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Bowman’s capsule provides a protective niche for podocytes from cytotoxic CD8+ T cells
Anqun Chen, … , Detlef Schlondorff, Judith Agudo
Anqun Chen, … , Detlef Schlondorff, Judith Agudo
Published July 9, 2018
Citation Information: J Clin Invest. 2018;128(8):3413-3424. https://doi.org/10.1172/JCI97879.
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Concise Communication Immunology Nephrology

Bowman’s capsule provides a protective niche for podocytes from cytotoxic CD8+ T cells

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Abstract

T cells play a key role in immune-mediated glomerulonephritis, but how cytotoxic T cells interact with podocytes remains unclear. To address this, we injected EGFP-specific CD8+ T cells from just EGFP death inducing (Jedi) mice into transgenic mice with podocyte-specific expression of EGFP. In healthy mice, Jedi T cells could not access EGFP+ podocytes. Conversely, when we induced nephrotoxic serum nephritis (NTSN) and injected Jedi T cells, EGFP+ podocyte transgenic mice showed enhanced proteinuria and higher blood urea levels. Morphometric analysis showed greater loss of EGFP+ podocytes, which was associated with severe crescentic and necrotizing glomerulonephritis. Notably, only glomeruli with disrupted Bowman’s capsule displayed massive CD8+ T cell infiltrates that were in direct contact with EGFP+ podocytes, causing their apoptosis. Thus, under control conditions with intact Bowman’s capsule, podocytes are not accessible to CD8+ T cells. However, breaches in Bowman’s capsule, as also noted in human crescentic glomerulonephritis, allow access of CD8+ T cells to the glomerular tuft and podocytes, resulting in their destruction. Through these mechanisms, a potentially reversible glomerulonephritis undergoes an augmentation process to a rapidly progressive glomerulonephritis, leading to end-stage kidney disease. Translating these mechanistic insights to human crescentic nephritis should direct future therapeutic interventions at blocking CD8+ T cells, especially in progressive stages of rapidly progressive glomerulonephritis.

Authors

Anqun Chen, Kyung Lee, Vivette D. D’Agati, Chengguo Wei, Jia Fu, Tian-Jun Guan, John Cijiang He, Detlef Schlondorff, Judith Agudo

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Figure 3

Histopathological analysis of mouse kidneys.

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Histopathological analysis of mouse kidneys.
(A) Representative images o...
(A) Representative images of H&E- and PAS-stained kidneys from mice injected with NTS. Destruction of glomeruli with inflammatory infiltrates and apoptosis and massive pathological worsening with defects in BC are apparent in kidneys of NTS plus Jedi T cell–injected mice. BC rupture is indicated by black arrows in PAS images. Bottom panel shows the immunofluorescence of MHC-I in all groups. Original magnification, ×200 (top row); ×600 (second and third rows); ×400 (bottom row). (B) Quantification of histopathology from 90 to 170 glomeruli per kidney section for each mouse of the 4 to 6 mice per group. ***P < 0.001, compared with all other groups by ANOVA with Bonferroni’s correction for multiple comparisons.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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