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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 August 1, 2018; First published July 9, 2018
Citation Information: J Clin Invest. 2018;128(8):3413-3424. https://doi.org/10.1172/JCI97879.
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Categories: 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 5

Effects of BC rupture on glomerular localization of CD68 macrophages.

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Effects of BC rupture on glomerular localization of CD68 macrophages.
(A...
(A) Representative immunostained images of CD68+ macrophages in glomeruli with intact versus ruptured BC. Ruptured BC is associated with an increase in CD68+ macrophages infiltrating the glomerular space (indicated by white arrows). Original magnification, ×400. (B) Quantification of intraglomerular CD68+ area for intact versus ruptured BC (n = 53 glomeruli for intact, n = 29 glomeruli for ruptured BC in NTS plus control T cell group; n = 51 glomeruli for intact, n = 48 ruptured BC in NTS plus Jedi T cell group). ****P < 0.0001, compared between indicated groups by paired t test.
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