Department of Clinical Biochemistry and Immunohematology, Faculty of Health Sciences, Medical Technology School, Thrombosis and Healthy Aging Research Center, Universidad de Talca, Talca, Chile.
Centro Nacional de Investigaciones Cardiovasculares (CNIC), Madrid, Spain.
J Cell Mol Med. 2024 Apr;28(8):e18153. doi: 10.1111/jcmm.18153.
The small GTPase RhoA and the downstream Rho kinase (ROCK) regulate several cell functions and pathological processes in the vascular system that contribute to the age-dependent risk of cardiovascular disease, including endothelial dysfunction, excessive permeability, inflammation, impaired angiogenesis, abnormal vasoconstriction, decreased nitric oxide production and apoptosis. Frailty is a loss of physiological reserve and adaptive capacity with advanced age and is accompanied by a pro-inflammatory and pro-oxidative state that promotes vascular dysfunction and thrombosis. This review summarises the role of the RhoA/Rho kinase signalling pathway in endothelial dysfunction, the acquisition of the pro-thrombotic state and vascular ageing. We also discuss the possible role of RhoA/Rho kinase signalling as a promising therapeutic target for the prevention and treatment of age-related cardiovascular disease.
小 GTP 酶 RhoA 和下游的 Rho 激酶(ROCK)调节血管系统中的几种细胞功能和病理过程,这些过程导致心血管疾病的年龄依赖性风险增加,包括内皮功能障碍、通透性过高、炎症、血管生成受损、血管收缩异常、一氧化氮产生减少和细胞凋亡。衰弱是随着年龄增长而导致的生理储备和适应能力的丧失,伴随着促炎和促氧化状态,促进血管功能障碍和血栓形成。这篇综述总结了 RhoA/Rho 激酶信号通路在血管内皮功能障碍、促血栓形成状态和血管老化中的作用。我们还讨论了 RhoA/Rho 激酶信号作为预防和治疗与年龄相关的心血管疾病的有前途的治疗靶点的可能作用。