Cahalan Michael D
Department of Physiology and Biophysics and Institute for Immunology, University of California, Irvine, CA 92697-4561, USA.
Nat Cell Biol. 2009 Jun;11(6):669-77. doi: 10.1038/ncb0609-669.
Calcium influx through plasma membrane store-operated Ca(2+) (SOC) channels is triggered when the endoplasmic reticulum (ER) Ca(2+) store is depleted - a homeostatic Ca(2+) signalling mechanism that remained enigmatic for more than two decades. RNA-interference (RNAi) screening and molecular and cellular physiological analysis recently identified STIM1 as the mechanistic 'missing link' between the ER and the plasma membrane. STIM proteins sense the depletion of Ca(2+) from the ER, oligomerize, translocate to junctions adjacent to the plasma membrane, organize Orai or TRPC (transient receptor potential cation) channels into clusters and open these channels to bring about SOC entry.
当内质网(ER)钙库耗尽时,质膜储存-操纵性钙(2+)(SOC)通道介导的钙内流被触发,这是一种二十多年来一直令人费解的钙稳态信号机制。RNA干扰(RNAi)筛选以及分子和细胞生理学分析最近确定,基质相互作用分子1(STIM1)是内质网与质膜之间机制上的“缺失环节”。STIM蛋白感知内质网中钙的耗尽,发生寡聚化,转位至与质膜相邻的连接处,将奥拉帕尼或瞬时受体电位阳离子(TRPC)通道组织成簇并打开这些通道,从而实现SOC内流。