markers of damage and fibrosis were decreased (Figure 7, I and J). The reduction in histological injury scores by anti-IL-9 antibody was prominent in the tubulointerstitial compartment rather than in the glomerular compartment ( Figure 7, K and L). The number and proportion of infiltrated T cells were not different between mice administered control and anti-IL-9 antibodies ( Figure 7M). These results suggest that IL-9 affected tubulointerstitial fibrosis without changing the glomerular structure or T cell infiltration. Collectively, the IFN-γ/IL-9 axis participated in the progressive fibrosis of the tubulointerstitium after NTN induction, and VISTA may play a preventive role in this process as a sentinel molecule.
Impact of VISTA-depleted T cells in the model. VISTA is also expressed in naive T cells to maintain their quiescence and tolerance, which has been evaluated in lipopolysaccharide injection and graft-versus-host disease models (28). Because the protein expression of VISTA in mouse kidneys was expressed mostly in kidney macrophages (R1 > R2), the NTN results might be primarily attributable to the effects from the macrophage end rather than the T cell end. To determine the VISTA effect at the end of the T cell subset alone, NTN was induced in Rag1 -/mice, and the activity of adoptively transferred Vsir -/-T cells was evaluated in comparison with that of WT T cells. Referentially, adoptive transfer of T cells to NTN-induced Rag1 -/mice was sufficient to drive subsequent tubulointerstitial inflammation (Supplemental Figure 8), and the expression level of VISTA among adoptively transferred T cells was 4% (Supplemental Figure 9). The T cell numbers were not different between WT and Vsir -/mouse-derived T cells after NTN induction (Figure 8, A and B). The CD44 expression levels were also similar between the 2 cell groups (Figure 8, C and D). When competitive proliferation was evaluated in an in vivo model, the cell number and activation marker levels were not different between WT and Vsir -/mouse-derived T cells (Figure 8, E-G). The nonsignificant or minimal effects of VISTA at the end of the T cells might be because its protein expression level was very low in kidney-infiltrated T cells ( Figure 1G and Supplemental Figure 9).
IL-9 production in surrounding parenchymal tissue cells and aggravated interstitial fibrosis. The protective role of VISTA in tubulointerstitial fibrosis via the IFN-γ/IL-9 axis after glomerular injury could be reflected in human glomerulonephritis, wherein VISTA hi kidneys had low fibrosis and better prognosis than VISTA lo kidneys.
VISTA is an immunoregulatory and inhibitory checkpoint expressed in cells of the myeloid and lymphoid lineages (38). The expression can be inducible in inflammatory or cancerous conditions (12)(13)(14)(15), but an interesting aspect is its high expression in kidney-resident macrophages (10). When the expression level was compared among tissue-resident macrophages, the kidney-resident subset had the highest expression, followed by peritoneal, splenic, and bone marrow macrophages (10). These results indicate that the tissue environment may determine VISTA expression in macrophages, and the unique pattern of kidney-resident macrophages implies their homeostatic role under normal conditions or during kidney inflammation. Our previous work identified kidney-resident macrophages as playing a repair role after ischemic tubular damage, and VISTA was determined to be a molecule relevant to this repair role (10). The transition from acute glomerular injury to tubulointerstitial fibrosis was aggravated when VISTA was depleted, wherein immunometabolic changes in T cells were observed, such as augmented oxidative phosphorylation, fatty acid metabolism, and IFN-γ production. These changes may be dependent on tissue status or specific to diseases such as severe glomerulonephritis.
In addition to direct damage by immune cells, the responses of parenchymal tissue cells, including glomeruli, tubules, and other stromal cells, are important for determining kidney outcomes (39). Parenchymal tissue cell-derived cytokines can be inflammatory or antiinflammatory, and all of these cytokines participate in tubulointerstitial fibrosis as a repair or sometimes ongoing process (40,41). VISTA depletion augmented IFN-γ production from interstitial T cells, and then IL-9 was overwhelmed by surrounding parenchymal tissue cells. IL-9, as a Th2-type cytokine, has been related to immune tolerance and tissue fibrosis (42,43). IL-9 can be produced in kidneys after injury (44), but the subsequent pathophysiology by IL-9 is less understood than that in other organs, such as the lung and liver. The all-or-none status of IL-9 in transgenic and knockout mice results in unexpectedly reduced and increased inflammatory responses, respectively (45,46), indicating that proper or specific window levels may be needed to maintain homeostasis of the kidney or repair after injury. However, VISTA-depleted kidneys and subsequent high IFN-γ-producing T cells increased IL-9 levels in surrounding parenchymal tissue cells, which ultimately resulted in overzealous tubulointerstitial fibrosis.
VISTA can tune the activity of T cells in a contact manner, but there is a gap in understanding human kidneys. scRNA profiling indicated that C10orf54 was transcribed primarily in kidney MNPs and T cells, which was similar to the mouse counterpart. However, gene expression levels were different such that human monocyte-like MNPs (R2 or monocytes in the mouse kidney) had the highest expression levels among immune cell subsets, higher than those of R1-like MNPs (R1 in the mouse kidney). The expression level within kidneys was associated with the fibrotic outcomes of ANCA vasculitis, a severe form of glomerulonephritis. These results will help us understand the difference between mice and had a gene expression pattern similar to that of mouse R1 macrophages based on C1QC, APOE, CD74, and HLA-DRA (named R1-like MNPs), whereas the other had an expression pattern similar to that of mouse monocytes based on S100A8, S100A9, FCN1, VCAN, and IFITM2 (named monocyte-like MNPs; refs. 10, 30 and Supplemental Figure 10). Among them, monocyte-like MNPs had the highest expression, and R1-like MNPs ranked second. Among nonimmune cells, endothelial cells had high expression of C10orf54, but protein expression was not evident in human kidneys ( Figure 9C and Supplemental Figure 11). In humans, P-selectin glycoprotein ligand-1 (PSGL-1) is known to be a receptor for VISTA in acidic environments (33). When the gene expression of this receptor (named SELPLG) was profiled, CD4 + and CD8 + EM T cell clusters had the highest expression, followed by MNPs and NK cells ( Figure 9D). These results suggest that human kidney MNPs interact with other immune cells (particularly EM T cells) via a VISTA/PSGL-1 pair in acidic environments, such as glomerulonephritis (34). The gene expression profiles of other immune checkpoints in normal human kidney cells are shown in Figure 9D.
To translate the mouse results to human disease, we selected human cases with biopsy-proven ANCA vasculitis because both the histological (e.g., crescentic glomerulonephritis and tubulointerstitial fibrosis) and clinical (e.g., rapidly progressive glomerulonephritis) signs are the same as those observed in the NTN model (35)(36)(37). VISTA-producing cells were primarily identified in infiltrated immune cells ( Figure 9E). VISTA expression was negatively related to the IL-9 + and Sirius red + areas ( Figure 9F). When 23 samples were divided into 2 groups by the median value of expression (i.e., VISTA hi and VISTA lo kidneys), the VISTA hi group seemed to have a lower risk of renal progression than the VISTA lo group ( Figure 9G). These results indicate that VISTA could be a biomarker related to glomerulonephritis and its fibrotic outcome.

Discussion
Tubulointerstitial fibrosis after glomerular injury determines patient outcomes, but its immunological link and relevant sentinel molecules are not completely understood. The present results may provide clues, and VISTA was identified as a sentinel molecule particularly expressed in kidney macrophages. If VIS-TA was not expressed in the kidney, immunometabolic changes occurred, such as high oxidative phosphorylation and fatty acid metabolism and IFN-γ overproduction. These changes provoked For the NTN model, mice were preimmunized with 200 μg of sheep immunoglobulin G in Freund's complete adjuvant via the intraperitoneal route, followed by 5 μL/g sheep nephrotoxic serum (Probetex Inc.) via intravenous injection 4 days later. To evaluate the IFN-γ/IL-9 axis, recombinant proteins (5 ng of IFN-γ or IL-9) were treated via subcapsular injection at day 7 after NTN induction, and antibodies (1 mg of anti-IFN-γ or anti-IL-9 antibody) were administered via intravenous injection at day 0 of NTN induction. As a metabolic inhibitor, 10 ng of oligomycin (Sigma Aldrich) or etomoxir (Sigma Aldrich) was administered via subcapsular injection at day 7 humans and could improve intervention strategies related to VIS-TA or kidney immune cells.
A clear understanding of the pathogenesis of glomerulonephritis will provide valuable insight into disease progression and options for intervention. The present study shows that VISTA, which is primarily expressed in kidney macrophages, has a protective role in tubulointerstitial fibrosis after acute glomerular injury and that IFN-γ and IL-9 are involved in the pathological process. VISTA, as an immunoregulatory sentinel molecule, may be highlighted in future biomarker research and therapy development.
staining, cells were incubated with fixation-permeabilization buffer, washed with permeabilization buffer (Fixation/Permeabilization Solution Kit; BD Biosciences), and then incubated with antibodies against intracellular antigens. Samples were processed by a BD Fortessa (BD Biosciences) and analyzed with FlowJo software. The antibodies used for flow cytometry are listed in Supplemental Table 1.
after NTN induction. The mice were sacrificed at the indicated time points after reperfusion.
using the Imaris program (version 9.3.1; Bitplane). The colocalization module (Coloc in Imaris) was used to label CD3 and DAPI for T cells and F4/80 and CD72 for kidney-resident macrophages. Surfaces and spots were created for T cells and macrophages, and the number of spots was calculated within the indicated distance from the surface. The antibodies used for immunofluorescence are listed in Supplemental Table 1.
Immunofluorescence. Paraffin-embedded tissue sections were deparaffinized and rehydrated with xylene and ethanol. After retrieval of antigens, sections were blocked in 0.1 M Tris containing 0.1% Triton X-100, 10% normal mouse serum, and 1% bovine serum albumin. Images were acquired using a Leica DMi8 microscope (Leica Microsystems). The contact analysis between macrophages and infiltrated T cells was performed . P values were calculated using an unpaired Student's t test. All the differences between groups were not significant.
Leica). The antibodies used for immunofluorescence are listed in Supplemental Table 1.
Real-time qPCR. RNA was purified from tissues using a Direct-zol RNA MicroPrep Kit (Zymo Research). RNA was reverse transcribed to cDNA with a PrimeScript RT Reagent Kit (TaKaRa Bio Inc.). Gene expression was evaluated by real-time reverse-transcriptase PCR Immunohistochemistry. The steps before blocking were the same as those described in the immunofluorescence section. Blocking reagent was added for 1 hour at room temperature. Images were obtained using a Leica TCS SP8 STED CW (Leica Microsystems). All morphometric parameters were determined using a microscope coupled to a computerized morphometry system (Qwin3, border loss, and necrosis as follows: 0, no involvement; 1, less than 10% involvement; 2, 10%-25% involvement; 3, 25%-50% involvement; 4, 50%-75% involvement; and 5, more than 75% involvement. Ten random fields per kidney section (×200 magnification) were used for quantification. Sirius red (Abcam) and Masson's trichrome (Roche) staining assays were performed according to the manufacturers' recommendations. Apoptotic cells were identified in tissue sections using the Click-iT TUNEL imaging assay (Thermo Fisher Scientific) according to the manufacturer's instructions. The areas of fibrosis and positive staining were evaluated using ImageJ software (version 1.5; NIH).
Human samples. Kidney biopsied tissues were evaluated in patients with ANCA vasculitis (n = 23). Immunohistochemistry and Sirius red staining were used to estimate the VISTA + , IL-9 + , and fibrotic areas in the interstitium of the cortex. Composite renal risk (e.g., doubling of serum creatinine, development of end-stage renal disease, and death) was compared between the VISTA hi and VISTA lo groups. Normal human kidney tissue was obtained from patients who underwent radical nephrectomy due to urogenital malignancy, but did not have hydronephrosis or any infectious diseases.
Statistics. All analyses and calculations were performed using GraphPad Prism (version 8.0; GraphPad Software). The results are expressed as the mean ± SEM or proportion. Differences between groups were evaluated using 2-tailed Student's t test and ANOVA with Tukey's test for comparison between 2 and multiple groups, respectively. Survival curves were drawn using the Kaplan-Meier method. To compare survival curves between groups, the log-rank test was applied. A P value of less than 0.05 was considered statistically significant.
Study approval. All animal experiments were approved by the Seoul National University IACUC (no. SNU-190621-3-13). The study design for human samples was approved by the IRB of Seoul National University Hospital (H-1810-016-975) and complied with the Declaration of Helsinki. All patients provided written, informed consent for the donation and use of their specimens. (0420190660 to SSH). The human biospecimens were provided by the Biobank of Seoul National University Hospital, a member of using iQ SYBR Green Supermix (Bio-Rad) on a PCR amplification and detection instrument (CFX Connect Real-Time PCR Detection System; Bio-Rad). Gene expression was normalized to 18S rRNA, and the mean relative gene expression was calculated using the 2 -ΔΔCt method. The primers used are listed in Supplemental Table 2.
Single-cell RNA sequencing. After digesting kidneys with 0.2 mg/ml liberase (Roche) at 37°C for 30 minutes, CD45 + cells were flow cytometrically sorted for the subsequent process. Libraries were prepared using the chromium controller according to the 10× Chromium Next GEM Single Cell 3′ protocol (version 3.1; 10× Genomics). Briefly, the cell suspensions were diluted in nuclease-free water to achieve a target count of 10,000. The cell suspension was mixed with master mix and loaded with gel beads and partitioning oil into a Chromium Next GEM Chip G. RNA transcripts were uniquely barcoded and reverse-transcribed within droplets. The cDNA molecules were pooled and subjected to an end-repair process, the addition of a single A base, and ligation of the adapters. The products were purified and enriched using PCR to produce the final cDNA library. The purified libraries were quantified using quantitative PCR (qPCR) according to the manufacturer's protocol (Sigma-Aldrich) and were qualified using the Agilent 4200 TapeStation (Agilent Technologies) and sequenced using HiSeqX (Illumina) with a read length of 28 bp for read 1 (cell barcode and UMI), an 8 bp index read (sample barcode), and a read length of 91 bp for read 2 (RNA read). The Cell Ranger pipeline (version 3.1.0; 10× Genomics) was used to process the raw data set.
As a quality control of pooled scRNA-sequencing data of normal mouse kidneys (30,47,48), genes expressed in 10 or more cells, cells with 200-4000 unique genes, and cells with 20% or more mitochondrial genes were used. In the flow cytometrically sorted immune cells for comparison between NTN-induced WT and Vsir -/mice, genes expressed in 5 or more cells, cells with 200 or more UMI counts, and cells with 10% or fewer mitochondrial genes were selected. As a quality control of pooled scRNA-sequencing data of normal human kidneys (29)(30)(31)(32), the same quality control as in the NTN model was used. The raw data on normal mouse and human kidneys could be identified in the original papers, and the data on NTN-induced kidneys were deposited in the NCBI's Gene Expression Omnibus database (GEO GSE181163). R (version 4.0.3; The Comprehensive R Archive Network: http:// cran.r-project.org) and Seurat (version 3.2.3) packages were used in analyses, as follows: SCTransform, merging data with adjusting batch-effects (49); FindNeighbors and FindClusters, finding clusters; RunUMAP, FeaturePlot, DotPlot, and VlnPlot, visualizing data; Findmarkers, identifying differentially expressed genes; fgsea, analyzing the Hallmark gene set enrichment analysis; and SingleCellSignalR, evaluating the ligand-receptor interaction (50).
Kidney histology. Kidneys were fixed in 4% formalin, paraffin embedded, and cut into 4 μm sections. Sections were then stained with periodic acid-Schiff before microscopy analysis (Leica Microsystems). Glomerular injury was estimated in a blinded manner based on the following system: 0, normal glomeruli without structural damage; 1, glomerular matrix expansion and edema formation of less than 25% of the glomeruli; 2, increased intraglomerular cell count and swelling up to 50%; 3, obliteration or collapse in up to 75% of glomeruli; and 4, complete structural obliteration and thrombosis (51). The assessment of tubular injury in the cortex was graded in a blinded manner based on the percentages of tubular dilatation, cast deposition, brush