RhoA/ rho激酶信号传导的新见解:血管收缩的关键调节因子。

Q2 Biochemistry, Genetics and Molecular Biology
Small GTPases Pub Date : 2021-09-01 Epub Date: 2020-09-24 DOI:10.1080/21541248.2020.1822721
Kenia Pedrosa Nunes, R Clinton Webb
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引用次数: 15

摘要

虽然rho信号控制血管收缩是一个典型的机制,但随着研究中使用的现代方法,我们正在推进对这一途径的理解和细节经常被发现。rhoa介导的rho激酶是血管平滑肌细胞的主要调节因子,也是操纵这些细胞其他功能的关键参与者。新的相互作用的发现,如氧化应激和硫化氢与Rho信号不仅在平滑肌的生理,而且在血管疾病的病理生理方面正在出现。同样,衰老和rho激酶在脉管系统中的相互作用最近也被考虑。重要的是,在平滑肌收缩中,这一途径也可能受到性激素的影响,因此也受到性别差异的影响。本文综述了Rho信号介导血管收缩的研究,并重点讨论了影响这一途径的最新文献,如衰老、性别差异和氧化应激。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

New insights into RhoA/Rho-kinase signaling: a key regulator of vascular contraction.

New insights into RhoA/Rho-kinase signaling: a key regulator of vascular contraction.

While Rho-signalling controlling vascular contraction is a canonical mechanism, with the modern approaches used in research, we are advancing our understanding and details into this pathway are often uncovered. RhoA-mediated Rho-kinase is the major regulator of vascular smooth muscle cells and a key player manoeuvring other functions in these cells. The discovery of new interactions, such as oxidative stress and hydrogen sulphide with Rho signalling are emerging addition not only in the physiology of the smooth muscle, but especially in the pathophysiology of vascular diseases. Likewise, the interplay between ageing and Rho-kinase in the vasculature has been recently considered. Importantly, in smooth muscle contraction, this pathway may also be affected by sex hormones, and consequently, sex-differences. This review provides an overview of Rho signalling mediating vascular contraction and focuses on recent topics discussed in the literature affecting this pathway such as ageing, sex differences and oxidative stress.

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来源期刊
Small GTPases
Small GTPases Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
6.10
自引率
0.00%
发文量
6
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