Department of Pharmacology, Center for Molecular and Cellular Signaling in the Cardiovascular System, University of Nevada, Reno, School of Medicine, Reno, NV, United States.
Department of Pharmacology, Center for Molecular and Cellular Signaling in the Cardiovascular System, University of Nevada, Reno, School of Medicine, Reno, NV, United States.
Curr Top Membr. 2020;85:119-150. doi: 10.1016/bs.ctm.2020.01.009. Epub 2020 Feb 29.
The Ca-permeable, non-selective cation channel, TRPA1 (transient receptor potential ankyrin 1), is the sole member of the ankyrin TRP subfamily. TRPA1 channels are expressed on the plasma membrane of neurons as well as non-neuronal cell types, such as vascular endothelial cells. TRPA1 is activated by electrophilic compounds, including dietary molecules such as allyl isothiocyanate, a derivative of mustard. Endogenously, the channel is thought to be activated by reactive oxygen species and their metabolites, such as 4-hydroxynonenal (4-HNE). In the context of the vasculature, activation of TRPA1 channels results in a vasodilatory response mediated by two distinct mechanisms. In the first instance, TRPA1 is expressed in sensory nerves of the vasculature and, upon activation, mediates release of the potent dilator, calcitonin gene-related peptide (CGRP). In the second, work from our laboratory has demonstrated that TRPA1 is expressed in the endothelium of blood vessels exclusively in the cerebral vasculature, where its activation produces a localized Ca signal that results in dilation of cerebral arteries. In this chapter, we provide an in-depth overview of the biophysical and pharmacological properties of TRPA1 channels and their importance in regulating vascular tone.
钙通透性非选择性阳离子通道,TRPA1(瞬态受体电位锚蛋白 1),是锚蛋白 TRP 亚家族的唯一成员。TRPA1 通道表达于神经元和非神经元细胞类型的质膜上,如血管内皮细胞。TRPA1 被亲电化合物激活,包括膳食分子,如异硫氰酸烯丙酯,芥末的衍生物。内源性的,该通道被认为是由活性氧及其代谢物激活的,如 4-羟基壬烯醛(4-HNE)。在血管系统中,TRPA1 通道的激活导致两种不同机制介导的血管舒张反应。首先,TRPA1 表达于血管的感觉神经中,激活后介导强效扩张剂降钙素基因相关肽(CGRP)的释放。其次,我们实验室的工作表明,TRPA1 仅在脑血管的内皮细胞中表达,其激活产生局部 Ca 信号,导致脑动脉扩张。在本章中,我们提供了 TRPA1 通道的生物物理和药理学特性及其在调节血管张力中的重要性的深入概述。