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血管钙信号与衰老。

Vascular calcium signalling and ageing.

机构信息

Department of Pharmacology, Larner College of Medicine, University of Vermont, Burlington, Vermont, USA.

Vermont Center for Cardiovascular and Brain Health, University of Vermont, Burlington, Vermont, USA.

出版信息

J Physiol. 2021 Dec;599(24):5361-5377. doi: 10.1113/JP280950. Epub 2021 Nov 21.

Abstract

Changes in cellular Ca levels have major influences on vascular function and blood pressure regulation. Vascular smooth muscle cells (SMCs) and endothelial cells (ECs) orchestrate vascular activity in distinct ways, often involving highly specific fluctuations in Ca signalling. Ageing is a major risk factor for cardiovascular diseases, but the impact of ageing per se on vascular Ca signalling has received insufficient attention. We reviewed the literature for age-related changes in Ca signalling in relation to vascular structure and function. Vascular tone dysregulation in several vascular beds has been linked to abnormal expression or activity of SMC voltage-gated Ca channels, Ca -activated K channels or TRPC6 channels. Some of these effects were linked to altered caveolae density, microRNA expression or 20-HETE abundance. Intracellular store Ca handling was suppressed in ageing mainly via reduced expression of intracellular Ca release channels, and Ca reuptake or efflux pumps. An increase in mitochondrial Ca uptake, leading to oxidative stress, could also play a role in SMC hypercontractility and structural remodelling in ageing. In ECs, ageing entailed diverse effects on spontaneous and evoked Ca transients, as well as structural changes at the EC-SMC interface. The concerted effects of altered Ca signalling on myogenic tone, endothelium-dependent vasodilatation, and vascular structure are likely to contribute to blood pressure dysregulation and blood flow distribution deficits in critical organs. With the increase in the world's ageing population, future studies should be directed at solving specific ageing-induced Ca signalling deficits to combat the imminent accelerated vascular ageing and increased risk of cardiovascular diseases.

摘要

细胞内钙水平的变化对血管功能和血压调节有重大影响。血管平滑肌细胞 (SMCs) 和内皮细胞 (ECs) 以不同的方式协调血管活动,通常涉及钙信号的高度特异性波动。衰老是心血管疾病的一个主要危险因素,但衰老本身对血管钙信号的影响尚未得到足够的重视。我们回顾了与血管结构和功能相关的钙信号随年龄变化的文献。几个血管床的血管张力失调与 SMC 电压门控钙通道、钙激活的 K 通道或 TRPC6 通道的异常表达或活性有关。其中一些影响与 caveolae 密度、microRNA 表达或 20-HETE 丰度的改变有关。衰老时细胞内钙储存的处理受到抑制,主要是通过减少细胞内钙释放通道、钙摄取或外排泵的表达。线粒体摄取钙的增加导致氧化应激,也可能在 SMC 过度收缩和衰老时的结构重塑中发挥作用。在内皮细胞中,衰老对自发和诱发钙瞬变以及内皮细胞 - 平滑肌细胞界面的结构变化产生了多种影响。钙信号改变对肌源性张力、内皮依赖性血管舒张以及血管结构的协同作用可能导致血压失调和重要器官的血流分布缺陷。随着世界人口老龄化的增加,未来的研究应该致力于解决特定的衰老诱导的钙信号缺陷,以对抗即将加速的血管老化和心血管疾病风险的增加。

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