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血管内皮细胞瞬时受体电位通道的最新进展

Recent developments in vascular endothelial cell transient receptor potential channels.

作者信息

Yao Xiaoqiang, Garland Christopher J

机构信息

Department of Physiology, Chinese University of Hong Kong, China.

出版信息

Circ Res. 2005 Oct 28;97(9):853-63. doi: 10.1161/01.RES.0000187473.85419.3e.

Abstract

Among the 28 identified and unique mammalian TRP (transient receptor potential) channel isoforms, at least 19 are expressed in vascular endothelial cells. These channels appear to participate in a diverse range of vascular functions, including control of vascular tone, regulation of vascular permeability, mechanosensing, secretion, angiogenesis, endothelial cell proliferation, and endothelial cell apoptosis and death. Malfunction of these channels may result in disorders of the human cardiovascular system. All TRP channels, except for TRPM4 and TRPM5, are cation channels that allow Ca2+ influx. However, there is a daunting diversity in the mode of activation and regulation in each case. Specific TRP channels may be activated by different stimuli such as vasoactive agents, oxidative stress, mechanical stimuli, and heat. TRP channels may then transform these stimuli into changes in the cytosolic Ca2+, which are eventually coupled to various vascular responses. Evidence has been provided to suggest the involvement of at least the following TRP channels in vascular function: TRPC1, TRPC4, TRPC6, and TRPV1 in the control of vascular permeability; TRPC4, TRPV1, and TRPV4 in the regulation of vascular tone; TRPC4 in hypoxia-induced vascular remodeling; and TRPC3, TRPC4, and TRPM2 in oxidative stress-induced responses. However, in spite of the large body of data available, the functional role of many endothelial TRP channels is still poorly understood. Elucidating the mechanisms regulating the different endothelial TRP channels, and the associated development of drugs selectively to target the different isoforms, as a means to treat cardiovascular disease should, therefore, be a high priority.

摘要

在已鉴定出的28种独特的哺乳动物瞬时受体电位(TRP)通道亚型中,至少有19种在血管内皮细胞中表达。这些通道似乎参与了多种血管功能,包括血管张力的控制、血管通透性的调节、机械传感、分泌、血管生成、内皮细胞增殖以及内皮细胞凋亡和死亡。这些通道功能异常可能导致人类心血管系统紊乱。除TRPM4和TRPM5外,所有TRP通道都是允许Ca2+内流的阳离子通道。然而,每种通道的激活和调节方式存在巨大差异。特定的TRP通道可能被不同的刺激激活,如血管活性物质、氧化应激、机械刺激和热。然后,TRP通道可将这些刺激转化为胞质Ca2+的变化,最终与各种血管反应相偶联。已有证据表明至少以下TRP通道参与血管功能:TRPC1、TRPC4、TRPC6和TRPV1参与血管通透性的控制;TRPC4、TRPV1和TRPV4参与血管张力的调节;TRPC4参与缺氧诱导的血管重塑;TRPC3、TRPC4和TRPM2参与氧化应激诱导的反应。然而,尽管有大量数据,但许多内皮TRP通道的功能作用仍知之甚少。因此,阐明调节不同内皮TRP通道的机制以及开发选择性靶向不同亚型的药物作为治疗心血管疾病的手段应成为高度优先事项。

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