生物
肾素-血管紧张素系统
调节器
球旁器
细胞生物学
机械转化
肾
谱系(遗传)
电池类型
激活剂(遗传学)
内科学
内分泌学
钙
细胞
旁分泌信号
细胞功能
灌注
功能(生物学)
免疫学
细胞谱系
钙通道
作者
Rose Z. Hill,Jonathan W. Nelson,Georgina Gyarmati,Silvia Medrano,Sepenta Shirvan,James A. McCormick,Sebastian Burquez,J. Ahmed,Diana G. Eng,Jan Wysocki,Adrienne E. Dubin,M Rocio Servin-Vences,Arjun Lakshmanan,R. Ariel Gómez,Maria Luisa S. Sequeira-Lόpez,Stuart J. Shankland,Daniel Batlle,Jeffrey H. Miner,János Peti‐Peterdi,Ardem Patapoutian
出处
期刊:Cell
[Cell Press]
日期:2025-12-04
卷期号:189 (1): 161-178.e22
被引量:5
标识
DOI:10.1016/j.cell.2025.11.013
摘要
Renin synthesis and release is the rate-limiting step of the renin-angiotensin-aldosterone system (RAAS) that controls fluid homeostasis. A major activator of the RAAS is a decrease in perfusion pressure within the kidneys, suggesting a link between renal mechanotransduction and renin. However, the identity of the mechanosensor(s) in the kidneys and their physiological significance to the RAAS remain unclear. We find that loss of the force-gated nonselective cation channel PIEZO2 in cells of renin lineage dysregulates the RAAS by elevating renin. We observe that PIEZO2 is expressed in renin-producing juxtaglomerular granular cells and is required for their calcium dynamics in vivo. PIEZO2 deficiency in cells of renin lineage drives renin-dependent and MAS-receptor-dependent glomerular hyperfiltration and regulates the RAAS during acute and chronic blood volume challenges. Collectively, our study identifies PIEZO2 as an essential regulator of juxtaglomerular granular cell calcium activity and renin in vivo.
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