Norden Pieter R, Kim Dae Joong, Barry David M, Cleaver Ondine B, Davis George E
Department of Medical Pharmacology and Physiology, University of Missouri School of Medicine, Dalton Cardiovascular Research Center, Columbia, MO, United States of America.
Department of Molecular Biology, UT Southwestern Medical Center, Dallas, TX, United States of America.
PLoS One. 2016 Jan 26;11(1):e0147758. doi: 10.1371/journal.pone.0147758. eCollection 2016.
A critical and understudied property of endothelial cells is their ability to form lumens and tube networks. Although considerable information has been obtained concerning these issues, including the role of Cdc42 and Rac1 and their effectors such as Pak2, Pak4, Par6b, and co-regulators such as integrins, MT1-MMP and Par3; many key questions remain that are necessary to elucidate molecular and signaling requirements for this fundamental process. In this work, we identify new small GTPase regulators of EC tubulogenesis including k-Ras, Rac2 and Rap1b that act in conjunction with Cdc42 as well as the key downstream effectors, IQGAP1, MRCKβ, beta-Pix, GIT1, and Rasip1 (which can assemble into multiprotein complexes with key regulators including α2β1 integrin and MT1-MMP). In addition, we identify the negative regulators, Arhgap31 (by inactivating Cdc42 and Rac) and Rasa1 (by inactivating k-Ras) and the positive regulator, Arhgap29 (by inactivating RhoA) which play a major functional role during the EC tubulogenic process. Human EC siRNA suppression or mouse knockout of Rasip1 leads to identical phenotypes where ECs form extensive cord networks, but cannot generate lumens or tubes. Essential roles for these molecules during EC tubulogenesis include; i) establishment of asymmetric EC cytoskeletal polarization (subapical distribution of acetylated tubulin and basal membrane distribution of F-actin); and ii) directed membrane trafficking of pinocytic vacuoles or other intracellular vesicles along acetylated tubulin tracks to the developing apical membrane surface. Cdc42 co-localizes subapically with acetylated tubulin, while Rac1 and k-Ras strongly label vacuole/ vesicle membranes which accumulate and fuse together in a polarized, perinuclear manner. We observe polarized apical membrane and subapical accumulation of key GTPases and effectors regulating EC lumen formation including Cdc42, Rac1, Rac2, k-Ras, Rap1b, activated c-Raf and Rasip1 to control EC tube network assembly. Overall, this work defines novel key regulators and their functional roles during human EC tubulogenesis.
内皮细胞一个关键且尚未得到充分研究的特性是其形成管腔和管网的能力。尽管已经获得了有关这些问题的大量信息,包括Cdc42和Rac1及其效应器(如Pak2、Pak4、Par6b)以及共调节因子(如整合素、MT1 - MMP和Par3)的作用;但仍存在许多关键问题,这些问题对于阐明这一基本过程的分子和信号需求至关重要。在这项研究中,我们鉴定出了内皮细胞微管生成的新的小GTP酶调节因子,包括与Cdc42协同作用的k - Ras、Rac2和Rap1b,以及关键的下游效应器IQGAP1、MRCKβ、β - Pix、GIT1和Rasip1(后者可与包括α2β1整合素和MT1 - MMP在内的关键调节因子组装成多蛋白复合物)。此外,我们还鉴定出了负调节因子Arhgap31(通过使Cdc42和Rac失活)和Rasa1(通过使k - Ras失活)以及正调节因子Arhgap29(通过使RhoA失活),它们在内皮细胞微管生成过程中发挥着主要功能作用。人内皮细胞的siRNA抑制或小鼠Rasip1基因敲除会导致相同的表型,即内皮细胞形成广泛的索状网络,但无法生成管腔或微管。这些分子在内皮细胞微管生成过程中的重要作用包括:i)建立不对称的内皮细胞细胞骨架极化(乙酰化微管蛋白的亚顶端分布和F - 肌动蛋白的基底膜分布);ii)将胞饮液泡或其他细胞内囊泡沿着乙酰化微管蛋白轨道定向运输到发育中的顶端膜表面。Cdc42与乙酰化微管蛋白在亚顶端共定位,而Rac1和k - Ras强烈标记液泡/囊泡膜,这些膜以极化的、核周的方式聚集并融合在一起。我们观察到调节内皮细胞管腔形成的关键GTP酶和效应器,包括Cdc42、Rac1、Rac2、k - Ras、Rap1b、活化的c - Raf和Rasip1,在内皮细胞顶端膜和亚顶端积累,以控制内皮细胞管网组装。总体而言,这项研究确定了人内皮细胞微管生成过程中的新型关键调节因子及其功能作用。