Renin Is Critical for Renin Lineage Cell Plasticity, Migration, and Disease Outcome in Experimental Crescentic Glomerulonephritis

肾素-血管紧张素系统 纤维化 足细胞 生物 内分泌学 内科学 炎症 巨噬细胞 细胞 肾小球肾炎 医学 肾脏疾病 蛋白尿 病理 癌症研究 川地68 细胞迁移 电池类型 转染 免疫学 共域化 巨噬细胞极化 局灶节段性肾小球硬化 血管紧张素II T细胞 细胞生物学 免疫系统 细胞培养 疾病 肾小球硬化 转录组 尼福林
作者
Shila Azizolli,Sagor Halder,Anne Steglich,Akua Annoh,Florian Gembardt,Irina Simonova,Jan Sradnick,Andreas Dahl,Rajinder K. Gupta,S Bornstein,Vladimir Todorov,Hannah Weissbach,Christian Hugo
出处
期刊:Journal of The American Society of Nephrology [American Society of Nephrology]
标识
DOI:10.1681/asn.0000001239
摘要

BACKGROUND: The adult juxtaglomerular renin-lineage cell niche demonstrates cellular plasticity following injury, but its role in highly inflammatory crescentic glomerulonephritis (crescentic GN) remains unclear. While renin-angiotensin signaling promotes fibrosis and inflammation, the contribution of the renin-lineage cells and renin expression within these cells to crescentic GN has not been investigated. METHODS: We used tdTomato (tdT) lineage-tracing to track renin-lineage cells in wild-type (WT) and renin-knockout (RenKO) mice following crescentic GN induction. Renin-lineage cell migration and glomerular injury were quantified histologically. Single-cell RNA sequencing was performed on isolated tdT+ cells at day 10 and 21 after injury to characterize transcriptional programs. Disease progression was additionally examined in mice with diphtheria toxin A-mediated (DTA) renin-lineage cell ablation. RESULTS: Renin-lineage cells were detected within injured glomeruli during crescentic GN. Genetic renin deletion worsened disease outcomes, with RenKO mice developing increased albuminuria (by 3-fold), crescent formation (by 50%) and podocyte loss (by 15%) by day 21 compared to WT controls. Renin-deficient renin-lineage cells exhibited reduced glomerular migration and decreased colocalization with mesangial cell markers. Single-cell transcriptomic analysis revealed distinct transcriptional programs between WT and RenKO renin-lineage cells, with RenKO cells enriched for interferon-stimulated and reduced migration-associated pathways. Renin-lineage cell ablation reduced macrophage infiltration, but did not alter disease severity. CONCLUSIONS: Renin expression influenced migration and injury-associated responses of renin-lineage cells during crescentic GN. Loss of renin was associated with a dysfunctional interferon-driven and anti-migratory phenotype together with more severe glomerular injury, whereas renin-lineage cell ablation reduced macrophage infiltration but had limited effects on overall disease severity.
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