Laboratory of Signal Transduction, National Institute of Environmental Health Sciences-NIH, Department of Health and Human Services, Durham, North Carolina, USA.
Curr Top Membr. 2013;71:109-23. doi: 10.1016/B978-0-12-407870-3.00005-6.
Activation of phospholipase C results in release of intracellular Ca(2+) and activation of Ca(2+) entry. Plasma membrane Ca(2+) entry most commonly is signaled by the depletion of intracellular Ca(2+) stores, a mechanism referred to as capacitative calcium entry or store-operated calcium entry (SOCE). The major players in the SOCE pathway are a Ca(2+) sensor protein, STIM1, and a channel subunit, Orai1. STIM1 activates Orai channels by a mechanism that depends upon its colocalization with Orai at endoplasmic reticulum-plasma membrane junctions. Signaling proteins often occur in multiple forms with distinct properties and/or functions. Such forms arise by a number of mechanisms, including covalent modification, alternative splicing, and alternative translation initiation. This chapter summarizes and discusses recent work revealing alternative forms of STIM1 and Orai1, and the physiological consequences of these modified proteins.
磷脂酶 C 的激活导致细胞内 Ca(2+)的释放和 Ca(2+)内流的激活。质膜 Ca(2+)内流最常见的信号是细胞内 Ca(2+)储存的耗竭,这种机制被称为电容性钙内流或储存操纵性钙内流(SOCE)。SOCE 途径中的主要参与者是钙传感器蛋白 STIM1 和通道亚基 Orai1。STIM1 通过一种依赖于其与内质网-质膜连接处 Orai 共定位的机制激活 Orai 通道。信号蛋白通常以具有不同特性和/或功能的多种形式存在。这些形式的出现是通过多种机制产生的,包括共价修饰、选择性剪接和选择性翻译起始。本章总结和讨论了最近揭示 STIM1 和 Orai1 的替代形式以及这些修饰蛋白的生理后果的工作。