Department of Medical Pharmacology and Physiology, University of Missouri School of Medicine, Columbia, Missouri, USA.
Int Rev Cell Mol Biol. 2011;288:101-65. doi: 10.1016/B978-0-12-386041-5.00003-0.
Many studies reveal a fundamental role for extracellular matrix-mediated signaling through integrins and Rho GTPases as well as matrix metalloproteinases (MMPs) in the molecular control of vascular tube morphogenesis in three-dimensional (3D) tissue environments. Recent work has defined an endothelial cell (EC) lumen signaling complex of proteins that controls these vascular morphogenic events. These findings reveal a signaling interdependence between Cdc42 and MT1-MMP to control the 3D matrix-specific process of EC tubulogenesis. The EC tube formation process results in the creation of a network of proteolytically generated vascular guidance tunnels in 3D matrices that are utilized to remodel EC-lined tubes through EC motility and could facilitate processes such as flow-induced remodeling and arteriovenous EC sorting and differentiation. Within vascular guidance tunnels, key dynamic interactions occur between ECs and pericytes to affect vessel remodeling, diameter, and vascular basement membrane matrix assembly, a fundamental process necessary for endothelial tube maturation and stabilization. Thus, the EC lumen and tube formation mechanism coordinates the concomitant establishment of a network of vascular tubes within tunnel spaces to allow for flow responsiveness, EC-mural cell interactions, and vascular extracellular matrix assembly to control the development of the functional microcirculation.
许多研究揭示了细胞外基质通过整合素和 Rho GTPases 以及基质金属蛋白酶(MMPs)介导的信号在三维(3D)组织环境中血管管腔形态发生的分子控制中的基本作用。最近的工作定义了一个控制这些血管形态发生事件的内皮细胞(EC)管腔信号复合物蛋白。这些发现揭示了 Cdc42 和 MT1-MMP 之间的信号相互依赖性,以控制 EC 小管形成的 3D 基质特异性过程。EC 管形成过程导致在 3D 基质中产生一系列蛋白水解生成的血管导向隧道网络,这些网络用于通过 EC 迁移重塑 EC 衬里的管腔,并可能促进诸如流诱导重塑和动静脉 EC 分类和分化等过程。在血管导向隧道内,EC 和周细胞之间发生关键的动态相互作用,影响血管重塑、直径和血管基底膜基质组装,这是内皮管成熟和稳定所必需的基本过程。因此,EC 管腔和管形成机制协调在隧道空间内建立血管管腔网络,以允许对流动反应性、EC-壁细胞相互作用和血管细胞外基质组装进行控制,从而控制功能性微循环的发育。