Basic Research

CD103+ Kidney Dendritic Cells Protect against Crescentic GN by Maintaining IL-10–Producing Regulatory T Cells

Beatrix D.G. Evers, Daniel R. Engel, Alexander M.C. Böhner, André P. Tittel, Torsten A. Krause, Christoph Heuser, Natalio Garbi, Wolfgang Kastenmüller, Matthias Mack, Gisa Tiegs, Ulf Panzer, Peter Boor, Isis Ludwig-Portugall and Christian Kurts
JASN November 2016, 27 (11) 3368-3382; DOI: https://doi.org/10.1681/ASN.2015080873

This article requires a subscription to view the full text. If you have a subscription you may use the login form below to view the article. Access to this article can also be purchased.

Abstract

Kidney dendritic cells (DCs) regulate nephritogenic T cell responses. Most kidney DCs belong to the CD11b+ subset and promote crescentic GN (cGN). The function of the CD103+ subset, which represents <5% of kidney DCs, is poorly understood. We studied the role of CD103+ DCs in cGN using several lines of genetically modified mice that allowed us to reduce the number of these cells. In all lines, we detected a reduction of FoxP3+ intrarenal regulatory T cells (Tregs), which protect against cGN. Mice lacking the transcription factor Batf3 had a more profound reduction of CD103+ DCs and Tregs than did the other lines used, and showed the most profound aggravation of cGN. The conditional reduction of CD103+ DC numbers by 50% in Langerin-DTR mice halved Treg numbers, which did not suffice to significantly aggravate cGN. Mice lacking the cytokine Flt3L had fewer CD103+ DCs and Tregs than Langerin-DTR mice but exhibited milder cGN than did Batf3−/− mice presumably because proinflammatory CD11b+ DCs were somewhat depleted as well. Conversely, Flt3L supplementation increased the number of CD103+ DCs and Tregs, but also of proinflammatory CD11b+ DCs. On antibody-mediated removal of CD11b+ DCs, Flt3L supplementation ameliorated cGN. Mechanistically, CD103+ DCs caused cocultured T cells to differentiate into Tregs and produced the chemokine CCL20, which is known to attract Tregs into the kidney. Our findings show that CD103+ DCs foster intrarenal FoxP3+ Treg accumulation, thereby antagonizing proinflammatory CD11b+ DCs. Thus, increasing CD103+ DC numbers or functionality might be advantageous in cGN.

Dendritic cells (DCs) populate virtually all organs, including the kidney. Together with macrophages, they constitute the renal mononuclear phagocyte system,1,2 which alerts the immune system to the presence of tissue injury,3 infection,4 or crystal formation that triggers inflammasome activation.5 Being professional antigen–presenting cells, kidney DCs capture antigens and transport them to draining lymph nodes to present them to naive T cells.6 In the absence of pathogen– or danger–associated molecular patterns, kidney DCs tolerate naive T cells, whereas the presence of such patterns causes kidney DCs to mature, thereby acquiring the capacity to activate T cells.7,8 Some kidney DCs do not leave the kidney and regulate infiltrating effector Th cells. In murine models of human crescentic GN (cGN), such as nephrotoxic serum nephritis, kidney-resident DCs initially display an anti-inflammatory role,9 which includes the recruitment of regulatory iNKT cells.10 Later, when inflammation becomes chronic, DCs mature and produce chemokines and cytokines that attract and stimulated Th1 and Th17 cells, resulting in a mononuclear tubulointerstitial infiltrate that drives disease progression.7 From day 7 after cGN induction, FoxP3+ regulatory T cells (Tregs) play another important counter–regulatory role, and Treg depletion aggravated cGN.11–13 The suppressive mechanism used by Tregs is not exactly clear but involves the immunosuppressive cytokine IL-10.14 The recruitment of Tregs into the nephritic kidney requires the chemokine receptor CCR6 on Tregs,15 but it is unclear which cell produces CCL20, the only known CCR6 ligand.16

More than 90% of kidney DCs belong to a DC subset characterized by expression of the integrin CD11b and the chemokine receptor CX3CR1, which shares phenotypic and functional characteristics with tissue macrophages.17–19 There is another subset of tissue DCs characterized by expression of the integrin CD103 that is not considered to overlap with macrophages.18,20–22 In the lung, liver, or intestine, CD103+ DCs constitute 20%–50%, whereas they represent a minority of <5% of DCs in the kidney.20 Their development depends on the transcription factor Batf3 and the hematopoietic growth factor Flt3L, whereas CD11b+ DCs largely depend on the NF-κB component RelB and only partially depend on Flt3L.20,23–26 In lymphatic tissues, Batf3-dependent DCs express CD8 instead of CD103.27 Batf3-dependent DCs are best known for their ability to produce IL-1228 and crosspresent antigen to CD8+ T cells.27,29–31 These T cells are important for the antiviral defense but may also cause immune-mediated diseases, such as type 1 diabetes mellitus32 and perhaps, FSGS.33 In the intestine, CD103+ DCs served classic DC functions in the induction of adaptive immunity after migration to draining lymph nodes.34,35 However, they induced Treg differentiation ex vivo, suggesting that they might regulate tissue homestasis.36–38 However, experimental evidence supporting this notion is lacking, and Batf3−/− mice that lack CD103+ DCs showed unaltered inflammatory bowel disease.39 The role of renal CD103+ DCs is poorly understood. Here, we addressed this question in cGN and discovered an immunoregulatory role of these DCs in the kidney.

Results

CD103+ DCs Accumulate in the Kidney during cGN

We induced cGN in C57BL/6 wild–type (WT) mice and enumerated DC subsets in kidney single–cell suspensions from healthy and nephritic mice at different time points using flow cytometry. Although CD103+ DCs represented a minority among the renal immune cells under homeostatic conditions, they accumulated appreciably during cGN (Figure 1B). The numbers of CD103+ DCs did not change much in the first 4 days of cGN but more than tripled between days 4 and 10, peaking at day 7 (Figure 1C). CD11b+ DCs increased similarly (Figure 1D) as described before.2 These results showed that not only CD11b+ DCs but also, CD103+ DCs accumulate in kidney inflammation, suggesting that the latter might play a functional role from day 7 onward.

Figure 1.
Figure 1.

CD103+ DCs accumulate in the kidney in cGN. (A) Gating strategy of kidney DC subsets defined as CD11c+ MHC II+ cells and subset analysis on the basis of CD11b and CD103. (B) Representative flow cytometric analysis of mice before (control [Ctrl.]) and 4 (d4) and 7 days (d7) after NTS injection. Quantification of (C) renal CD103+ DCs and (D) CD11b+ DCs in nephritic WT mice. Results represent two to four experiments, with 4–12 mice per group. Statistical significance was tested with the Kruskal–Wallis test with Dunn's multiple comparison test. *P<0.05; **P<0.01; ***P<0.001.

CD103+ DCs Are Protective in cGN

To clarify the role of CD103+ DCs in cGN, we used Batf3−/− mice, which lack these DCs but not CD11b+ DCs.26 Healthy Batf3−/− mice do not show spontaneous renal pathology.26 We first verified that CD103+ DC numbers were reduced by 99.9% in kidneys of nephritic Batf3−/− mice, whereas CD11b+ DC numbers were unchanged (Figure 2A). On day 7 after disease induction, cGN was notably aggravated in Batf3−/− mice compared with WT controls, which was evident by diminished creatinine clearance and a tendency toward higher proteinuria (Figure 2, B and C). Compared with WT mice, the histologic analysis showed significantly increased numbers of glomeruli with extracapillary proliferates, which were more severe (e.g., often circumferential in Batf3−/− versus segmental in WT mice) (Figure 2, D and E). On day 12 of cGN, kidney function was even more reduced (Figure 2, F and G). Histologic analysis revealed more severe glomerular damage (Figure 2, H and I). These results indicated that CD103+ DCs are protective in cGN.

Figure 2.
Figure 2.

Batf3 deficiency aggravates cGN. (A) Percentages and absolute cell counts of CD103+ DCs and CD11b+ DCs in WT and Batf3−/−mice 7 days after cGN induction. (B and F) Creatinine clearance, (C and G) albuminuria, and (D and H) percentage of crescentic glomeruli in WT and Batf3−/− mice (A–E) 7 and (F–I) 12 days after NTS challenge. (E and I) Representative periodic acid–Schiff– (PAS) or Gömöri Methamine silver–stained histologic sections. Results are combined from two to three individual experiments, with 5–12 mice per group. Significance was tested by two–tailed Mann–Whitney U test. Scale bars, 50 μm. *P<0.05; **P<0.01; ***P<0.001.

Reduced IL-10 Production in Nephritic Batf3−/− Mice

When we analyzed parameters for intrarenal inflammation, we noted higher levels of the proinflammatory cytokine TNFα and a trend toward higher levels of IL-6 and more IFNγ–producing Th1 cells (Figure 3A). Although the anti–inflammatory cytokine TGFβ was unchanged, IL-10 was markedly reduced (Figure 3B). IL-10 plays an important regulatory role in cGN, and it can be produced by Tregs in this model.14

Figure 3.
Figure 3.

Reduced intrarenal anti-inflammatory cytokine production in nephritic Batf3−/− mice. (A) Concentrations of TNFα and IL-6 in supernatants of kidneys of nephritic Batf3−/− and WT mice measured by bead assay. Intracellular staining for IFNγ in CD45+ CD4+ TCRβ+ cells from kidney single–cell suspensions. (B) Quantitative RT-PCR analysis of TGFβ and IL-10 expression in kidneys from nephritic WT and Batf3−/− mice 7 days after cGN induction. mRNA levels are expressed as x-fold of healthy controls. (C) Tregs from kidneys of Foxp3IRES-mRFP × IL-10 ires gfp–enhanced reporter (Fir/Tiger) mice were stained for CD4+ and RFP+, indicating Foxp3+ cells; DCs were stained for MHC II+ CD11c+ and further subdivided into CD103+ and CD11b+ DCs. Representative contour plots depicting IL-10− and IL-10+ Tregs, IL-10− and IL-10+ CD103+ kidney DCs, and IL-10− and IL-10+ CD11b+ kidney DCs. (D) Absolute numbers of renal IL-10+ Foxp3+ Tregs, IL-10+ CD103+ kidney DCs, and IL-10+ CD11b+ kidney DCs. (E) IL-10 production measured by bead assay in supernatants of FACS–sorted CD103+ DCs, CD11b+ DCs, and CD45– nonimmune cells from WT mice 7 days after cGN induction. Data are representative of two independent experiments using (A–D) four to eleven or (E) 10 mice per group. Statistical significance was tested by (A and B) two–tailed Mann–Whitney U test or (D and E) Kruskal–Wallis test with Dunn's multiple postcomparison test. Ctrl., control; n.d., not detectable. *P<0.05; **P<0.01.

We determined the cellular source of IL-10 in cGN with the use of double–knockin reporter mice (Foxp3IRES-mRFP × IL-10 ires gfp–enhanced reporter), which allow sensitive simultaneous detection of IL-10 (GFP+) and FoxP3 (mRFP+). Phenotypic characterization of mRFP+ Tregs revealed expression of CCR6 (Supplemental Figure 1), consistent with its reported function to recruit Tregs into the kidney.15 Furthermore, we detected the transcription factors helios and neuropilin, suggesting thymic derivation, the IL-10 receptor, ICOSL, and CTLA-4 but not LAG3 (Supplemental Figure 1). IL-10 was detectable in intrarenal FoxP3+ Tregs, as expected, and also, CD103+ DCs were positive, but there were no IL-10+ CD11b+ DCs (Figure 3C). IL-10+ Tregs were more numerous than IL-10+ CD103+ DCs (Figure 3D). These results suggests that CD103+ DCs maintain intrarenal IL-10 production indirectly via Tregs and to a smaller extent (also directly), by producing IL-10 themselves.

Reduction of Renal FoxP3+ Tregs but Not iNKT Cells in Nephritic Batf3−/− Mice

Tregs are potent anti–inflammatory regulators in cGN.11–13 When we enumerated FoxP3+ Tregs on day 7 of cGN, they were 65% less numerous in kidneys of Batf3−/− mice compared with WT controls (Figure 4, A and B). By contrast, in CX3CR1GFP/GFP mice, which lack renal CD11b+ DCs40 but not CD103+ DCs, Treg numbers were unaltered (Figure 4C), indicating that CD103+ DCs but not CD11b+ DCs regulate intrarenal Treg numbers.

Figure 4.
Figure 4.

Protective FoxP3+ Tregs but not iNKT cells are diminished in nephritic Batf3−/− mice. (A and B) Intrarenal Tregs detected by flow cytometry on day 7 after cGN induction. A shows representative contour plots, and B shows absolute numbers of CD4+ FoxP3+ Tregs per kidney. (C) Quantification of renal CD11b+ DCs, CD103+ DCs, and FoxP3+ Tregs in WT and CX3CR1GFP/GFP mice 7 days after cGN induction. (D) Representative flow cytometry contour plots and absolute numbers of α-GalCer+ TCRβ+ NKT cells in WT and Batf3−/− mice on day 7 after cGN induction. Results are combined from two to three individual experiments, with five to eight mice per group. Statistical significance was tested with the two–tailed Mann–Whitney U test. *P<0.05; **P<0.01.

We next asked whether CD103+ DCs also regulate the other previously described renoprotective T cell subsets, iNKT cells.10 Intrarenal CD1d–tetramer+ TCRβ+ was not significantly reduced in Batf3−/− compared with WT mice (Figure 4D), arguing against an impaired anti–inflammatory iNKT cell response in the absence of CD103+ DCs. It has to be kept in mind that this experiment does not permit conclusions on the baseline activation status of iNKT cells or their immunosuppressive capacity and therefore, does not absolutely exclude a role of iNKT cells in Batf3−/− mice. Nevertheless, these results support a role of CD103+ kidney DCs in the maintenance of FoxP3+ Tregs but not iNKT cells.

No Influence of Batf3 Deficiency on Systemic Nephritogenic Immune Responses

The reduction of intrarenal Tregs might theoretically result from a systemic reduction of these cells in Batf3−/− mice. We, therefore, enumerated Tregs in the spleen and excluded this alternative explanation by showing unchanged numbers of FoxP3+ Tregs in nephritic WT and Batf3−/− mice (Figure 5A). Likewise, numbers of splenic IFNγ+ CD4+ Th1 cells, CD11b+ DCs, and F4/80+ macrophages were unaltered, whereas CD8+ DCs were almost absent in spleens of Batf3-deficient mice (Figure 5A).

Figure 5.
Figure 5.

Batf3-deficiency does not affect the systemic nephritogenic immune response. (A) Quantification of splenic FoxP3+ Tregs, IFNγ+ CD4+ Th1 cells, CD11b+ DCs, F4/80+ macrophages, and CD8+ DCs 7 days after NTS challenge. (B) Concentrations of TNFα and IFNγ in supernatants of kidneys of nephritic WT and Batf3−/− mice measured by bead assay. (C) Titers of mouse anti–sheep IgG and isotypes of IgG1 and IgG2a were measured in sera by ELISA. Analyses were performed 7 days after cGN induction. Results were combined from two experiments, with 4–11 mice per group. Statistical significance was tested with the two–tailed Mann–Whitney U test. ***P<0.001.

To corroborate these findings, we asked whether Batf3−/− mice mounted a stronger nephritogenic immune response in cGN. To address this possibility, we isolated splenocytes from nephritic WT and Batf3−/− mice and restimulated them in vitro with nephrotoxic sheep serum. Cytokine analysis of supernatants showed no significant difference in the production of TNFα and IFNγ between the two groups (Figure 5B). As another parameter for the nephritogenic Th cell response, we measured serum antibody titers against sheep Ig, the nephritogenic antigen planted into the kidney. Titers of sheep Ig–specific IgG1, characterizing Th2 responses, and specific IgG2a, characterizing Th1 responses, were not altered between WT and Batf3−/− mice (Figure 5C). Taken together, these data argued against an intensified systemic humoral or cellular immune response in nephritic Batf3−/− mice. Thus, a local effect of renal CD103+ DCs likely affected cGN in the kidneys of these mice.

Depletion of CD103+ DCs Reduces Intrarenal Tregs

To corroborate this interpretation, we decided to deplete CD103+ DCs with the use of Langerin–diphtheria toxin receptor (DTR) mice. Langerin is expressed by renal CD103+ DCs but not by CD8+ DCs,20 the Batf3–dependent DC type in lymphatic tissues where systemic immune responses are induced.27 Therefore, Langerin-DTR mice allow us to distinguish between the roles of CD103+ kidney DCs and CD8+ splenic DCs. We induced cGN in these mice and depleted CD103+ DCs every second day by injecting diphtheria toxin (DT). As controls, WT mice were treated with the same amount of DT. On day 7 of nephritis, numbers of CD103+ kidney DCs in Langerin-DTR mice were 50% reduced (Figure 6A), whereas the numbers of CD11b+ kidney DCs were not significantly changed (WT, 272,571±38,473; Langerin-DTR, 198,501±42,613; n=4; P>0.05). Intrarenal Treg numbers were reduced by about 50% as well (Figure 6B). Creatinine clearance seemed to be lower in mice depleted of CD103+ DCs, albeit not to a statistically significant level (Figure 6C). Crescent formation was not different (Figure 6D). The less pronounced disease aggravation in Langerin-DTR mice compared with Batf3-deficient mice is likely because of the reduction of CD103+ DCs by only 50% in the former compared with >99% in the latter. Nevertheless, these findings supported the linkage between CD103+ DCs and Tregs and argued against a role of CD8+ lymphatic tissue DCs in the regulation of intrarenal Tregs.

Figure 6.
Figure 6.

Conditional depletion of CD103+ DCs reduces Tregs. Numbers of (A) CD103+ DCs and (B) Tregs, (C) creatinine clearance, (D) percentage of crescentic glomeruli, and representative immunohistology in Langerin-DTR or WT mice 7 days after cGN induction that were injected with DT on days −1, 1, 3, and 5 after cGN induction. Results are representative for two experiments, with four mice per group. Statistical significance was tested with the unpaired t test. Scale bars, 50 μm. *P<0.05.

Aggravated cGN Severity and Fewer Intrarenal FoxP3+ Tregs in Flt3L-Deficient Mice

Because the aggravation of cGN in Langerin-DTR mice was not pronounced enough, we wished to corroborate the protective role of CD103+ DCs by using another mouse line harboring fewer of these cells. To this end, we induced cGN in Fl3L−/− mice, in which CD8+ and CD103+ DCs are reduced in other tissues.20,41 We first determined that CD103+ DCs were reduced in kidneys of nephritic Fl3L−/− mice by >80% (Figure 7A). We also noted a significant reduction of CD11b+ DCs, albeit to a lesser extent (Figure 7B). Intrarenal FoxP3+ Tregs were decreased by >50% in nephritic Flt3L−/− mice compared with WT controls (Figure 7C), whereas renal iNKT cells were not significantly altered (WT, 23,260±10,322; Flt3L−/−, 22,983±5608; n=3; P>0.05), matching the observations in Batf3−/− mice (Figure 4D). Creatinine clearance was lower in Flt3L−/− mice than in WT controls (Figure 7D). Albuminuria and glomerular crescents, however, did not statistically differ between nephritic WT and Flt3L−/− mice 7 days after disease induction (Figure 7, E and F). The less severe phenotype in Flt3L−/− mice might be explained by the previous finding that this cytokine also fosters CD11b+ DCs, albeit not as effectively as CD103+ DCs.25

Figure 7.
Figure 7.

Flt3L−/− mice harbor less intrarenal Treg and show aggravated cGN (A) CD103+ DCs, (B) CD11b+ DCs, (C) CD4+ FoxP3+ Tregs, (D) creatinine clearance, (E) albuminuria, (F) proportion of crescentic glomeruli, and (G) representative periodic acid–Schiff–stained histologic images of glomeruli 7 days after cGN induction in WT and Flt3L−/− mice. Results are combined from three individual experiments, with 6–13 mice per group. Statistical significance was tested with the two–tailed Mann–Whitney U test. Scale bars, 50 μm. *P<0.05; **P<0.01; ***P<0.001.

Flt3L Supplementation Increases Intrarenal Tregs and Attenuates cGN When Combined with Depletion of CCR2+ CD11b+ DCs

Previous studies have applied Flt3L to increase protective CD103+ DC numbers in the intestine and succeeded to attenuate experimental inflammatory bowel disease.42 When we used this strategy in cGN, Flt3L, indeed, increased numbers of renal CD103+ DCs and Tregs (Figure 8, A and B). However, CD11b+ DCs were increased (Figure 8C), which is consistent with previous studies showing that Flt3L also exerts a minor effect on CD11b+ DCs.20,23–25 This increase might counteract that of CD103+ DCs, which may explain why disease severity was unaltered (Figure 8D).

Figure 8.
Figure 8.

Flt3L increases renal CD103+ DCs and Tregs and attenuates cGN when inflammatory DCs are removed. (A–D) Melanoma cells (5×105) expressing Flt3L or OVA as a control were implanted subcutaneously into mice, and on day 9, cGN was induced. After another 7 days, (A) renal CD103+, (B) Tregs, (C) CD11b+ DCs, and (D) creatinine clearance were determined. (E–K) Same experiment as in A–D, except that inflammatory CD11b+ DCs were depleted using CCR2 antibodies. (E) Renal CD103+, (F) Tregs, (G) CD11b+ DCs, (H) creatinine clearance, (I) albuminuria, and (J) the proportion of crescentic glomeruli were determined. K shows representative histologic images stained by Gömöri Methamine silver. Results are representative of two individual experiments, with four to six mice per group in each experiment. Statistical significance was tested with the two–tailed Mann–Whitney U test. Scale bars, 50 μm. *P<0.05; **P<0.01.

To overcome this problem, we decided to remove the recruited CD11b+ DCs with the use of CCR2 antibodies, which specifically targets inflammatory myeloid cells but not T cells.43 Also, under these conditions, Flt3L supplementation increased CD103+ DCs and Tregs (Figure 8, E and F), but the number of CD11b+ DCs did not increase (Figure 8G). Indeed, creatinine clearance was higher and albuminuria was lower in mice supplemented with Flt3L (Figure 8, H and I). The proportion of crescentic glomeruli was not altered (Figure 8J), despite the histologic impression of improved morphology (Figure 8K). These findings showed that increasing only CD103+ DCs but not CD11b+ DCs increases renal Tregs and attenuates renal function in cGN.

CD103+ Kidney DCs Can Induce FoxP3+ Tregs and Produce the Treg–Recruiting Chemokine CCL20 Ex Vivo

To understand how CD103+ kidney DCs sustain intrarenal Tregs, we flow sorted CD103+ and as a control, CD11b+ kidney DCs and cocultured them with naive specific Th cells and antigen in vitro. As a model antigen, we used OVA, and as OVA–specific T cells, we used the well established DO11.10 transgenic T cells, which in contrast to OT-II cells, can be readily transformed into Tregs.44 We crossed DO11.10 to DEREG mice that express a GFP reporter for FoxP3 to conveniently detect Treg conversion by measuring FoxP3 induction. Furthermore, DEREG mice allow for depletion of preexisting Tregs by injecting DT. This allows for the conclusion that FoxP3+ cells have arisen from naive Th cells and have not by expansion of preexisting Tregs from the donor mice. When we analyzed these cocultures, CD103+ kidney DCs but not CD11b+ kidney DCs readily induced differentiation of sorted naive CD4+ T cells into FoxP3+ CD25+ Tregs (Figure 9, A and B). In contrast, CD11b+ kidney DCs induced more Th effector cells identified as CD4+ CD25+ FoxP3− DO11.10 cells (Figure 9C).

Figure 9.
Figure 9.

CD103+ kidney DCs can induce FoxP3+ Tregs and produce the Treg–attracting chemokine CCL20. (A–C) Kidney single–cell suspensions from C57BL/6xBALB/c mice 1 hour after ip injection of 700 μg OVA per mouse were stained for MHC II+ CD11c+ DCs and sorted according to CD103 and CD11b expression 7 days after cGN induction; 2×104 CD103+ or CD11b+ kidney DCs were cultured with 4×104 DO11.10 × DEREG CD4+ T cells purified from DT-treated mice. Shown are (A) absolute numbers of CD4+ FoxP3+ CD25+ KJ126+ Tregs after 6 days and (B) their intracellular FoxP3 expression and (C) absolute numbers of CD4+ FoxP3– CD25+ KJ126+ effector Th cells. Cytokine-induced Tregs served as positive controls. Negative controls were unstimulated T cells. (D–F) CCL20 protein expression shown as (D) representative histograms and (E) MFI of flow cytometric analysis or (F) ELISA analysis of culture supernatants of sorted cells from mice 7 days after cGN induction. Splenic DCs stimulated with LPS for 2 hours served as positive controls for the staining, and negative controls were stained using isotype antibodies. (G) CCL20 mRNA levels in WT and Batf3−/− mice 7 days after cGN induction. Statistical significance was tested using (A–F) Kruskal–Wallis test with Dunn's multiple comparison test and (G) unpaired t test. contr., Control; neg., negative; pos., positive. *P<0.05.

Finally, we wondered whether CD103+ DCs might be able to recruit Tregs into the kidney. Because the chemokine receptor CCR6 on Tregs is essential for such recruitment,15 we stained CD11c+ MHC II+ kidney DCs from nephritic mice for the only known CCR6 ligand, CCL20.16 Indeed, among the CD103+ DCs, we noted a subset that produced considerable levels of this chemokine, whereas no CD11b+ DCs did so (Figure 9, D and E). When we isolated CD103+ DCs from nephritic kidneys, CCL20 was secreted into the supernatant by CD103+ DCs but not by CD11b+ DCs (Figure 9F). CCL20 was also produced by nonhematopoietic cells (Figure 9F). CCL20 levels in nephritic kidneys were reduced in Batf3−/− mice compared with WT controls (Figure 9G), showing that CD103+ DCs contributed a significant part of chemokine production in cGN. These findings suggest that CD103+ kidney DCs might regulate Tregs by inducing their differentiation and/or recruiting them into the nephritic kidney.

Discussion

Tissue DCs of both the CD11b+ and the CD103+ subsets are being studied extensively in many disease settings. The CD103+ DC subset is remarkably rare in the kidney, compared with other organs.20 Previous studies on kidney DCs mainly examined CD11b+ kidney DCs.19 Here, we focused on CD103+ DCs and their role in cGN by using a variety of genetic tools. We found that cGN was severely aggravated in mice that lack CD103+ DCs. Mechanistic analysis revealed a substantial reduction of two factors previously shown to be protective in cGN: FoxP3+ Tregs and IL-10. The latter was mainly produced by intrarenal Tregs but also, to some extent, by CD103+ DCs themselves. Systemic antirenal immune responses were unchanged in Batf3-deficient mice, validating a local effect by CD103+ DCs in the kidney rather than through Batf3–dependent CD8+ DCs in lymphatic tissues. This was corroborated by our results in Langerin-DTR mice, which allow for distinguishing between these two Batf3–dependent DC subsets.

The severity of cGN and Treg numbers in the three mouse lines examined here was tightly correlated with the efficiency and specificity of the CD103+ DC reduction. This was best in Batf3-deficient mice, and consistently, these mice showed the lowest Treg numbers and the most severe nephritis symptoms. In Langerin-DTR mice, specificity was equally high, but efficiency was moderate along with the effect on Tregs and cGN symptoms. DC reduction was better in Flt3L-deficient mice, but specificity for CD103+ DCs was not, so that some proinflammatory CD11b+ DCs were lost as well. Consistently, cGN was aggravated but not as severely as in Batf3-deficient mice. Thus, CD103+ renal DCs regulate the abundance of FoxP3+ Tregs in the kidney and thereby, regulate the progression of cGN.

In the intestine, lung, and skin, the ability of CD103+ DCs to induce Tregs has been documented, suggesting usefulness for the modulation of autoimmune diseases by harnessing their protective immunoregulatory functions.36,37,45,46 However, to our knowledge, our study is the first reporting aggravated inflammatory disease as a consequence. Several reports showed that Flt3−/− mice lack CD103+ DCs, and some of them documented fewer Tregs and more inflammation and tissue damage (for example, in the aorta), leading to exacerbated atherosclerosis.47 Furthermore, Flt3L supplementation expanded intestinal CD103+ DCs and increased Tregs, thereby attenuating murine inflammatory bowel disease.42 When we applied this approach in cGN, Flt3L also increased CD103+ DCs and Tregs in the kidney. Flt3L is known to increase not only CD103+ but also, CD11b+ tissue DC numbers to a lesser extent,20,23–25 and we found that this also applies to the kidney. However, CD11b+ DCs are 10 times more numerous in the kidney, so that a small relative increase raises absolute cell numbers as much as the great increase of the scarcer CD103+ DCs. This is different in intestine and lung, where CD11b+ DCs and CD103+ DCs are similarly frequent, so that Flt3L caused a comparatively stronger increase of CD103+ DCs.

The concomitant increase of both kidney DCs types might have balanced their anti- and proinflammatory effects, and cGN was unchanged. This unexpected hurdle was overcome by preventing the accumulation of proinflammatory CD11b+ DCs using CCR2-depleting antibodies, so that cGN was attenuated. It is unclear whether this approach is feasible in the human situation, but nevertheless, these findings show that increasing CD103+ DCs but not CD11b+ DCs increases intrarenal Treg numbers, supporting causality between these cell types.

We found two hypothetic mechanisms by which CD103+ renal DCs might sustain Tregs. First, in coculture experiments, only these DCs but not CD11b+ kidney DCs induced FoxP3+ Tregs ex vivo. This is consistent with previous studies showing that intestinal CD103+ DCs can drive Treg differentiation after migrating to mesenteric lymph nodes when retinoid acid and TGFβ are present.45,46 It remains to be seen whether these factors are also required by CD103+ kidney DCs, but it is likely that Treg induction takes place in the renal lymph nodes given that naive T cells hardly enter nonlymphoid tissues. Second, another hypothetic mechanism is the production of CCL20, the only ligand of CCR6, which is required for recruiting Tregs into the inflamed brain48,49 and kidney.50 In encephalitis, CCR6 also impaired the recruitment of pathogenic Th17 cells, so that disease severity was not substantially altered.48,49 Th17 cells also play a role in cGN,51,52 but the effect of CCR6 on Tregs prevailed, so that kidneys of CCR6-deficient mice contained fewer Tregs and more severe cGN was noted.15 This phenotype is very similar to what we observed in nephritic Batf3−/− mice. Moreover, CCL20 production was abrogated when CD103+ DCs were lacking. These findings suggest that CD103+ renal DCs regulate Treg numbers by promoting their differentiation and/or recruiting them into nephritic kidneys, but future studies are required to validate these hypotheses.

During glomerular inflammation, FoxP3+ Tregs are essential for the regulation of Th1 immune responses,11–13 and IL-10 is a major mechanism by which they do so.14 In line with diminished Treg numbers, we observed a profound reduction of IL-10 in kidneys of nephritic Batf3−/− compared with WT mice, and FoxP3+ Tregs, indeed, were a major source of this cytokine. However, also, CD103+ DCs produced some IL-10 and may, thus, potentially attenuate nephritis directly. This would explain previous studies showing a large proportion of IL-10+ immune cells other than Tregs in the kidney.14,53 It is also consistent with the particularly strong IL-10 production by kidney DCs at late stages of cGN7 when CD103+ DCs are especially numerous. However, the superior IL-10 production by Tregs will hamper the formal experimental proof that CD103+ DC–derived IL-10 is protective.

CD103+ DCs can play a proinflammatory role under infections conditions (for example, by activating antiviral CD8+ T cell responses through crosspresentation).30,54 Our results document an anti-inflammatory function in sterile inflammation. This may help explain why the deletion of all CD11c+ DCs aggravated some models of kidney inflammation9,55 but attenuated others.3,5,7 It is possible that, in these studies, either protective CD103+ DCs or harmful CD11b+ DCs were operative.

In summary, we showed that CD103+ kidney DCs are protective in cGN and antagonize the proinflammatory functions of CX3CR1–dependent CD11b+ kidney DCs. These findings identify a major role of a minor DC subset in immune-mediated GN. Strategies to improve the functions of CD103+ DCs might be of therapeutic use in this disease and potentially, in other inflammatory diseases.

Concise Methods

Mice, Reagents, and cGN Model

We bred 8- to 12-week-old C57BL/6, Batf3−/−, Flt3L−/−, Langerin-DTR, Foxp3IRES-mRFP × IL-10 ires gfp–enhanced reporter, and DO11.10 × DEREG mice and kept them under specific pathogen–free conditions at the animal facility of the University Clinic Bonn. cGN was induced by intraperitoneal (ip) injection of 0.35–0.45 ml nephritis serum per mouse as previously described.9,56 CD103+ DCs were depleted in Langerin-DTR mice by ip injection of 8 ng DT per 1 g body wt.57 DO11.10 × DEREG mice were treated with 40 ng/g mouse DT ip to deplete Foxp3+ Tregs.58 Reagents were from Sigma-Aldrich (St. Louis, MO ) if not specified otherwise. All animal studies have been approved by a Governmental Review Board (Landesamt für Natur, Umwelt und Verbraucherschutz, Recklinghausen, Germany); 5×105 B16 melanoma cells expressing either OVA or Flt3L59,60 were implanted subcutaneously Inflammatory DCs were depleted using 20μg of MC-21 per mouse per day, for five days. MC-21 was described as an depleting anti-CCR2 antibody.43

Histology

Light microscopy was performed on 3- to 5-μm paraffin sections of paraformaldehyde-fixed tissue stained by periodic acid–Schiff or Gömöri Methamine silver according to standard protocols. Kidney damage was histologically determined and documented by a nephropathologist blinded to the experimental groups.

Isolation of DCs from Murine Kidneys

Kidneys were digested with collagenase (Roche Diagnostics, Indianapolis, IN) and DNAse-I as described previously.2 Tubular fragments were removed by filtration. CD11b+ DCs or CD103+ DCs from kidneys were sorted with a BDAria Sorter (Becton Dickinson, San Diego, CA). Purity was usually 90%–95%.

Flow Cytometry

After treatment with Fc-blocking antibodies (Privigen; CLS Behring GmbH), cells were stained for 20 minutes at 4°C with fluorochrome-labeled mAbs against CD45 (clone 30-F11), CD11c (HL3), I-Ab (AF6–120.1), CD11b (M1/70), CD103 (2E7), F4/80 (BM8), Ly6G (1A8), CD4 (GK1.5), TCRβ (H57–597), CD25 (pC61), and FoxP3 (FJK-16s). All antibodies were from BioLegend (San Diego, CA) if not indicated otherwise. Absolute cell numbers were determined with Calibrite APC Beads (BD Biosciences, San Jose, CA), and cells were analyzed with a BDCanto II (Becton Dickinson).

Cytokine Measurement

Cytokines in kidney supernatants were determined by Flowcytometry Bead Assay (eBioscience, San Diego, CA) according to the manufacturer’s instructions. For cell type–specific measurements, single-cell suspensions were incubated in RPMI (10% FCS; Gibco, Carlsbad, CA) with 1 μl/ml GolgiPlug (BD Biosciences) for 4 hours at 37°C. After cell surface staining, cells were fixed in 2% paraformaldehyde for 10 minutes on ice and permeabilized with PBS containing 2% BSA and 0.5% Saponin for 20 minutes at room temperature. Intracellular staining was performed in that buffer for 20 minutes at room temperature using fluorochrome-labeled mAbs against TNFα (clone MP6-XT22), IL-6 (MP5–20F3), and IFNγ (XMG1.2; BD Biosciences). CCL20 was measured by ELISA (Bio-Techne).

In Vitro Treg Induction

NTS-treated mice were injected with 700 μg OVA 1 hour before DC isolation; 2×104 sorted kidney DCs were cocultured with 4×104 naïve Th cells in 200 μl RPMI medium (10% FCS; Gibco) in 96-well plates for 6 days. Naïve Th cells were obtained by sorting CD4+CD25−GFP– T cells from spleens of DT–treated DO11.10 × DEREG mice with an Aria Sorter (Becton Dickinson). Purity was usually about 95%. Because DO11.10 cells are H2-Kd restricted, we used C57BL/6 × Balb/c F1 mice as DC donors, ensuring that DO11.10 cells can recognize antigen. As a positive control for Treg generation, we coated wells with αCD3 (1 μg/ml) and added sorted T cells, αCD28 (2 μg/ml; BD Biosciences), TGFβ (5 ng/ml; Peprotech), and IL-2 (100 U/ml; Proleukin; Novartis, Basel, Switzerland).

RNA Preparation and RT-PCR

Whole-tissue RNA was extracted using the RNA NucleoSpin Kit (Macherey-Nagel) according to the manufacturer’s instructions. RNA was reverse transcribed into cDNA using the High-Capacity Reverse Transcription Kit and amplified by 40 PCR cycles using SYBR Green (Applied Biosystems, Foster City, CA). The following primer sequences were used:

  • IL-10 (forward): 5′-CCAGTTTTACCTGGTAGAAGTGATG-3′;

  • IL-10 (reverse): 5′-TGTCTAGGTCCTGGAGTCCAGCAGACTC-3′;

  • TGFβ (forward): 5′-GCTCGCTTTGTACAACAGCACC-3′; and

  • TGFβ (reverse): 5′-GCGGTCCACCATTAGCACG-3′.

All samples were run in triplicate and normalized to GAPDH.

Miscellaneous Assays

For the analysis of albumin excretion and creatinine clearance, urine was collected over 18 hours using metabolic cages. Albumin concentrations in the urine were measured using a commercial mouse albumin ELISA kit according to the manufacturer’s instructions (Bethyl Laboratories, Inc., Montgomery, TX). Serum and urine creatinine concentrations were analyzed in the central laboratory of the University Hospital of Bonn. Serum levels of murine IgG1 and IgG2a specific for sheep Ig were determined by ELISA (Bethyl Laboratories, Inc.).

Statistical Analyses

Results are expressed as means±SEMs. Comparisons were drawn using a two–tailed unpaired t, Kruskal–Wallis, or two–sided nonparametric Mann–Whitney U test as indicated. P values <0.05 were considered significant.

Disclosures

None.

Acknowledgments

We thank Magdalena Esser for excellent technical assistance, Ken Murphy for Batf3−/− mice, Tim Sparwasser for DEREG mice, and Björn Clausen for Langerin–diphtheria toxin receptor mice.

This work was supported by Bonfor (to B.D.G.E.); projects 4, 1, and 5 of Deutsche Forschungsgemeinschaft (DFG) KFO228 (to G.T., U.P., and C.K., respectively); the SFBTR57, the SFB1192; DFG grant BO 3755/2-1 (to P.B.); and German Federal Ministry of Education and Research grant BMBF 01GM1518A (to P.B.). C.K. is a member of the ExcellenceCluster ImmunoSensation. We acknowledge support from the Flow Cytometry Core Facility and the House for Experimental Therapy.

Footnotes

References

  1. ↵
    1. Soos TJ,
    2. Sims TN,
    3. Barisoni L,
    4. Lin K,
    5. Littman DR,
    6. Dustin ML,
    7. Nelson PJ
    : CX3CR1+ interstitial dendritic cells form a contiguous network throughout the entire kidney. Kidney Int 70: 591–596, 2006pmid:16760907
    OpenUrlCrossRefPubMed
  2. ↵
    1. Krüger T,
    2. Benke D,
    3. Eitner F,
    4. Lang A,
    5. Wirtz M,
    6. Hamilton-Williams EE,
    7. Engel D,
    8. Giese B,
    9. Müller-Newen G,
    10. Floege J,
    11. Kurts C
    : Identification and functional characterization of dendritic cells in the healthy murine kidney and in experimental glomerulonephritis. J Am Soc Nephrol 15: 613–621, 2004pmid:14978163
    OpenUrlAbstract/FREE Full Text
  3. ↵
    1. Dong X,
    2. Swaminathan S,
    3. Bachman LA,
    4. Croatt AJ,
    5. Nath KA,
    6. Griffin MD
    : Resident dendritic cells are the predominant TNF-secreting cell in early renal ischemia-reperfusion injury. Kidney Int 71: 619–628, 2007pmid:17311071
    OpenUrlCrossRefPubMed
  4. ↵
    1. Tittel AP,
    2. Heuser C,
    3. Ohliger C,
    4. Knolle PA,
    5. Engel DR,
    6. Kurts C
    : Kidney dendritic cells induce innate immunity against bacterial pyelonephritis. J Am Soc Nephrol 22: 1435–1441, 2011pmid:21757770
    OpenUrlAbstract/FREE Full Text
  5. ↵
    1. Mulay SR,
    2. Kulkarni OP,
    3. Rupanagudi KV,
    4. Migliorini A,
    5. Darisipudi MN,
    6. Vilaysane A,
    7. Muruve D,
    8. Shi Y,
    9. Munro F,
    10. Liapis H,
    11. Anders HJ
    : Calcium oxalate crystals induce renal inflammation by NLRP3-mediated IL-1β secretion. J Clin Invest 123: 236–246, 2013pmid:23221343
    OpenUrlCrossRefPubMed
  6. ↵
    1. Dong X,
    2. Bachman LA,
    3. Miller MN,
    4. Nath KA,
    5. Griffin MD
    : Dendritic cells facilitate accumulation of IL-17 T cells in the kidney following acute renal obstruction. Kidney Int 74: 1294–1309, 2008pmid:18974760
    OpenUrlCrossRefPubMed
  7. ↵
    1. Hochheiser K,
    2. Engel DR,
    3. Hammerich L,
    4. Heymann F,
    5. Knolle PA,
    6. Panzer U,
    7. Kurts C
    : Kidney dendritic cells become pathogenic during crescentic glomerulonephritis with proteinuria. J Am Soc Nephrol 22: 306–316, 2011pmid:21164025
    OpenUrlAbstract/FREE Full Text
  8. ↵
    1. Pindjakova J,
    2. Hanley SA,
    3. Duffy MM,
    4. Sutton CE,
    5. Weidhofer GA,
    6. Miller MN,
    7. Nath KA,
    8. Mills KH,
    9. Ceredig R,
    10. Griffin MD
    : Interleukin-1 accounts for intrarenal Th17 cell activation during ureteral obstruction. Kidney Int 81: 379–390, 2012pmid:21975862
    OpenUrlCrossRefPubMed
  9. ↵
    1. Scholz J,
    2. Lukacs-Kornek V,
    3. Engel DR,
    4. Specht S,
    5. Kiss E,
    6. Eitner F,
    7. Floege J,
    8. Groene HJ,
    9. Kurts C
    : Renal dendritic cells stimulate IL-10 production and attenuate nephrotoxic nephritis. J Am Soc Nephrol 19: 527–537, 2008pmid:18235094
    OpenUrlAbstract/FREE Full Text
  10. ↵
    1. Riedel JH,
    2. Paust HJ,
    3. Turner JE,
    4. Tittel AP,
    5. Krebs C,
    6. Disteldorf E,
    7. Wegscheid C,
    8. Tiegs G,
    9. Velden J,
    10. Mittrücker HW,
    11. Garbi N,
    12. Stahl RA,
    13. Steinmetz OM,
    14. Kurts C,
    15. Panzer U
    : Immature renal dendritic cells recruit regulatory CXCR6(+) invariant natural killer T cells to attenuate crescentic GN. J Am Soc Nephrol 23: 1987–2000, 2012pmid:23138484
    OpenUrlAbstract/FREE Full Text
  11. ↵
    1. Wolf D,
    2. Hochegger K,
    3. Wolf AM,
    4. Rumpold HF,
    5. Gastl G,
    6. Tilg H,
    7. Mayer G,
    8. Gunsilius E,
    9. Rosenkranz AR
    : CD4+CD25+ regulatory T cells inhibit experimental anti-glomerular basement membrane glomerulonephritis in mice. J Am Soc Nephrol 16: 1360–1370, 2005pmid:15788479
    OpenUrlAbstract/FREE Full Text
    1. Paust HJ,
    2. Ostmann A,
    3. Erhardt A,
    4. Turner JE,
    5. Velden J,
    6. Mittrücker HW,
    7. Sparwasser T,
    8. Panzer U,
    9. Tiegs G
    : Regulatory T cells control the Th1 immune response in murine crescentic glomerulonephritis. Kidney Int 80: 154–164, 2011pmid:21525855
    OpenUrlCrossRefPubMed
  13. ↵
    1. Ooi JD,
    2. Snelgrove SL,
    3. Engel DR,
    4. Hochheiser K,
    5. Ludwig-Portugall I,
    6. Nozaki Y,
    7. O’Sullivan KM,
    8. Hickey MJ,
    9. Holdsworth SR,
    10. Kurts C,
    11. Kitching AR
    : Endogenous foxp3(+) T-regulatory cells suppress anti-glomerular basement membrane nephritis. Kidney Int 79: 977–986, 2011pmid:21248715
    OpenUrlCrossRefPubMed
  14. ↵
    1. Ostmann A,
    2. Paust HJ,
    3. Panzer U,
    4. Wegscheid C,
    5. Kapffer S,
    6. Huber S,
    7. Flavell RA,
    8. Erhardt A,
    9. Tiegs G
    : Regulatory T cell-derived IL-10 ameliorates crescentic GN. J Am Soc Nephrol 24: 930–942, 2013pmid:23641052
    OpenUrlAbstract/FREE Full Text
  15. ↵
    1. Turner JE,
    2. Paust HJ,
    3. Steinmetz OM,
    4. Peters A,
    5. Riedel JH,
    6. Erhardt A,
    7. Wegscheid C,
    8. Velden J,
    9. Fehr S,
    10. Mittrücker HW,
    11. Tiegs G,
    12. Stahl RA,
    13. Panzer U
    : CCR6 recruits regulatory T cells and Th17 cells to the kidney in glomerulonephritis. J Am Soc Nephrol 21: 974–985, 2010pmid:20299360
    OpenUrlAbstract/FREE Full Text
  16. ↵
    1. Power CA,
    2. Church DJ,
    3. Meyer A,
    4. Alouani S,
    5. Proudfoot AE,
    6. Clark-Lewis I,
    7. Sozzani S,
    8. Mantovani A,
    9. Wells TN
    : Cloning and characterization of a specific receptor for the novel CC chemokine MIP-3alpha from lung dendritic cells. J Exp Med 186: 825–835, 1997pmid:9294137
    OpenUrlAbstract/FREE Full Text
  17. ↵
    1. Steinman RM,
    2. Idoyaga J
    : Features of the dendritic cell lineage. Immunol Rev 234: 5–17, 2010pmid:20193008
    OpenUrlCrossRefPubMed
  18. ↵
    1. Geissmann F,
    2. Manz MG,
    3. Jung S,
    4. Sieweke MH,
    5. Merad M,
    6. Ley K
    : Development of monocytes, macrophages, and dendritic cells. Science 327: 656–661, 2010pmid:20133564
    OpenUrlAbstract/FREE Full Text
  19. ↵
    1. Nelson PJ,
    2. Rees AJ,
    3. Griffin MD,
    4. Hughes J,
    5. Kurts C,
    6. Duffield J
    : The renal mononuclear phagocytic system. J Am Soc Nephrol 23: 194–203, 2012pmid:22135312
    OpenUrlAbstract/FREE Full Text
  20. ↵
    1. Ginhoux F,
    2. Liu K,
    3. Helft J,
    4. Bogunovic M,
    5. Greter M,
    6. Hashimoto D,
    7. Price J,
    8. Yin N,
    9. Bromberg J,
    10. Lira SA,
    11. Stanley ER,
    12. Nussenzweig M,
    13. Merad M
    : The origin and development of nonlymphoid tissue CD103+ DCs. J Exp Med 206: 3115–3130, 2009pmid:20008528
    OpenUrlAbstract/FREE Full Text
    1. Guilliams M,
    2. Henri S,
    3. Tamoutounour S,
    4. Ardouin L,
    5. Schwartz-Cornil I,
    6. Dalod M,
    7. Malissen B
    : From skin dendritic cells to a simplified classification of human and mouse dendritic cell subsets. Eur J Immunol 40: 2089–2094, 2010pmid:20853491
    OpenUrlCrossRefPubMed
  22. ↵
    1. Merad M,
    2. Sathe P,
    3. Helft J,
    4. Miller J,
    5. Mortha A
    : The dendritic cell lineage: Ontogeny and function of dendritic cells and their subsets in the steady state and the inflamed setting. Annu Rev Immunol 31: 563–604, 2013pmid:23516985
    OpenUrlCrossRefPubMed
  23. ↵
    1. Burkly L,
    2. Hession C,
    3. Ogata L,
    4. Reilly C,
    5. Marconi LA,
    6. Olson D,
    7. Tizard R,
    8. Cate R,
    9. Lo D
    : Expression of relB is required for the development of thymic medulla and dendritic cells. Nature 373: 531–536, 1995pmid:7845467
    OpenUrlCrossRefPubMed
    1. Maraskovsky E,
    2. Brasel K,
    3. Teepe M,
    4. Roux ER,
    5. Lyman SD,
    6. Shortman K,
    7. McKenna HJ
    : Dramatic increase in the numbers of functionally mature dendritic cells in Flt3 ligand-treated mice: Multiple dendritic cell subpopulations identified. J Exp Med 184: 1953–1962, 1996pmid:8920882
    OpenUrlAbstract/FREE Full Text
  25. ↵
    1. McKenna HJ,
    2. Stocking KL,
    3. Miller RE,
    4. Brasel K,
    5. De Smedt T,
    6. Maraskovsky E,
    7. Maliszewski CR,
    8. Lynch DH,
    9. Smith J,
    10. Pulendran B,
    11. Roux ER,
    12. Teepe M,
    13. Lyman SD,
    14. Peschon JJ
    : Mice lacking flt3 ligand have deficient hematopoiesis affecting hematopoietic progenitor cells, dendritic cells, and natural killer cells. Blood 95: 3489–3497, 2000pmid:10828034
    OpenUrlAbstract/FREE Full Text
  26. ↵
    1. Hildner K,
    2. Edelson BT,
    3. Purtha WE,
    4. Diamond M,
    5. Matsushita H,
    6. Kohyama M,
    7. Calderon B,
    8. Schraml BU,
    9. Unanue ER,
    10. Diamond MS,
    11. Schreiber RD,
    12. Murphy TL,
    13. Murphy KM
    : Batf3 deficiency reveals a critical role for CD8alpha+ dendritic cells in cytotoxic T cell immunity. Science 322: 1097–1100, 2008pmid:19008445
    OpenUrlAbstract/FREE Full Text
  27. ↵
    1. Shortman K,
    2. Heath WR
    : The CD8+ dendritic cell subset. Immunol Rev 234: 18–31, 2010pmid:20193009
    OpenUrlCrossRefPubMed
  28. ↵
    1. Mashayekhi M,
    2. Sandau MM,
    3. Dunay IR,
    4. Frickel EM,
    5. Khan A,
    6. Goldszmid RS,
    7. Sher A,
    8. Ploegh HL,
    9. Murphy TL,
    10. Sibley LD,
    11. Murphy KM
    : CD8α(+) dendritic cells are the critical source of interleukin-12 that controls acute infection by Toxoplasma gondii tachyzoites. Immunity 35: 249–259, 2011pmid:21867928
    OpenUrlCrossRefPubMed
  29. ↵
    1. den Haan JM,
    2. Lehar SM,
    3. Bevan MJ
    : CD8(+) but not CD8(-) dendritic cells cross-prime cytotoxic T cells in vivo. J Exp Med 192: 1685–1696, 2000pmid:11120766
    OpenUrlAbstract/FREE Full Text
  30. ↵
    1. del Rio ML,
    2. Rodriguez-Barbosa JI,
    3. Kremmer E,
    4. Förster R
    : CD103- and CD103+ bronchial lymph node dendritic cells are specialized in presenting and cross-presenting innocuous antigen to CD4+ and CD8+ T cells. J Immunol 178: 6861–6866, 2007pmid:17513734
    OpenUrlAbstract/FREE Full Text
  31. ↵
    1. Gottschalk C,
    2. Damuzzo V,
    3. Gotot J,
    4. Kroczek RA,
    5. Yagita H,
    6. Murphy KM,
    7. Knolle PA,
    8. Ludwig-Portugall I,
    9. Kurts C
    : Batf3-dependent dendritic cells in the renal lymph node induce tolerance against circulating antigens. J Am Soc Nephrol 24: 543–549, 2013pmid:23411785
    OpenUrlAbstract/FREE Full Text
  32. ↵
    1. Kurts C,
    2. Robinson BW,
    3. Knolle PA
    : Cross-priming in health and disease. Nat Rev Immunol 10: 403–414, 2010pmid:20498667
    OpenUrlCrossRefPubMed
  33. ↵
    1. Wang Y,
    2. Wang YP,
    3. Tay YC,
    4. Harris DC
    : Role of CD8(+) cells in the progression of murine adriamycin nephropathy. Kidney Int 59: 941–949, 2001pmid:11231349
    OpenUrlCrossRefPubMed
  34. ↵
    1. Schulz O,
    2. Jaensson E,
    3. Persson EK,
    4. Liu X,
    5. Worbs T,
    6. Agace WW,
    7. Pabst O
    : Intestinal CD103+, but not CX3CR1+, antigen sampling cells migrate in lymph and serve classical dendritic cell functions. J Exp Med 206: 3101–3114, 2009pmid:20008524
    OpenUrlAbstract/FREE Full Text
  35. ↵
    1. Denning TL,
    2. Wang YC,
    3. Patel SR,
    4. Williams IR,
    5. Pulendran B
    : Lamina propria macrophages and dendritic cells differentially induce regulatory and interleukin 17-producing T cell responses. Nat Immunol 8: 1086–1094, 2007pmid:17873879
    OpenUrlCrossRefPubMed
  36. ↵
    1. Coombes JL,
    2. Siddiqui KR,
    3. Arancibia-Cárcamo CV,
    4. Hall J,
    5. Sun CM,
    6. Belkaid Y,
    7. Powrie F
    : A functionally specialized population of mucosal CD103+ DCs induces Foxp3+ regulatory T cells via a TGF-beta and retinoic acid-dependent mechanism. J Exp Med 204: 1757–1764, 2007pmid:17620361
    OpenUrlAbstract/FREE Full Text
  37. ↵
    1. Sun CM,
    2. Hall JA,
    3. Blank RB,
    4. Bouladoux N,
    5. Oukka M,
    6. Mora JR,
    7. Belkaid Y
    : Small intestine lamina propria dendritic cells promote de novo generation of Foxp3 T reg cells via retinoic acid. J Exp Med 204: 1775–1785, 2007pmid:17620362
    OpenUrlAbstract/FREE Full Text
  38. ↵
    1. Scott CL,
    2. Aumeunier AM,
    3. Mowat AM
    : Intestinal CD103+ dendritic cells: Master regulators of tolerance? Trends Immunol 32: 412–419, 2011pmid:21816673
    OpenUrlCrossRefPubMed
  39. ↵
    1. Edelson BT,
    2. Kc W,
    3. Juang R,
    4. Kohyama M,
    5. Benoit LA,
    6. Klekotka PA,
    7. Moon C,
    8. Albring JC,
    9. Ise W,
    10. Michael DG,
    11. Bhattacharya D,
    12. Stappenbeck TS,
    13. Holtzman MJ,
    14. Sung SS,
    15. Murphy TL,
    16. Hildner K,
    17. Murphy KM
    : Peripheral CD103+ dendritic cells form a unified subset developmentally related to CD8alpha+ conventional dendritic cells. J Exp Med 207: 823–836, 2010pmid:20351058
    OpenUrlAbstract/FREE Full Text
  40. ↵
    1. Hochheiser K,
    2. Heuser C,
    3. Krause TA,
    4. Teteris S,
    5. Ilias A,
    6. Weisheit C,
    7. Hoss F,
    8. Tittel AP,
    9. Knolle PA,
    10. Panzer U,
    11. Engel DR,
    12. Tharaux PL,
    13. Kurts C
    : Exclusive CX3CR1 dependence of kidney DCs impacts glomerulonephritis progression. J Clin Invest 123: 4242–4254, 2013pmid:23999431
    OpenUrlCrossRefPubMed
  41. ↵
    1. Waskow C,
    2. Liu K,
    3. Darrasse-Jèze G,
    4. Guermonprez P,
    5. Ginhoux F,
    6. Merad M,
    7. Shengelia T,
    8. Yao K,
    9. Nussenzweig M
    : The receptor tyrosine kinase Flt3 is required for dendritic cell development in peripheral lymphoid tissues. Nat Immunol 9: 676–683, 2008pmid:18469816
    OpenUrlCrossRefPubMed
  42. ↵
    1. Collins CB,
    2. Aherne CM,
    3. McNamee EN,
    4. Lebsack MDP,
    5. Eltzschig H,
    6. Jedlicka P,
    7. Rivera-Nieves J
    : Flt3 ligand expands CD103⁺ dendritic cells and FoxP3⁺ T regulatory cells, and attenuates Crohn’s-like murine ileitis. Gut 61: 1154–1162, 2012pmid:22068168
    OpenUrlAbstract/FREE Full Text
  43. ↵
    Mack M, Cihak J, Simonis C, Luckow B, Proudfoot AE, Plachý J, Brühl H, Frink M, Anders HJ, Vielhauer V, Pfirstinger J, Stangassinger M, Schlöndorff D: Expression and characterization of the chemokine receptors CCR2 and CCR5 in mice. J Immunol 166: 4697–4704, 2001
  44. ↵
    1. Croce AC,
    2. Ferrigno A,
    3. Santin G,
    4. Vairetti M,
    5. Bottiroli G
    : Bilirubin: An autofluorescence bile biomarker for liver functionality monitoring. J Biophotonics 7: 810–817, 2014pmid:23616471
    OpenUrlCrossRefPubMed
  45. ↵
    1. Idoyaga J,
    2. Fiorese C,
    3. Zbytnuik L,
    4. Lubkin A,
    5. Miller J,
    6. Malissen B,
    7. Mucida D,
    8. Merad M,
    9. Steinman RM
    : Specialized role of migratory dendritic cells in peripheral tolerance induction. J Clin Invest 123: 844–854, 2013pmid:23298832
    OpenUrlPubMed
  46. ↵
    1. Khare A,
    2. Krishnamoorthy N,
    3. Oriss TB,
    4. Fei M,
    5. Ray P,
    6. Ray A
    : Cutting edge: Inhaled antigen upregulates retinaldehyde dehydrogenase in lung CD103+ but not plasmacytoid dendritic cells to induce Foxp3 de novo in CD4+ T cells and promote airway tolerance. J Immunol 191: 25–29, 2013pmid:23733880
    OpenUrlAbstract/FREE Full Text
  47. ↵
    1. Choi J-H,
    2. Cheong C,
    3. Dandamudi DB,
    4. Park CG,
    5. Rodriguez A,
    6. Mehandru S,
    7. Velinzon K,
    8. Jung I-H,
    9. Yoo J-Y,
    10. Oh GT,
    11. Steinman RM
    : Flt3 signaling-dependent dendritic cells protect against atherosclerosis. Immunity 35: 819–831, 2011pmid:22078798
    OpenUrlCrossRefPubMed
  48. ↵
    1. Villares R,
    2. Cadenas V,
    3. Lozano M,
    4. Almonacid L,
    5. Zaballos A,
    6. Martínez-A C,
    7. Varona R
    : CCR6 regulates EAE pathogenesis by controlling regulatory CD4+ T-cell recruitment to target tissues. Eur J Immunol 39: 1671–1681, 2009pmid:19499521
    OpenUrlCrossRefPubMed
  49. ↵
    1. Elhofy A,
    2. Depaolo RW,
    3. Lira SA,
    4. Lukacs NW,
    5. Karpus WJ
    : Mice deficient for CCR6 fail to control chronic experimental autoimmune encephalomyelitis. J Neuroimmunol 213: 91–99, 2009pmid:19535153
    OpenUrlCrossRefPubMed
  50. ↵
    1. Kurts C,
    2. Panzer U,
    3. Anders HJ,
    4. Rees AJ
    : The immune system and kidney disease: Basic concepts and clinical implications. Nat Rev Immunol 13: 738–753, 2013pmid:24037418
    OpenUrlCrossRefPubMed
  51. ↵
    1. Paust HJ,
    2. Turner JE,
    3. Steinmetz OM,
    4. Peters A,
    5. Heymann F,
    6. Hölscher C,
    7. Wolf G,
    8. Kurts C,
    9. Mittrücker HW,
    10. Stahl RA,
    11. Panzer U
    : The IL-23/Th17 axis contributes to renal injury in experimental glomerulonephritis. J Am Soc Nephrol 20: 969–979, 2009pmid:19339380
    OpenUrlAbstract/FREE Full Text
  52. ↵
    1. Summers SA,
    2. Steinmetz OM,
    3. Li M,
    4. Kausman JY,
    5. Semple T,
    6. Edgtton KL,
    7. Borza DB,
    8. Braley H,
    9. Holdsworth SR,
    10. Kitching AR
    : Th1 and Th17 cells induce proliferative glomerulonephritis. J Am Soc Nephrol 20: 2518–2524, 2009pmid:19820122
    OpenUrlAbstract/FREE Full Text
  53. ↵
    1. Reantragoon R,
    2. Corbett AJ,
    3. Sakala IG,
    4. Gherardin NA,
    5. Furness JB,
    6. Chen Z,
    7. Eckle SB,
    8. Uldrich AP,
    9. Birkinshaw RW,
    10. Patel O,
    11. Kostenko L,
    12. Meehan B,
    13. Kedzierska K,
    14. Liu L,
    15. Fairlie DP,
    16. Hansen TH,
    17. Godfrey DI,
    18. Rossjohn J,
    19. McCluskey J,
    20. Kjer-Nielsen L
    : Antigen-loaded MR1 tetramers define T cell receptor heterogeneity in mucosal-associated invariant T cells. J Exp Med 210: 2305–2320, 2013pmid:24101382
    OpenUrlAbstract/FREE Full Text
  54. ↵
    1. Bedoui S,
    2. Whitney PG,
    3. Waithman J,
    4. Eidsmo L,
    5. Wakim L,
    6. Caminschi I,
    7. Allan RS,
    8. Wojtasiak M,
    9. Shortman K,
    10. Carbone FR,
    11. Brooks AG,
    12. Heath WR
    : Cross-presentation of viral and self antigens by skin-derived CD103+ dendritic cells. Nat Immunol 10: 488–495, 2009pmid:19349986
    OpenUrlCrossRefPubMed
  55. ↵
    1. Tadagavadi RK,
    2. Reeves WB
    : Renal dendritic cells ameliorate nephrotoxic acute kidney injury. J Am Soc Nephrol 21: 53–63, 2010pmid:19875815
    OpenUrlAbstract/FREE Full Text
  56. ↵
    1. Gotot J,
    2. Piotrowski E,
    3. Otte MS,
    4. Tittel AP,
    5. Linlin G,
    6. Yao C,
    7. Ziegelbauer K,
    8. Panzer U,
    9. Garbi N,
    10. Kurts C,
    11. Thaiss F
    : Inhibitor of NFκB kinase subunit 2 blockade hinders the initiation but aggravates the progression of crescentic GN [published online ahead of print November 16, 2015]. J Am Soc Nephrol doi:ASN.2015060699pmid:26574045
    OpenUrlAbstract/FREE Full Text
  57. ↵
    1. Bennett CL,
    2. van Rijn E,
    3. Jung S,
    4. Inaba K,
    5. Steinman RM,
    6. Kapsenberg ML,
    7. Clausen BE
    : Inducible ablation of mouse Langerhans cells diminishes but fails to abrogate contact hypersensitivity. J Cell Biol 169: 569–576, 2005pmid:15897263
    OpenUrlAbstract/FREE Full Text
  58. ↵
    1. Lahl K,
    2. Loddenkemper C,
    3. Drouin C,
    4. Freyer J,
    5. Arnason J,
    6. Eberl G,
    7. Hamann A,
    8. Wagner H,
    9. Huehn J,
    10. Sparwasser T
    : Selective depletion of Foxp3+ regulatory T cells induces a scurfy-like disease. J Exp Med 204: 57–63, 2007pmid:17200412
    OpenUrlAbstract/FREE Full Text
  59. ↵
    1. Mach N,
    2. Gillessen S,
    3. Wilson SB,
    4. Sheehan C,
    5. Mihm M,
    6. Dranoff G
    : Differences in dendritic cells stimulated in vivo by tumors engineered to secrete granulocyte-macrophage colony-stimulating factor or Flt3-ligand. Cancer Res 60: 3239–3246, 2000pmid:10866317
    OpenUrlAbstract/FREE Full Text
  60. ↵
    1. Zou T,
    2. Caton AJ,
    3. Koretzky GA,
    4. Kambayashi T
    : Dendritic cells induce regulatory T cell proliferation through antigen-dependent and -independent interactions. J Immunol 185: 2790–2799, 2010pmid:20686126
    OpenUrlAbstract/FREE Full Text
View Abstract
Back to top

In this issue

View Selected Citations (0)
Print
Download PDF
Article Alerts
Email Article
Citation Tools
Request Permissions
CD103+ Kidney Dendritic Cells Protect against Crescentic GN by Maintaining IL-10–Producing Regulatory T Cells
Beatrix D.G. Evers, Daniel R. Engel, Alexander M.C. Böhner, André P. Tittel, Torsten A. Krause, Christoph Heuser, Natalio Garbi, Wolfgang Kastenmüller, Matthias Mack, Gisa Tiegs, Ulf Panzer, Peter Boor, Isis Ludwig-Portugall, Christian Kurts
JASN Nov 2016, 27 (11) 3368-3382; DOI: 10.1681/ASN.2015080873
del.icio.us logo Digg logo Reddit logo Twitter logo CiteULike logo Facebook logo Google logo Mendeley logo

Jump to section

Keywords