Piezo1 links mechanical forces to red blood cell volume

eLife

Michael Bandell¹  Shu Chien²  Stuart M Cahalan³  Viktor Lukacs³  Sanjeev S Ranade³  Ardem Patapoutian⁴ 

[1] Institute of Engineering in Medicine, University of California, San Diego, San Diego, United States;Department of Bioengineering, University of California, San Diego, San Diego, United States;Department of Molecular and Cellular Neuroscience, Howard Hughes Medical Institute, The Scripps Research Institute, La Jolla, United States;Genomics Institute of the Novartis Research Foundation, San Diego, United States;

关键词: red blood cell;    mechanotransduction;    physiology;    cell volume regulation;    knockout animal;   

DOI  :  10.7554/eLife.07370

来源: DOAJ

【 摘 要 】

Red blood cells (RBCs) experience significant mechanical forces while recirculating, but the consequences of these forces are not fully understood. Recent work has shown that gain-of-function mutations in mechanically activated Piezo1 cation channels are associated with the dehydrating RBC disease xerocytosis, implicating a role of mechanotransduction in RBC volume regulation. However, the mechanisms by which these mutations result in RBC dehydration are unknown. In this study, we show that RBCs exhibit robust calcium entry in response to mechanical stretch and that this entry is dependent on Piezo1 expression. Furthermore, RBCs from blood-cell-specific Piezo1 conditional knockout mice are overhydrated and exhibit increased fragility both in vitro and in vivo. Finally, we show that Yoda1, a chemical activator of Piezo1, causes calcium influx and subsequent dehydration of RBCs via downstream activation of the KCa3.1 Gardos channel, directly implicating Piezo1 signaling in RBC volume control. Therefore, mechanically activated Piezo1 plays an essential role in RBC volume homeostasis.

【 授权许可】

Unknown