Laboratory for Vascular Morphogenesis, RIKEN Center for Biosystems Dynamics Research, Kobe, 650-0047, Japan.
Bioimage Informatics Group, Exploratory Research Center on Life and Living Systems (ExCELLS), National Institutes of Natural Sciences, Okazaki, Aichi, 444-8585, Japan.
Nat Commun. 2020 Oct 30;11(1):5476. doi: 10.1038/s41467-020-19308-5.
The formation of vascular tubes is driven by extensive changes in endothelial cell (EC) shape. Here, we have identified a role of the actin-binding protein, Marcksl1, in modulating the mechanical properties of EC cortex to regulate cell shape and vessel structure during angiogenesis. Increasing and depleting Marcksl1 expression level in vivo results in an increase and decrease, respectively, in EC size and the diameter of microvessels. Furthermore, endothelial overexpression of Marcksl1 induces ectopic blebbing on both apical and basal membranes, during and after lumen formation, that is suppressed by reduced blood flow. High resolution imaging reveals that Marcksl1 promotes the formation of linear actin bundles and decreases actin density at the EC cortex. Our findings demonstrate that a balanced network of linear and branched actin at the EC cortex is essential in conferring cortical integrity to resist the deforming forces of blood flow to regulate vessel structure.
血管管腔的形成是由内皮细胞(EC)形状的广泛变化所驱动的。在这里,我们确定了肌动蛋白结合蛋白 Marcksl1 的一个作用,即调节 EC 皮质的机械特性,以在血管生成过程中调节细胞形状和血管结构。体内增加和耗尽 Marcksl1 的表达水平分别导致 EC 大小和微血管直径增加和减少。此外,内皮细胞中 Marcksl1 的过表达会在腔形成期间和之后诱导顶端和基底膜上的异位泡状突起,而减少血流会抑制这种突起。高分辨率成像显示,Marcksl1 促进了线性肌动蛋白束的形成,并降低了 EC 皮质处的肌动蛋白密度。我们的研究结果表明,EC 皮质处线性和分支肌动蛋白的平衡网络对于赋予皮质完整性以抵抗血流的变形力从而调节血管结构是至关重要的。