Schnittler Hans, Taha Muna, Schnittler Maria Odenthal, Taha Abdallah Abu, Lindemann Nico, Seebach Jochen
Institute of Anatomy and Vascular Biology, Westfälische Wilhelms-Universität Münster, Vesaliusweg 2-4, 48149, Münster, Germany,
Cell Tissue Res. 2014 Mar;355(3):529-43. doi: 10.1007/s00441-014-1856-2. Epub 2014 Mar 19.
The vascular endothelium is a cellular interface between the blood and the interstitial space of tissue, which controls the exchange of fluid, solutes and cells by both transcellular and paracellular means. To accomplish the demands on barrier function, the regulation of the endothelium requires quick and adaptive mechanisms. This is, among others, accomplished by actin dynamics that interdependently interact with both the VE-cadherin/catenin complex, the main components of the adherens type junctions in endothelium and the membrane cytoskeleton. Actin filaments in endothelium are components of super-structured protein assemblies that control a variety of dynamic processes such as endo- and exocytosis, shape change, cell-substrate along with cell-cell adhesion and cell motion. In endothelium, actin filaments are components of: (1) contractile actin bundles appearing as stress fibers and junction-associated circumferential actin filaments, (2) actin networks accompanied by endocytotic ruffles, lamellipodia at leading edges of migrating cells and junction-associated intermittent lamellipodia (JAIL) that dynamically maintain junction integrity, (3) cortical actin and (4) the membrane cytoskeleton. All these structures, most probably interact with cell junctions and cell-substrate adhesion sites. Due to the rapid growth in information, we aim to provide a bird's eye view focusing on actin filaments in endothelium and its functional relevance for entire cell and junction integrity, rather than discussing the detailed molecular mechanism for control of actin dynamics.
血管内皮是血液与组织间质空间之间的细胞界面,它通过跨细胞和细胞旁途径控制液体、溶质和细胞的交换。为满足对屏障功能的需求,内皮的调节需要快速且适应性的机制。这尤其通过肌动蛋白动力学来实现,肌动蛋白动力学与VE-钙黏蛋白/连环蛋白复合体相互依存地相互作用,VE-钙黏蛋白/连环蛋白复合体是内皮中黏附连接的主要成分以及膜细胞骨架。内皮中的肌动蛋白丝是超结构化蛋白质组装体的组成部分,这些组装体控制着各种动态过程,如胞吞和胞吐作用、形状变化、细胞与底物以及细胞与细胞间的黏附及细胞运动。在内皮中,肌动蛋白丝是以下结构的组成部分:(1)收缩性肌动蛋白束,表现为应力纤维和与连接相关的周向肌动蛋白丝;(2)伴有胞吞褶皱、迁移细胞前缘的片状伪足以及动态维持连接完整性的与连接相关的间歇性片状伪足(JAIL)的肌动蛋白网络;(3)皮质肌动蛋白;(4)膜细胞骨架。所有这些结构很可能与细胞连接和细胞与底物的黏附位点相互作用。鉴于信息的快速增长,我们旨在提供一个全景视角,聚焦于内皮中的肌动蛋白丝及其对整个细胞和连接完整性的功能相关性,而非讨论控制肌动蛋白动力学的详细分子机制。
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