University College London, Ludwig Institute for Cancer Research and Department of Biochemistry and Molecular Biology, London WC1E6BT, UK.
BMC Biol. 2010 Feb 2;8:11. doi: 10.1186/1741-7007-8-11.
Endothelial cell-cell junctions maintain endothelial integrity and regulate vascular morphogenesis and homeostasis. Cell-cell junctions are usually depicted with a linear morphology along the boundaries between adjacent cells and in contact with cortical F-actin. However, in the endothelium, cell-cell junctions are highly dynamic and morphologically heterogeneous.
We report that endothelial cell-cell junctions can attach to the ends of stress fibres instead of to cortical F-actin, forming structures that we name discontinuous adherens junctions (AJ). Discontinuous AJ are highly dynamic and are increased in response to tumour necrosis factor (TNF)-alpha, correlating with the appearance of stress fibres. We show that vascular endothelial (VE)-cadherin/beta-catenin/alpha-catenin complexes in discontinuous AJ are linked to stress fibres. Moreover, discontinuous AJ connect stress fibres from adjacent cells independently of focal adhesions, of which there are very few in confluent endothelial cells, even in TNF-alpha-stimulated cells. RNAi-mediated knockdown of VE-cadherin, but not zonula occludens-1, reduces the linkage of stress fibres to cell-cell junctions, increases focal adhesions, and dramatically alters the distribution of these actin cables in confluent endothelial cells.
Our results indicate that stress fibres from neighbouring cells are physically connected through discontinuous AJ, and that stress fibres can be stabilized by AJ-associated multi-protein complexes distinct from focal adhesions.
内皮细胞-细胞连接维持内皮完整性,并调节血管形态发生和稳态。细胞-细胞连接通常沿着相邻细胞的边界呈现线性形态,并与皮质 F-actin 接触。然而,在内皮细胞中,细胞-细胞连接具有高度动态性和形态异质性。
我们报告称,内皮细胞-细胞连接可以附着在应力纤维的末端,而不是皮质 F-actin 上,形成我们称之为不连续黏附连接(AJ)的结构。不连续 AJ 具有高度动态性,并在肿瘤坏死因子(TNF)-α的刺激下增加,与应力纤维的出现相关。我们表明,不连续 AJ 中的血管内皮(VE)-钙黏蛋白/β-连环蛋白/α-连环蛋白复合物与应力纤维相连。此外,不连续 AJ 将来自相邻细胞的应力纤维与焦点粘连连接起来,即使在 TNF-α刺激的细胞中,焦点粘连也很少见。VE-钙黏蛋白的 RNAi 介导的敲低,但不是封闭蛋白-1,减少了应力纤维与细胞-细胞连接的连接,增加了焦点粘连,并显著改变了这些肌动蛋白电缆在融合内皮细胞中的分布。
我们的结果表明,来自相邻细胞的应力纤维通过不连续 AJ 物理连接,并且可以通过与焦点粘连不同的 AJ 相关多蛋白复合物来稳定应力纤维。