| Literature DB >> 29677517 |
Jie Xu1, Jayanti Mathur1, Emilie Vessières2, Scott Hammack1, Keiko Nonomura3, Julie Favre2, Linda Grimaud2, Matt Petrus1, Allain Francisco3, Jingyuan Li1, Van Lee1, Fu-Li Xiang1, James K Mainquist1, Stuart M Cahalan3, Anthony P Orth1, John R Walker1, Shang Ma3, Viktor Lukacs3, Laura Bordone1, Michael Bandell1, Bryan Laffitte1, Yan Xu4, Shu Chien5, Daniel Henrion2, Ardem Patapoutian6.
Abstract
Mechanotransduction plays a crucial role in vascular biology. One example of this is the local regulation of vascular resistance via flow-mediated dilation (FMD). Impairment of this process is a hallmark of endothelial dysfunction and a precursor to a wide array of vascular diseases, such as hypertension and atherosclerosis. Yet the molecules responsible for sensing flow (shear stress) within endothelial cells remain largely unknown. We designed a 384-well screening system that applies shear stress on cultured cells. We identified a mechanosensitive cell line that exhibits shear stress-activated calcium transients, screened a focused RNAi library, and identified GPR68 as necessary and sufficient for shear stress responses. GPR68 is expressed in endothelial cells of small-diameter (resistance) arteries. Importantly, Gpr68-deficient mice display markedly impaired acute FMD and chronic flow-mediated outward remodeling in mesenteric arterioles. Therefore, GPR68 is an essential flow sensor in arteriolar endothelium and is a critical signaling component in cardiovascular pathophysiology.Entities:
Keywords: GPCR; blood flow; mechanosensation; mechanotransduction; outward remodeling; shear stress; vascular biology; vasodilation
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Year: 2018 PMID: 29677517 PMCID: PMC5951615 DOI: 10.1016/j.cell.2018.03.076
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582