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Updated: Jun 3, 2026

Glomerular Outgrowth as an Ex Vivo Assay to Analyze Pathways Involved in Parietal Epithelial Cell Activation
Published on: August 19, 2020
[Cellular components of crescents in four common types of crescentic glomerulonephritis]
Chen Wang1, Wan-zhong Zou, Xin Zheng
1Department of Nephrology, Peking University First Hospital, Peking University Institute of Nephrology, Beijing 100034, China.
Insights
Cellular crescents in glomerulonephritis involve proliferating parietal epithelial cells (PEC), macrophages, and podocytes. This cellular activity suggests these cells are key to crescent formation in various kidney diseases.
Area of Science:
- Nephrology
- Cell Biology
- Immunopathology
Context:
- Crescentic glomerulonephritis (CGN) is a severe kidney disease characterized by rapid glomerular injury.
- Understanding the cellular dynamics of crescent formation is crucial for developing targeted therapies.
Purpose:
- To investigate the cellular components involved in crescent formation across four major types of human CGN: anti-GBM disease (GBM-CGN), IgA nephropathy (IgA-CGN), ANCA-associated vasculitis (ANCA-CGN), and lupus nephritis (LN-CGN).
Summary:
- Immunohistochemistry revealed distinct cellular contributions to crescents, with parietal epithelial cells (PEC), macrophages, and podocytes playing significant roles.
- A notable difference in nestin and podocalyxin expression suggests podocyte dedifferentiation during crescentogenesis.
- Proliferating cells (PCNA-positive) were abundant and co-localized with PEC, macrophage, and podocyte markers, indicating active cellular proliferation.
Impact:
- Identifies key cellular players and processes, such as proliferation and dedifferentiation, in CGN crescent formation.
- Provides a basis for further research into the specific mechanisms driving crescent development in different CGN subtypes.
- May inform future therapeutic strategies aimed at modulating cellular behavior to prevent or treat crescentic kidney disease.
Objective:
To examine the cellular components at different stages of the crescent formation in four most common types of human crescentic glomerulonephritis (CGN), including anti-GBM disease (GBM-CGN), crescentic IgA nephropathy (IgA-CGN), ANCA associated pauci-immune CGN (ANCA-CGN) and crescentic lupus glomerulonephritis (LN-CGN).
Methods:
Renal biopsy specimens of patients with GBM-CGN (n = 10), IgA-CGN (n = 12), ANCA-CGN (n = 12), and LN-CGN (n = 11) were selected. Immunohistochemistry was adopted to identify the cellular components using different cell markers including cytokeratin (PEC), CD68 (macrophage), nestin (podocyte), podocalyxin (podocyte), CD3 (lymphocyte), CD15 (neutrophil) and PCNA.
Results:
There were different subtypes of cell components identified during the formation of a cellular crescent in 4 different types of human CGN. Mainly of PEC 11.4 (0.0, 95.0)%, macrophage 8.0 (0.0, 35.0)% and podocyte 5.5 (0.0, 22.0)% and their constitutive percentages were different among various CGNs (P < 0.01). In all the CGNs studied, there were 50% of cells were negative to all the cell markers adopted for this expeiment. Podocalyxin positive cells 0.5 (0.0, 9.6)% were significantly less than nestin positive cells 5.5 (0.0, 22.0)% in all CGNs. PCNA positive cells were 44.7 (16.7, 83.3)% in the cellular crescent of all CGNs and co-localized with nestin (38/45 cases), CK (42/45 cases) or CD68 (24/45 cases).
Conclusions:
PEC, macrophage and podocyte might play important roles in the formation of crescents. The staining disparity of nestin and podocalyxin indicates that podocyte dedifferentiation may occur during the crescent formation. PEC, podocytes and macrophages may participate in the formation of crescent in common CGNs through active cellular proliferation.
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