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单体非 RhoA GTPase 对平滑肌收缩的调节。

Regulation of smooth muscle contraction by monomeric non-RhoA GTPases.

机构信息

Department of Urology, University Hospital, LMU Munich, Munich, Germany.

出版信息

Br J Pharmacol. 2020 Sep;177(17):3865-3877. doi: 10.1111/bph.15172. Epub 2020 Jul 19.

Abstract

Smooth muscle contraction in the cardiovascular system, airways, prostate and lower urinary tract is involved in the pathophysiology of many diseases, including cardiovascular and obstructive lung disease plus lower urinary tract symptoms, which are associated with high prevalence of morbidity and mortality. This prominent clinical role of smooth muscle tone has led to the molecular mechanisms involved being subjected to extensive research. In general smooth muscle contraction is promoted by three major signalling pathways, including the monomeric GTPase RhoA pathway. However, emerging evidence suggests that monomeric GTPases other than RhoA may be involved in signal transduction in smooth muscle contraction, including Rac GTPases, cell division control protein 42 homologue, adenosine ribosylation factor 6, Ras, Rap1b and Rab GTPases. Here, we review these emerging functions of non-RhoA GTPases in smooth muscle contraction, which has now become increasingly more evident and constitutes an emerging and innovative research area of high clinical relevance.

摘要

心血管系统、气道、前列腺和下尿路的平滑肌收缩参与了许多疾病的病理生理学过程,包括心血管疾病和阻塞性肺病以及下尿路症状,这些疾病与高发病率和死亡率相关。平滑肌张力的这种突出的临床作用导致了涉及的分子机制受到广泛研究。一般来说,平滑肌收缩是由三个主要的信号通路促进的,包括单体 GTPase RhoA 通路。然而,新出现的证据表明,除了 RhoA 之外,单体 GTPases 可能参与平滑肌收缩的信号转导,包括 Rac GTPases、细胞分裂控制蛋白 42 同源物、腺苷核糖基化因子 6、Ras、Rap1b 和 Rab GTPases。在这里,我们回顾了这些非 RhoA GTPases 在平滑肌收缩中的新功能,这一点现在变得越来越明显,并且构成了一个具有高度临床相关性的新兴和创新的研究领域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a0c/7429483/83adb1519621/BPH-177-3865-g001.jpg

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