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细胞器间膜微区:钙信号和细胞凋亡调控中的动态平台。

Interorganellar membrane microdomains: dynamic platforms in the control of calcium signaling and apoptosis.

机构信息

Department of Genetics and Tumor Cell Biology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.

出版信息

Cells. 2013 Aug 2;2(3):574-90. doi: 10.3390/cells2030574.

Abstract

The dynamic interplay among intracellular organelles occurs at specific membrane tethering sites, where two organellar membranes come in close apposition but do not fuse. Such membrane microdomains allow for rapid and efficient interorganelle communication that contributes to the maintenance of cell physiology. Pathological conditions that interfere with the proper composition, number, and physical vicinity of the apposing membranes initiate a cascade of events resulting in cell death. Membrane contact sites have now been identified that tether the extensive network of the endoplasmic reticulum (ER) membranes with the mitochondria, the plasma membrane (PM), the Golgi and the endosomes/lysosomes. Thus far, the most extensively studied are the MAMs, or mitochondria associated ER membranes, and the ER-PM junctions that share functional properties and crosstalk to one another. Specific molecular components that define these microdomains have been shown to promote the interaction in trans between these intracellular compartments and the transfer or exchange of Ca2+ ions, lipids, and metabolic signaling molecules that determine the fate of the cell.

摘要

细胞内细胞器之间的动态相互作用发生在特定的膜连接位点,在这些位点上,两个细胞器膜紧密相邻但不融合。这种膜微区允许快速有效地进行细胞器间的通讯,有助于维持细胞的生理功能。干扰相邻膜适当组成、数量和物理接近度的病理条件会引发一系列事件,导致细胞死亡。现在已经确定了一些膜接触位点,将内质网 (ER) 膜的广泛网络与线粒体、质膜 (PM)、高尔基体和内体/溶酶体连接起来。到目前为止,研究最多的是 MAMs(线粒体相关内质网)和 ER-PM 连接点,它们具有共同的功能特性并相互交流。已经表明,定义这些微区的特定分子成分促进了这些细胞内隔室之间的相互作用以及 Ca2+ 离子、脂质和代谢信号分子的转移或交换,这些分子决定了细胞的命运。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd0a/3972666/458aac668aed/cells-02-00574-g001.jpg

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