Takeshima Hiroshi
Department of Medical Chemistry, Tohoku University Graduate School of Medicine, Seiryo-machi, Sendai, Miyagi, Japan.
Nihon Yakurigaku Zasshi. 2003 Apr;121(4):203-10. doi: 10.1254/fpj.121.203.
In excitable cell types, activation of cell-surface Ca(2+) channels triggers Ca(2+) release from the endplasmic or sarcoplasmic reticulum (ER/SR). This Ca(2+) signal amplification, termed Ca(2+)-induced or voltage-induced Ca(2+) release (CICR/VICR), requires the ryanodine receptor as an intracellular Ca(2+) channel, which is predominantly localized in the junctional membrane complex between the plasma membrane and the ER/SR. Junctophilin is an ER/SR membrane protein that contributes to the formation of the junctional membrane structure. Ryanodine receptor and junctophilin subtypes are derived from distinct genes and show different tissue-specific expression. Recent gene-knockout studies have defined physiological functions of both Ca(2+) release via ryanodine receptors and junctional membrane structures constituted by junctophilins in excitable cells. Moreover, several human genetic diseases are caused by mutations at the ryanodine receptor and junctophilin subtype genes.
在可兴奋细胞类型中,细胞表面钙离子通道的激活会触发内质网或肌浆网(ER/SR)释放钙离子。这种钙离子信号放大,称为钙诱导或电压诱导的钙离子释放(CICR/VICR),需要兰尼碱受体作为细胞内钙离子通道,该受体主要定位于质膜与ER/SR之间的连接膜复合体中。连接蛋白是一种ER/SR膜蛋白,有助于连接膜结构的形成。兰尼碱受体和连接蛋白亚型源自不同基因,并表现出不同的组织特异性表达。最近的基因敲除研究已经明确了通过兰尼碱受体释放钙离子以及由连接蛋白构成的连接膜结构在可兴奋细胞中的生理功能。此外,几种人类遗传疾病是由兰尼碱受体和连接蛋白亚型基因的突变引起的。