Piggott Christopher A, Jin Yishi
Neurobiology Section, Division of Biological Sciences, University of California, San Diego, San Diego, CA, United States.
Front Mol Neurosci. 2021 Jul 8;14:709390. doi: 10.3389/fnmol.2021.709390. eCollection 2021.
Contacts between the endoplasmic reticulum (ER) and plasma membrane (PM) contain specialized tethering proteins that bind both ER and PM membranes. In excitable cells, ER-PM contacts play an important role in calcium signaling and transferring lipids. Junctophilins are a conserved family of ER-PM tethering proteins. They are predominantly expressed in muscles and neurons and known to simultaneously bind both ER- and PM-localized ion channels. Since their discovery two decades ago, functional studies using junctophilin-deficient animals have provided a deep understanding of their roles in muscles and neurons, including excitation-contraction coupling, store-operated calcium entry (SOCE), and afterhyperpolarization (AHP). In this review, we highlight key findings from mouse, fly, and worm that support evolutionary conservation of junctophilins.
内质网(ER)与质膜(PM)之间的接触部位含有能同时结合内质网和质膜的特殊拴系蛋白。在可兴奋细胞中,内质网 - 质膜接触在钙信号传导和脂质转运中发挥重要作用。连接蛋白是一类保守的内质网 - 质膜拴系蛋白家族。它们主要在肌肉和神经元中表达,并且已知能同时结合内质网和质膜定位的离子通道。自二十年前被发现以来,使用连接蛋白缺陷动物进行的功能研究让我们深入了解了它们在肌肉和神经元中的作用,包括兴奋 - 收缩偶联、钙库操纵性钙内流(SOCE)以及超极化后电位(AHP)。在这篇综述中,我们重点介绍来自小鼠、果蝇和线虫的关键发现,这些发现支持连接蛋白在进化上的保守性。