Zhang Weihua, Xu Changqing
Department of Pathophysiology, Harbin Medical University, Harbin 150086, China; Bio-pharmaceutical Key Laboratory of Heilongjiang Province, Harbin Medical University, Harbin 150086, China.
Pathophysiology. 2009 Oct;16(4):317-23. doi: 10.1016/j.pathophys.2009.02.013. Epub 2009 Mar 24.
Calcium ion is the first identified endogenous substance to function as both a first and second messenger via the stimulation of an extracellular calcium sensing receptor (CaR). CaR is a seven transmembrane G-protein-coupled receptor, which activates intracellular effectors, for example, it causes inositol phosphate (IP) accumulation to increase the release of intracellular calcium. Furthermore, more and more evidence shows that CaR is related to mediating the cellular functions in various cells.
Since 2003, CaR has been detected to be functionally expressed in the atria and ventricle of the rat hearts. Recently, increasing evidence suggests that CaR has been involved in apoptosis in the ischemia/reperfusion heart through caspase-3-Cytochrome c and FasL/Fas and endoplasmic reticulum stress pathways and also involved in cardiac hypertrophy-induced by AngII through CaN pathway in neonatal rat cardiomyocytes.
These results suggested that CaR in cardiac tissue might have a physiological and pathophysiological role in heart disease. This review revealed CaR's structure and function and emphasized the role of CaR in the cardiac tissues.
钙离子是首个被鉴定出的内源性物质,它通过刺激细胞外钙敏感受体(CaR)发挥第一信使和第二信使的功能。CaR是一种七跨膜G蛋白偶联受体,可激活细胞内效应器,例如,它会导致肌醇磷酸(IP)积累,从而增加细胞内钙的释放。此外,越来越多的证据表明,CaR与介导各种细胞的细胞功能有关。
自2003年以来,已检测到CaR在大鼠心脏的心房和心室中功能性表达。最近,越来越多的证据表明,CaR通过半胱天冬酶-3-细胞色素c和FasL/Fas以及内质网应激途径参与缺血/再灌注心脏的细胞凋亡,并且在新生大鼠心肌细胞中通过钙调神经磷酸酶途径参与血管紧张素II诱导的心肌肥大。
这些结果表明,心脏组织中的CaR可能在心脏病中具有生理和病理生理作用。本综述揭示了CaR的结构和功能,并强调了CaR在心脏组织中的作用。