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内质网-质膜连接点的组装:在 SOCE 和 TRPC1 调节中的关键决定因素。

Assembly of ER-PM Junctions: A Critical Determinant in the Regulation of SOCE and TRPC1.

机构信息

Secretory Physiology Section, Molecular Physiology and Therapeutics Branch, NIDCR, NIH, Bethesda, MD, USA.

出版信息

Adv Exp Med Biol. 2017;981:253-276. doi: 10.1007/978-3-319-55858-5_11.

Abstract

Store-operated calcium entry (SOCE), a unique plasma membrane Ca entry mechanism, is activated when ER-[Ca] is decreased. SOCE is mediated via the primary channel, Orai1, as well as others such as TRPC1. STIM1 and STIM2 are ER-Ca sensor proteins that regulate Orai1 and TRPC1. SOCE requires assembly of STIM proteins with the plasma membrane channels which occurs within distinct regions in the cell that have been termed as endoplasmic reticulum (ER)-plasma membrane (PM) junctions. The PM and ER are in close proximity to each other within this region, which allows STIM1 in the ER to interact with and activate either Orai1 or TRPC1 in the plasma membrane. Activation and regulation of SOCE involves dynamic assembly of various components that are involved in mediating Ca entry as well as those that determine the formation and stabilization of the junctions. These components include proteins in the cytosol, ER and PM, as well as lipids in the PM. Recent studies have also suggested that SOCE and its components are compartmentalized within ER-PM junctions and that this process might require remodeling of the plasma membrane lipids and reorganization of structural and scaffolding proteins. Such compartmentalization leads to the generation of spatially- and temporally-controlled Casignals that are critical for regulating many downstream cellular functions.

摘要

钙库操纵性钙内流(SOCE)是一种独特的质膜钙内流机制,当内质网 [Ca] 减少时被激活。SOCE 通过主要通道 Orai1 以及其他通道如 TRPC1 介导。STIM1 和 STIM2 是内质网 Ca 传感器蛋白,调节 Orai1 和 TRPC1。SOCE 需要 STIM 蛋白与质膜通道组装,这在内质网 (ER)-质膜 (PM) 连接点的不同区域中发生。在这个区域中,PM 和 ER 彼此非常接近,这允许 ER 中的 STIM1 与质膜中的 Orai1 或 TRPC1 相互作用并激活它们。SOCE 的激活和调节涉及参与介导钙内流的各种组件的动态组装,以及决定连接点形成和稳定的组件。这些组件包括细胞质、ER 和 PM 中的蛋白质以及 PM 中的脂质。最近的研究还表明,SOCE 及其组件在 ER-PM 连接点中被分隔开,并且该过程可能需要质膜脂质的重塑和结构和支架蛋白的重组。这种分隔导致产生空间和时间控制的 Casignals,这对于调节许多下游细胞功能至关重要。

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