Fine Noah, Dimitriou Ioannis D, Rottapel Robert
Matrix Dynamics Group, University of Toronto, Toronto, Ontario, Canada.
Princess Margaret Cancer Center, Toronto Medical Discovery Tower, Toronto, Ontario, Canada.
Small GTPases. 2020 Jan;11(1):23-31. doi: 10.1080/21541248.2017.1332505. Epub 2017 Nov 30.
Neutrophils in circulation experience significant shear forces due to blood flow when they tether to the vascular endothelium. Biochemical and biophysical responses of neutrophils to the physical force of flowing blood modulate their behavior and promote tissue recruitment under pro-inflammatory conditions. Neutrophil mechanotransduction responses occur through mechanisms that are not yet fully understood. In our recent work, we showed that GEF-H1, a RhoA specific guanine nucleotide exchange factor (GEF), is required to maintain neutrophil motility and migration in response to shear stress. GEF-H1 re-localizes to flottilin-rich uropods in neutrophils in response to fluid shear stress and promotes spreading and crawling on activated endothelial cells. GEF-H1 drives cellular contractility through myosin light chain (MLC) phosphorylation downstream of the Rho-ROCK signaling axis. We propose that GEF-H1-dependent cell spreading and crawling in shear stress-dependent neutrophil recruitment from the vasculature are due to the specific localization of Rho-induced contractility in the uropod.
循环中的中性粒细胞在与血管内皮细胞结合时会因血流而受到显著的剪切力。中性粒细胞对流动血液的物理力的生化和生物物理反应会调节其行为,并在促炎条件下促进组织募集。中性粒细胞的机械转导反应通过尚未完全了解的机制发生。在我们最近的工作中,我们表明,GEF-H1是一种RhoA特异性鸟嘌呤核苷酸交换因子(GEF),是维持中性粒细胞在剪切应力下的运动性和迁移所必需的。响应流体剪切应力,GEF-H1重新定位于中性粒细胞中富含弗洛蒂林的尾足,并促进在活化内皮细胞上的铺展和爬行。GEF-H1通过Rho-ROCK信号轴下游的肌球蛋白轻链(MLC)磷酸化驱动细胞收缩性。我们提出,在依赖剪切应力的中性粒细胞从脉管系统募集中,GEF-H1依赖性细胞铺展和爬行是由于尾足中Rho诱导的收缩性的特定定位。