Genomics Institute of the Novartis Research Foundation, San Diego, CA 92121, USA.
MITOVASC Institute, CARFI Facility, CNRS UMR 6015, INSERM U1083, Angers University, Angers, France.
Cell. 2018 Apr 19;173(3):762-775.e16. doi: 10.1016/j.cell.2018.03.076.
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.
机械转导在血管生物学中起着至关重要的作用。一个例子是通过血流介导的扩张(FMD)对血管阻力进行局部调节。这个过程的损伤是血管内皮功能障碍的标志,也是广泛的血管疾病(如高血压和动脉粥样硬化)的前兆。然而,负责在内皮细胞中感知流动(切应力)的分子在很大程度上仍然未知。我们设计了一种 384 孔筛选系统,用于对培养细胞施加切应力。我们鉴定了一种机械敏感的细胞系,该细胞系表现出切应力激活的钙瞬变,筛选了一个聚焦的 RNAi 文库,并鉴定了 GPR68 是切应力反应所必需和充分的。GPR68 在小直径(阻力)动脉的内皮细胞中表达。重要的是,Gpr68 缺陷小鼠表现出明显受损的急性 FMD 和慢性血流介导的肠系膜小动脉外向重塑。因此,GPR68 是血管内皮中必不可少的流传感器,也是心血管病理生理学中的关键信号成分。