Laboratory of Molecular Cardiology, National Institutes of Health, Bethesda, MD 20892-1762.
Laboratory of Stem Cell and Neurovascular Biology, National Institutes of Health, Bethesda, MD 20892-1762.
Mol Biol Cell. 2020 Aug 15;31(18):1974-1987. doi: 10.1091/mbc.E20-03-0175. Epub 2020 Jun 17.
Among the three nonmuscle myosin 2 (NM2) paralogs, NM 2A and 2B, but not 2C, are detected in endothelial cells. To study the role of NM2 in vascular formation, we ablate NM2 in endothelial cells in mice. Ablating NM2A, but not NM2B, results in reduced blood vessel coverage and increased vascular branching in the developing mouse skin and coronary vasculature. NM2B becomes essential for vascular formation when NM2A expression is limited. Mice ablated for NM2B and one allele of NM2A develop vascular abnormalities similar to those in NM2A ablated mice. Using the embryoid body angiogenic sprouting assay in collagen gels reveals that NM2A is required for persistent angiogenic sprouting by stabilizing the endothelial cell cortex, and thereby preventing excessive branching and ensuring persistent migration of the endothelial sprouts. Mechanistically, NM2 promotes focal adhesion formation and cortical protrusion retraction during angiogenic sprouting. Further studies demonstrate the critical role of Rho kinase-activated NM2 signaling in the regulation of angiogenic sprouting in vitro and in vivo.
在三种非肌肉肌球蛋白 2(NM2)同工型中,内皮细胞中检测到 NM2A 和 2B,但检测不到 2C。为了研究 NM2 在血管形成中的作用,我们在小鼠内皮细胞中敲除 NM2。敲除 NM2A 而不是 NM2B 会导致发育中的小鼠皮肤和冠状动脉血管中血管覆盖减少和分支增加。当 NM2A 表达受到限制时,NM2B 对血管形成变得必不可少。敲除 NM2B 和 NM2A 的一个等位基因的小鼠会出现类似于 NM2A 敲除小鼠的血管异常。使用胶原凝胶中的胚状体血管生成发芽测定揭示,NM2A 通过稳定内皮细胞皮质来维持持久的血管生成发芽,从而防止过度分支并确保内皮芽持续迁移。从机制上讲,NM2 在血管生成发芽过程中促进粘着斑形成和皮质突起回缩。进一步的研究表明,Rho 激酶激活的 NM2 信号在调节体外和体内血管生成发芽中起着关键作用。