Department of Pharmacology, University of Michigan Medical Center, Ann Arbor, MI 48109.
Department of Medicine, Boston Children's Hospital and Harvard Medical School, Boston, MA 02115.
Proc Natl Acad Sci U S A. 2020 Nov 10;117(45):28275-28286. doi: 10.1073/pnas.2008921117. Epub 2020 Oct 23.
Circulating platelets roll along exposed collagen at vessel injury sites and respond with filipodia protrusion, shape change, and surface area expansion to facilitate platelet adhesion and plug formation. Various glycoproteins were considered to be both collagen responders and mediators of platelet adhesion, yet the signaling kinetics emanating from these receptors do not fully account for the rapid platelet cytoskeletal changes that occur in blood flow. We found the free N-terminal fragment of the adhesion G protein-coupled receptor (GPCR) GPR56 in human plasma and report that GPR56 is the platelet receptor that transduces signals from collagen and blood flow-induced shear force to activate G protein 13 signaling for platelet shape change. mice have prolonged bleeding, defective platelet plug formation, and delayed thrombotic occlusion. Human and mouse blood perfusion studies demonstrated GPR56 and shear-force dependence of platelet adhesion to immobilized collagen. Our work places GPR56 as an initial collagen responder and shear-force transducer that is essential for platelet shape change during hemostasis.
在血管损伤部位,循环血小板沿暴露的胶原蛋白滚动,并通过片状伪足伸出、形状改变和表面积扩大来响应,以促进血小板黏附和栓子形成。各种糖蛋白被认为既是胶原蛋白的响应者,也是血小板黏附的介质,但这些受体发出的信号动力学并不能完全解释发生在血流中的血小板细胞骨架的快速变化。我们在人血浆中发现了黏附 G 蛋白偶联受体(GPCR)GPR56 的游离 N 端片段,并报告 GPR56 是血小板受体,它将来自胶原蛋白和血流诱导的切应力的信号转导,以激活 G 蛋白 13 信号通路,从而引起血小板形状改变。GPR56 缺失小鼠表现出出血时间延长、血小板栓子形成缺陷和血栓闭塞延迟。人和小鼠的血液灌注研究表明,GPR56 及其对血小板与固定化胶原蛋白黏附的切应力依赖性。我们的工作将 GPR56 确定为初始胶原蛋白响应者和切应力传感器,这对于止血过程中的血小板形状改变至关重要。