Li Chenlu, Qian Tiantian, He Ruyue, Wan Chun, Liu Yinghui, Yu Haijia
Jiangsu Key Laboratory for Molecular and Medical Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing, China.
Department of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder, CO, United States.
Front Cell Dev Biol. 2021 Feb 4;9:627700. doi: 10.3389/fcell.2021.627700. eCollection 2021.
The endoplasmic reticulum (ER) forms direct membrane contact sites with the plasma membrane (PM) in eukaryotic cells. These ER-PM contact sites play essential roles in lipid homeostasis, ion dynamics, and cell signaling, which are carried out by protein-protein or protein-lipid interactions. Distinct tethering factors dynamically control the architecture of ER-PM junctions in response to intracellular signals or external stimuli. The physiological roles of ER-PM contact sites are dependent on a variety of regulators that individually or cooperatively perform functions in diverse cellular processes. This review focuses on proteins functioning at ER-PM contact sites and highlights the recent progress in their mechanisms and physiological roles.
在内真核细胞中,内质网(ER)与质膜(PM)形成直接的膜接触位点。这些内质网 - 质膜接触位点在脂质稳态、离子动态平衡和细胞信号传导中发挥着重要作用,这些作用是通过蛋白质 - 蛋白质或蛋白质 - 脂质相互作用来实现的。不同的拴系因子会根据细胞内信号或外部刺激动态控制内质网 - 质膜连接的结构。内质网 - 质膜接触位点的生理作用依赖于多种调节因子,这些调节因子在不同的细胞过程中单独或协同发挥功能。本综述重点关注在内质网 - 质膜接触位点发挥作用的蛋白质,并强调了它们的机制和生理作用方面的最新进展。