Department of Gastroenterology, Xinqiao Hospital, Army Medical University, Chongqing, China.
Department of Gastroenterology, Xinqiao Hospital, Army Medical University, Chongqing, China.
Life Sci. 2018 Sep 15;209:217-227. doi: 10.1016/j.lfs.2018.08.016. Epub 2018 Aug 8.
Ca-sensing receptor (CaSR), a member of G protein-coupled receptor family, is widely expressed in the vascular system, including perivascular neurons, vascular endothelial cells (VECs) and vascular smooth muscle cells (VSMCs). When stimulated, CaSR can further increase the cytosolic Ca concentration ([Ca]) in two ways: intracellular Ca release from endo/sarcoplasmic reticulum (ER/SR) and extracellular Ca entry through Ca-permeable cation channels. In endothelium, increased Ca subsequently activate nitric oxide synthase (NOS) and intermediate conductance Ca-activated K channels (IKCa), resulting in vasodilation through NOS-mediated NO release or membrane hyperpolarization. In VSMCs, CaSR-induced intracellular Ca increase causes blood vessel constriction. CaSR activation predominantly induces vasorelaxation of whole vascular tissues through VECs-dependent mechanisms; however, CaSR-induced Ca signaling in VSMCs may play a braking role in CaSR-mediated vasorelaxation. Emerging evidence reveals the importance of CaSR in the regulation of vascular tone and blood pressure. Here, we summarized recent advances in CaSR-mediated vascular reaction and the underlying mechanisms in different species, including humans. In addition, several studies have demonstrated that CaSR dysfunction may be associated with some fatal vascular diseases, such as pulmonary arterial hypertension, primary hypertension, diabetes, acute myocardial infarction and vascular calcification. With the advance of studies on CaSR in vascular health and disease, it is expected positive modulators or negative modulators of CaSR used for the treatment of specific diseases may be promising therapeutic options for the prevention and/or treatment of vascular diseases.
钙敏感受体(CaSR)是 G 蛋白偶联受体家族的成员,广泛表达于血管系统,包括血管周围神经元、血管内皮细胞(VECs)和血管平滑肌细胞(VSMCs)。当受到刺激时,CaSR 可以通过两种方式进一步增加细胞浆内钙离子浓度([Ca]):从内质网/肌浆网(ER/SR)内释放细胞内钙和通过钙通透阳离子通道从细胞外摄取钙。在内皮细胞中,增加的钙随后激活一氧化氮合酶(NOS)和中电导钙激活钾通道(IKCa),导致通过 NOS 介导的一氧化氮释放或细胞膜超极化引起血管舒张。在 VSMCs 中,CaSR 诱导的细胞内钙增加导致血管收缩。CaSR 激活主要通过 VECs 依赖性机制引起整个血管组织的血管舒张;然而,CaSR 诱导的 VSMCs 内钙信号可能在 CaSR 介导的血管舒张中起制动作用。新出现的证据表明 CaSR 在血管张力和血压调节中的重要性。在这里,我们总结了 CaSR 介导的血管反应及其在不同物种(包括人类)中的潜在机制的最新进展。此外,一些研究表明 CaSR 功能障碍可能与某些致命的血管疾病有关,如肺动脉高压、原发性高血压、糖尿病、急性心肌梗死和血管钙化。随着对 CaSR 在血管健康和疾病中的研究进展,CaSR 的正调节剂或负调节剂有望成为治疗特定疾病的有前途的治疗选择,可用于预防和/或治疗血管疾病。