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突触膜泡运输中的磷酸肌醇

Phosphoinositides in membrane traffic at the synapse.

作者信息

Cremona O, De Camilli P

机构信息

Department of Medical Sciences, Università del Piemonte Orientale 'A. Avogadro', Via Solaroli 17, Italy.

出版信息

J Cell Sci. 2001 Mar;114(Pt 6):1041-52. doi: 10.1242/jcs.114.6.1041.

Abstract

Inositol phospholipids represent a minor fraction of membrane phospholipids; yet they play important regulatory functions in signaling pathways and membrane traffic. The phosphorylated inositol ring can act either as a precursor for soluble intracellular messengers or as a binding site for cytosolic or membrane proteins. Hence, phosphorylation-dephosphorylation of phosphoinositides represents a mechanism for regulation of recruitment to the membrane of coat proteins, cytoskeletal scaffolds or signaling complexes and for the regulation of membrane proteins. Recent work suggests that phosphoinositide metabolism has an important role in membrane traffic at the synapse. PtdIns(4,5)P2 generation is implicated in the secretion of at least a subset of neurotransmitters. Furthermore, PtdIns(4,5)P2 plays a role in the nucleation of clathrin coats and of an actin-based cytoskeletal scaffold at endocytic zones of synapses, and PtdIns(4,5)P2 dephosphorylation accompanies the release of newly formed vesicles from these interactions. Thus, the reversible phosphorylation of inositol phospholipids may be one of the mechanisms governing the timing and vectorial progression of synaptic vesicle membranes during their exocytic-endocytic cycle.

摘要

肌醇磷脂在膜磷脂中占比很小;然而,它们在信号通路和膜运输中发挥着重要的调节功能。磷酸化的肌醇环既可以作为可溶性细胞内信使的前体,也可以作为胞质或膜蛋白的结合位点。因此,磷酸肌醇的磷酸化-去磷酸化是一种调节机制,可调控包被蛋白、细胞骨架支架或信号复合物向膜的募集,以及调控膜蛋白。最近的研究表明,磷酸肌醇代谢在突触的膜运输中具有重要作用。磷脂酰肌醇-4,5-二磷酸(PtdIns(4,5)P2)的生成与至少一部分神经递质的分泌有关。此外,PtdIns(4,5)P2在突触内吞区域的网格蛋白包被和成肌动蛋白细胞骨架支架的成核过程中发挥作用,并且PtdIns(4,5)P2去磷酸化伴随着新形成的囊泡从这些相互作用中释放。因此,肌醇磷脂的可逆磷酸化可能是在突触小泡膜的胞吐-内吞循环中控制其时间和矢量进程的机制之一。

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