Technion Integrated Cancer Center, Department of Biochemistry, Ruth and Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa 31096, Israel.
Cells. 2021 Jul 26;10(8):1887. doi: 10.3390/cells10081887.
Calcium (Ca) signaling plays a dichotomous role in cellular biology, controlling cell survival and proliferation on the one hand and cellular toxicity and cell death on the other. Store-operated Ca entry (SOCE) by CRAC channels represents a major pathway for Ca entry in non-excitable cells. The CRAC channel has two key components, the endoplasmic reticulum Ca sensor stromal interaction molecule (STIM) and the plasma-membrane Ca channel Orai. Physical coupling between STIM and Orai opens the CRAC channel and the resulting Ca flux is regulated by a negative feedback mechanism of slow Ca dependent inactivation (SCDI). The identification of the SOCE-associated regulatory factor (SARAF) and investigations of its role in SCDI have led to new functional and molecular insights into how SOCE is controlled. In this review, we provide an overview of the functional and molecular mechanisms underlying SCDI and discuss how the interaction between SARAF, STIM1, and Orai1 shapes Ca signaling in cells.
钙(Ca)信号在细胞生物学中起着双重作用,一方面控制细胞的存活和增殖,另一方面控制细胞毒性和细胞死亡。由 CRAC 通道介导的储存操作钙内流(SOCE)是无兴奋性细胞中钙内流的主要途径。CRAC 通道有两个关键组成部分,内质网钙传感器基质相互作用分子(STIM)和质膜钙通道 Orai。STIM 和 Orai 之间的物理偶联打开 CRAC 通道,由此产生的 Ca 流受慢 Ca 依赖性失活(SCDI)的负反馈机制调节。SOCE 相关调节因子(SARAF)的鉴定及其在 SCDI 中的作用的研究,为 SOCE 如何被调控提供了新的功能和分子见解。在这篇综述中,我们概述了 SCDI 的功能和分子机制,并讨论了 SARAF、STIM1 和 Orai1 之间的相互作用如何塑造细胞中的 Ca 信号。