Handhle Ahmed, Ormonde Chloe E, Thomas N Lowri, Bralesford Catherine, Williams Alan J, Lai F Anthony, Zissimopoulos Spyros
Sir Geraint Evans Wales Heart Research Institute, School of Medicine, Cardiff University, Cardiff CF14 4XN, UK.
Medical Biochemistry Department, Faculty of Medicine, Mansoura University, Mansoura 35516, Egypt.
J Cell Sci. 2016 Nov 1;129(21):3983-3988. doi: 10.1242/jcs.191643. Epub 2016 Sep 8.
Cardiac muscle contraction requires sarcoplasmic reticulum (SR) Ca release mediated by the quaternary complex comprising the ryanodine receptor 2 (RyR2), calsequestrin 2 (CSQ2), junctin (encoded by ASPH) and triadin. Here, we demonstrate that a direct interaction exists between RyR2 and CSQ2. Topologically, CSQ2 binding occurs at the first luminal loop of RyR2. Co-expression of RyR2 and CSQ2 in a human cell line devoid of the other quaternary complex proteins results in altered Ca-release dynamics compared to cells expressing RyR2 only. These findings provide a new perspective for understanding the SR luminal Ca sensor and its involvement in cardiac physiology and disease.
心肌收缩需要由包含兰尼碱受体2(RyR2)、肌集钙蛋白2(CSQ2)、连接蛋白(由ASPH编码)和三联蛋白的四聚体复合物介导的肌浆网(SR)钙释放。在此,我们证明RyR2和CSQ2之间存在直接相互作用。从拓扑结构上看,CSQ2结合发生在RyR2的第一个腔内环。与仅表达RyR2的细胞相比,在缺乏其他四聚体复合物蛋白的人类细胞系中共表达RyR2和CSQ2会导致钙释放动力学改变。这些发现为理解SR腔内钙传感器及其在心脏生理学和疾病中的作用提供了新的视角。