Goto Kenichi, Kitazono Takanari
Department of Health Sciences, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Department of Medicine and Clinical Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Front Physiol. 2021 Sep 20;12:728979. doi: 10.3389/fphys.2021.728979. eCollection 2021.
Vascular endothelial cells regulate arterial tone through the release of nitric oxide and other diffusible factors such as prostacyclin and endothelium derived hyperpolarizing factors. Alongside these diffusible factors, contact-mediated electrical propagation from endothelial cells to smooth muscle cells myoendothelial gap junctions, termed endothelium-dependent hyperpolarization (EDH), plays a critical role in endothelium-dependent vasodilation in certain vascular beds. A rise in intracellular Ca concentration in endothelial cells is a prerequisite for both the production of diffusible factors and the generation of EDH, and Ca influx through the endothelial transient receptor potential vanilloid 4 (TRPV4) ion channel, a nonselective cation channel of the TRP family, plays a critical role in this process in various vascular beds. Emerging evidence suggests that the dysregulation of endothelial TRPV4 channels underpins endothelial dysfunction associated with cardiovascular disease (CVD) risk factors, including hypertension, obesity, diabetes, and aging. Because endothelial dysfunction is a precursor to CVD, a better understanding of the mechanisms underlying impaired TRPV4 channels could lead to novel therapeutic strategies for CVD prevention. In this mini review, we present the current knowledge of the pathophysiological changes in endothelial TRPV4 channels associated with CVD risk factors, and then explore the underlying mechanisms involved.
血管内皮细胞通过释放一氧化氮以及其他可扩散因子(如前列环素和内皮衍生超极化因子)来调节动脉张力。除了这些可扩散因子外,内皮细胞与平滑肌细胞之间通过肌内皮间隙连接进行的接触介导的电传导,即内皮依赖性超极化(EDH),在某些血管床的内皮依赖性血管舒张中起关键作用。内皮细胞内钙离子浓度升高是可扩散因子产生和EDH生成的先决条件,而通过内皮瞬时受体电位香草酸亚型4(TRPV4)离子通道的钙离子内流在这一过程中起着关键作用,TRPV4是TRP家族的一种非选择性阳离子通道,在各种血管床中均如此。新出现的证据表明,内皮TRPV4通道的失调是与心血管疾病(CVD)风险因素(包括高血压、肥胖、糖尿病和衰老)相关的内皮功能障碍的基础。由于内皮功能障碍是CVD的先兆,因此更好地了解TRPV4通道受损的机制可能会带来预防CVD的新治疗策略。在本综述中,我们介绍了与CVD风险因素相关的内皮TRPV4通道病理生理变化的现有知识,然后探讨其中涉及的潜在机制。