Tian Yufeng, Gawlak Grzegorz, O'Donnell James J, Birukova Anna A, Birukov Konstantin G
From the Lung Injury Center and Section of Pulmonary and Critical Care Medicine, Department of Medicine, University of Chicago, Chicago, Illinois 60637.
From the Lung Injury Center and Section of Pulmonary and Critical Care Medicine, Department of Medicine, University of Chicago, Chicago, Illinois 60637
J Biol Chem. 2016 May 6;291(19):10032-45. doi: 10.1074/jbc.M115.690487. Epub 2016 Feb 16.
High tidal volume mechanical ventilation and the resultant excessive mechanical forces experienced by lung vascular endothelium are known to lead to increased vascular endothelial leak, but the underlying molecular mechanisms remain incompletely understood. One reported mechanotransduction pathway of increased endothelial cell (EC) permeability caused by high magnitude cyclic stretch (18% CS) involves CS-induced activation of the focal adhesion associated signalosome, which triggers Rho GTPase signaling. This study identified an alternative pathway of CS-induced EC permeability. We show here that high magnitude cyclic stretch (18% CS) rapidly activates VEGF receptor 2 (VEGFR2) signaling by dissociating VEGFR2 from VE-cadherin at the cell junctions. This results in VEGFR2 activation, Src-dependent VE-cadherin tyrosine phosphorylation, and internalization leading to increased endothelial permeability. This process is also accompanied by CS-induced phosphorylation and internalization of PECAM1. Importantly, CS-induced endothelial barrier disruption was attenuated by VEGFR2 inhibition. 18% CS-induced EC permeability was linked to dissociation of cell junction scaffold afadin from the adherens junctions. Forced expression of recombinant afadin in pulmonary endothelium attenuated CS-induced VEGFR2 and VE-cadherin phosphorylation, preserved adherens junction integrity and VEGFR2·VE-cadherin complex, and suppressed CS-induced EC permeability. This study shows for the first time a mechanism whereby VEGFR2 activation mediates EC permeability induced by pathologically relevant cyclic stretch. In this mechanism, CS induces dissociation of the VE-cadherin·VEGFR2 complex localized at the adherens juctions, causing activation of VEGFR2, VEGFR2-mediated Src-dependent phosphorylation of VE-cadherin, disassembly of adherens junctions, and EC barrier failure.
已知高潮气量机械通气以及肺血管内皮细胞所经历的由此产生的过度机械力会导致血管内皮渗漏增加,但其潜在的分子机制仍未完全清楚。一种报道的由高强度循环拉伸(18% CS)引起的内皮细胞(EC)通透性增加的机械转导途径涉及CS诱导的粘着斑相关信号体的激活,这会触发Rho GTPase信号传导。本研究确定了CS诱导的EC通透性的另一种途径。我们在此表明,高强度循环拉伸(18% CS)通过在细胞连接处使VEGFR2与VE-钙粘蛋白解离,迅速激活VEGF受体2(VEGFR2)信号传导。这导致VEGFR2激活、Src依赖的VE-钙粘蛋白酪氨酸磷酸化以及内化,从而导致内皮通透性增加。这个过程还伴随着CS诱导的PECAM1磷酸化和内化。重要的是,VEGFR2抑制减弱了CS诱导的内皮屏障破坏。18% CS诱导的EC通透性与细胞连接支架afadin从粘着连接处解离有关。在肺内皮细胞中强制表达重组afadin可减弱CS诱导的VEGFR2和VE-钙粘蛋白磷酸化,保持粘着连接完整性和VEGFR2·VE-钙粘蛋白复合物,并抑制CS诱导的EC通透性。本研究首次展示了一种机制,即VEGFR2激活介导由病理相关循环拉伸诱导的EC通透性。在这种机制中,CS诱导位于粘着连接处的VE-钙粘蛋白·VEGFR2复合物解离,导致VEGFR2激活、VEGFR2介导的Src依赖的VE-钙粘蛋白磷酸化、粘着连接解体以及EC屏障功能障碍。