Rocking the Boat: The Decisive Roles of Rho Kinases During Oocyte, Blastocyst, and Stem Cell Development

被引:10
|
作者
Saadeldin, Islam M. [1 ,2 ]
Tukur, Hammed A. [1 ]
Aljumaah, Riyadh S. [1 ]
Sindi, Ramya A. [3 ]
机构
[1] King Saud Univ, Dept Anim Prod, Coll Food & Agr Sci, Riyadh, Saudi Arabia
[2] King Faisal Specialist Hosp & Res Ctr, Dept Comparat Med, Riyadh, Saudi Arabia
[3] Umm Al Qura Univ, Fac Appl Med Sci, Dept Lab Med, Mecca, Saudi Arabia
关键词
rho kinase; oocyte; stem cells; differentiation; actin; INHIBITOR Y-27632; COILED-COIL; SERINE/THREONINE KINASE; DISTINCT ROLES; BINDING; PHOSPHORYLATION; DIFFERENTIATION; ACTIVATION; PROTEINS; ISOFORMS;
D O I
10.3389/fcell.2020.616762
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The rho-associated coiled-coil-containing proteins (ROCKs or rho kinase) are effectors of the small rho-GTPase rhoA, which acts as a signaling molecule to regulate a variety of cellular processes, including cell proliferation, adhesion, polarity, cytokinesis, and survival. Owing to the multifunctionality of these kinases, an increasing number of studies focus on understanding the pleiotropic effects of the ROCK signaling pathway in the coordination and control of growth (proliferation, initiation, and progression), development (morphology and differentiation), and survival in many cell types. There is growing evidence that ROCKs actively phosphorylate several actin-binding proteins and intermediate filament proteins during oocyte cytokinesis, the preimplantation embryos as well as the stem cell development and differentiation. In this review, we focus on the participation of ROCK proteins in oocyte maturation, blastocyst formation, and stem cell development with a special focus on the selective targeting of ROCK isoforms, ROCK1, and ROCK2. The selective switching of cell fate through ROCK inhibition would provide a novel paradigm for in vitro oocyte maturation, experimental embryology, and clinical applications.
引用
收藏
页数:10
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