罗亚
岩石1
细胞生物学
斑马鱼
血管生成
生物
小型GTPase
体内
信号转导
应力纤维
癌症研究
焦点粘着
生物化学
遗传学
基因
作者
Laura M. Pillay,Joseph J. Yano,Andrew E. Davis,Matthew G. Butler,Megan O. Ezeude,Jong S. Park,Keith A. Barnes,Vanessa L. Reyes,Daniel Castranova,Aniket V. Gore,Matthew R. Swift,James R. Iben,Madeleine I. Kenton,Amber N. Stratman,Brant M. Weinstein
出处
期刊:Angiogenesis
[Springer Nature]
日期:2022-03-23
卷期号:25 (3): 411-434
被引量:2
标识
DOI:10.1007/s10456-022-09834-9
摘要
The small monomeric GTPase RHOA acts as a master regulator of signal transduction cascades by activating effectors of cellular signaling, including the Rho-associated protein kinases ROCK1/2. Previous in vitro cell culture studies suggest that RHOA can regulate many critical aspects of vascular endothelial cell (EC) biology, including focal adhesion, stress fiber formation, and angiogenesis. However, the specific in vivo roles of RHOA during vascular development and homeostasis are still not well understood. In this study, we examine the in vivo functions of RHOA in regulating vascular development and integrity in zebrafish. We use zebrafish RHOA-ortholog (rhoaa) mutants, transgenic embryos expressing wild type, dominant negative, or constitutively active forms of rhoaa in ECs, pharmacological inhibitors of RHOA and ROCK1/2, and Rock1 and Rock2a/b dgRNP-injected zebrafish embryos to study the in vivo consequences of RHOA gain- and loss-of-function in the vascular endothelium. Our findings document roles for RHOA in vascular integrity, developmental angiogenesis, and vascular morphogenesis in vivo, showing that either too much or too little RHOA activity leads to vascular dysfunction.
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