p38 MAPK activation and STIM1-Orai3 association mediate TRPC6 externalization

Author:

Chaudhuri Pinaki12,Putta Priya1ORCID,Rosenbaum Michael A.12ORCID,Graham Linda M.13ORCID

Affiliation:

1. Department of Biomedical Engineering, Cleveland Clinic, Cleveland, Ohio, United States

2. Surgical Service, Louis B. Stokes Cleveland Veterans Affairs Medical Center, Cleveland, Ohio, United States

3. Department of Vascular Surgery, Cleveland Clinic, Cleveland, Ohio, United States

Abstract

The major lysophospholipid component in oxidized LDL, lysophosphatidylcholine (lysoPC), can activate p38 MAP kinase, which in turn promotes externalization of Orai3 and STIM1-Orai3 association, suggesting involvement of arachidonic acid-regulated calcium (ARC) channels. The subsequent increase in intracellular calcium activates an Src kinase required for TRPC6 externalization. TRPC6 activation, which has been shown to inhibit endothelial cell migration, is blocked by p38 MAP kinase or Orai3 downregulation, and this partially preserves endothelial migration in lysoPC.

Funder

HHS | NIH | National Heart, Lung, and Blood Institute

U.S. Department of Veterans Affairs

Publisher

American Physiological Society

Subject

Cell Biology,Physiology

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. A Putative Role for TRPC6 in Immune-Mediated Kidney Injury;International Journal of Molecular Sciences;2023-11-16

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