1. Volume 82, Issue 1, Pages 60-71 (July 2012)
Characterization of the renal CD4+ T-cell response in experimental autoimmune glomerulonephritis 
Helmut Hopfer, Julia Holzer, Stefanie Hünemörder, Hans-Joachim Paust, Marlies Sachs, Catherine Meyer-Schwesinger, Jan-Eric Turner, Ulf Panzer, Hans-Willi Mittrücker 
Kidney International 
Volume 82, Issue 1, Pages (July 2012)
DOI: /ki
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2. Figure 1
Experimental autoimmune glomerulonephritis (EAG) in DBA/1 mice. (a) Time point of first clinical signs of EAG according to a stress score (α3IV-NC1-immunized vs. mock-immunized mice: P<0.001). (b) Albumin in urine normalized to creatinine (maximum of detection 1000 (g/g)). (c) Blood urea nitrogen (BUN) from mice analyzed at 8 and 10 weeks post immunization as well as from EAG mice (control vs. EAG, P<0.01). (d) Crescent count on periodic acid–Schiff-stained paraffin sections (control and weeks 3, 5, 7, and 8 vs. EAG: P<0.05). (e) Assessment of tubulointerstitial (tub-int) damage using a semiquantitative score (control and weeks 3, 5, 7, and 8 vs. EAG: P<0.05). (f) Linear regression analysis of crescent formation vs. time point of sacrifice (r2=0.0561, P=NS (not significant)) (b–f: each symbol represents data of an individual mouse; the bar gives the median).
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3. Figure 2
Histological findings in experimental autoimmune glomerulonephritis (EAG) mice. (a–d) Medium and high power magnifications of crescentic glomerulonephritis accompanied by tubulointerstitial damage in EAG mice (b, d) and normal kidney histology in control mice (a, c). (e) Focal pulmonary necrosis in some EAG mice. (f) Immunoglobulin (Ig)G deposition along the glomerular basement membranes (GBMs) in EAG mice. Note segmental GBM ruptures. (g, h) Immunohistochemistry revealing F4/80+ macrophages cells in EAG (h), but not control kidneys (g). (i, j) Immunohistochemistry showing infiltration of the kidney by CD3+ T cells in EAG (j) and control mice (i). (a–d: periodic acid–Schiff stain, original magnification × 100 or × 600; e: hematoxylin and eosin stain, original magnification × 200; f–j: immunohistochemistry of paraffin section, original magnification × 600 or × 400.)
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4. Figure 3
α3IV-NC1-specific serum antibodies, glomerular immunoglobulin (Ig)G and C3 deposition, and circulating immune complexes (IC). (a) Indirect enzyme-linked immunosorbent assay (ELISA) of human (h) α3IV-NC1-specific IgG in serum, P<0.005 for all time points. (b) Crossreactivity of α3IV-NC1-specific IgG to mouse (m) α3IV-NC1, P< (c) Semiquantitative evaluation of IgG immunofluorescence to assess glomerular IgG deposition. (d) Representative pictures of glomerular IgG deposition from mice analyzed at 3, 5, and 7 weeks and from experimental autoimmune glomerulonephritis (EAG) mice. Note granular glomerular basement membrane (GBM) staining (inset). (e) Representative pictures of glomerular C3 deposition. (f) Semiquantitative scoring of C3 immunofluorescence. (g) ELISA specific for circulating IC (IgM, IgG, and IgA) in mouse serum, P=NS. a, b, and g: Each circle represents data of an individual mouse; the bar gives the median. c, f: For each time point kidneys from 4–10 mice were analyzed. Bars show the mean and standard deviation of % glomeruli in the four categories. d, e: Direct immunofluorescence of cryo sections, original magnification × 400.
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5. Figure 4
Renal macrophages in experimental autoimmune glomerulonephritis (EAG). (a) Quantification of immunohistochemical MAC2 staining expressed as number of MAC2+ cells per 100 glomerular cross sections (P<0.01). (b) Morphometry of F4/80 immunohistochemistry (P<0005). (c) Fluorescence-activated cell sorting (FACS) analysis of renal cells. Cells were characterized for CD45, CD11b, F4/80, and Gr-1 expression. Blots show CD45+ CD11bhigh cells of tissues from individual mice. Numbers give %-values for macrophages (F4/80+ Gr-1low) and granulocytes (F4/80low Gr-1high) calculated for myeloid cells (CD11b+ CD45+). (d) Distribution of macrophages (CD11b+ F4/80+ Gr-1low) in relation to CD45+ leukocytes (left panel; naïve, week 3, and week 5 vs. EAG P<0.05 for macrophages in the kidney) or in relation to all acquired events (right panel: all time points vs. EAG P<0.01 for macrophages in the kidney) (c: representative dot blots; a, b, d: symbols represent data from individually analyzed mice; the bar gives the median).
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6. Figure 5
Renal T cells in experimental autoimmune glomerulonephritis (EAG). (a) Quantification of immunohistochemical CD3 staining expressed as number of CD3+ cells per mm2 renal cortex (control and week 10 vs. EAG P<0.05) or (b) per 100 glomerular cross sections (P=NS (not significant)). (c) Fluorescence-activated cell sorting analysis of renal T cells. Frequencies of renal CD4+ (left panel) and CD8+ T cells (right panel) are given in relation to all acquired events. (d) Relative intrarenal mRNA expression of chemokines and chemokine receptors by real time reverse-transcriptase–PCR (for all panels: control vs. EAG P<0.05). (a–d: each circle represents data of an individual mouse; the bar gives the median.)
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7. Figure 6
Phenotypical and functional analysis of renal T cells. (a) Activation status of renal CD4+ T cells. Blots show CD44 and CD62L expression for CD4+ CD11blow CD45+ cells. Numbers give the %-values for naive (CD62L+ CD44low) and effector or effector memory T cells (CD62L− CD44high). (b) Intracellular staining of interferon (IFN)γ and interleukin (IL)-17A in CD4+ T cells after polyclonal in vitro stimulation with phorbol 12-myristate 13-acetate (PMA)+ionomycin (iono). (c) Evaluation of IFNγ and IL-17A production of CD4+ T cells after incubation after stimulation with PMA + iono. Data are presented as Δ-cytokine values, which is %-value of positive cells after stimulation minus the %-values of cells without stimulation (kidney naïve vs. experimental autoimmune glomerulonephritis (EAG): IFNγ P<0.05, IL-17A P<0.01). (d) Relative intrarenal mRNA expression of IFNγ and IL-17A by real time reverse-transcriptase–PCR (both panels: control vs. EAG P<0.05). (a, b: blots show representative results for tissues of individually analyzed mice; c, d: each circles represents data of an individual mouse; the bar gives the median.)
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8. Figure 7
Detection of α3IV-NC1-specific interferon (IFN)γ producing renal T cells. (a) Representative flow cytometric analysis of renal T cells isolated from experimental autoimmune glomerulonephritis (EAG) and control kidneys and of splenocytes used as antigen presenting cells (APCs). Renal cells were gated for CD45+ CD3+ cells. Plots show the percentage of positive cells. (b) IFNγ Elispot of isolated renal cells restimulated in vitro in the presence of APCs. Renal cells (RC) from EAG kidneys (EAG CD90+ RC) or control kidneys (Control CD90+ RC) were stimulated with α3IV-NC1 (α3), no antigen (no), or irrelevant antigens α1IV- (open circles) or α2IV-NC1 (closed circles). Data are presented as ΔIFNγ spots, which is the number of IFNγ spots in renal cells mixed with APCs minus the number of background IFNγ spots in APCs alone. (b: each circle represents data of an individual mouse; the bar gives the median.) FACS, fluorescence-activated cell sorting; FITC, fluorescein isothiocyanate; MACS, magnetic cell separation; MHC, major histocompatibility complex; NS, not significant; PE, phycoerythrine.
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