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本文引用的文献

1
Shedding light on the cell biology of extracellular vesicles.揭示细胞外囊泡的细胞生物学。
Nat Rev Mol Cell Biol. 2018 Apr;19(4):213-228. doi: 10.1038/nrm.2017.125. Epub 2018 Jan 17.
2
Annexin A4 and A6 induce membrane curvature and constriction during cell membrane repair.膜联蛋白 A4 和 A6 在细胞膜修复过程中诱导膜弯曲和收缩。
Nat Commun. 2017 Nov 20;8(1):1623. doi: 10.1038/s41467-017-01743-6.
3
Syntenin mediates SRC function in exosomal cell-to-cell communication.衔接蛋白在细胞外囊泡细胞间通讯中介导 SRC 功能。
Proc Natl Acad Sci U S A. 2017 Nov 21;114(47):12495-12500. doi: 10.1073/pnas.1713433114. Epub 2017 Nov 6.
4
Lipidomic and proteomic analysis of exosomes from mouse cortical collecting duct cells.小鼠皮质集合管细胞外泌体的脂质组学和蛋白质组学分析
FASEB J. 2017 Dec;31(12):5399-5408. doi: 10.1096/fj.201700417R. Epub 2017 Aug 16.
5
Comparative Characterization of Phosphatidic Acid Sensors and Their Localization during Frustrated Phagocytosis.磷脂酸传感器的比较特性及其在吞噬受阻过程中的定位
J Biol Chem. 2017 Mar 10;292(10):4266-4279. doi: 10.1074/jbc.M116.742346. Epub 2017 Jan 23.
6
Extracellular Vesicles: Unique Intercellular Delivery Vehicles.细胞外囊泡:独特的细胞间传递载体。
Trends Cell Biol. 2017 Mar;27(3):172-188. doi: 10.1016/j.tcb.2016.11.003. Epub 2016 Dec 13.
7
Cortactin enhances exosome secretion without altering cargo.皮层肌动蛋白增强外泌体分泌而不改变其内容物。
J Cell Biol. 2016 Jul 18;214(2):129-31. doi: 10.1083/jcb.201606131.
8
Cortactin promotes exosome secretion by controlling branched actin dynamics.皮层肌动蛋白通过控制分支状肌动蛋白动力学促进外泌体分泌。
J Cell Biol. 2016 Jul 18;214(2):197-213. doi: 10.1083/jcb.201601025. Epub 2016 Jul 11.
9
Frizzled 7 and PIP2 binding by syntenin PDZ2 domain supports Frizzled 7 trafficking and signalling.衔接蛋白 PDZ2 结构域与卷曲蛋白 7 及 PIP2 的结合支持卷曲蛋白 7 的运输和信号转导。
Nat Commun. 2016 Jul 8;7:12101. doi: 10.1038/ncomms12101.
10
Extracellular vesicles: masters of intercellular communication and potential clinical interventions.细胞外囊泡:细胞间通讯的掌控者及潜在的临床干预手段
J Clin Invest. 2016 Apr 1;126(4):1139-43. doi: 10.1172/JCI87316.

磷脂酶 D 和磷脂酸在外泌体的生物发生和货物装载中的作用。

Phospholipase D and phosphatidic acid in the biogenesis and cargo loading of extracellular vesicles.

机构信息

Centre de Recherche en Cancérologie de Marseille (CRCM), Equipe labellisée LIGUE 2018, Aix-Marseille Université, Marseille F-13284, France and Inserm U1068, Institut Paoli-Calmettes, and CNRS UMR7258, Marseille F-13009, France.

Centre de Recherche en Cancérologie de Marseille (CRCM), Equipe labellisée LIGUE 2018, Aix-Marseille Université, Marseille F-13284, France and Inserm U1068, Institut Paoli-Calmettes, and CNRS UMR7258, Marseille F-13009, France; Department of Human Genetics, University of Leuven, B-3000 Leuven, Belgium.

出版信息

J Lipid Res. 2018 Sep;59(9):1554-1560. doi: 10.1194/jlr.R083964. Epub 2018 May 31.

DOI:10.1194/jlr.R083964
PMID:29853529
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6121939/
Abstract

Extracellular vesicles released by viable cells (exosomes and microvesicles) have emerged as important organelles supporting cell-cell communication. Because of their potential therapeutic significance, important efforts are being made toward characterizing the contents of these vesicles and the mechanisms that govern their biogenesis. It has been recently demonstrated that the lipid modifying enzyme, phospholipase D (PLD)2, is involved in exosome production and acts downstream of the small GTPase, ARF6. This review aims to recapitulate our current knowledge of the role of PLD2 and its product, phosphatidic acid, in the biogenesis of exosomes and to propose hypotheses for further investigation of a possible central role of these molecules in the biology of these organelles.

摘要

细胞外囊泡(包括外泌体和微囊泡)是活细胞分泌的重要细胞器,在细胞间通讯中发挥重要作用。由于其具有潜在的治疗意义,因此人们正在努力对这些囊泡的内容物及其生物发生的机制进行描述。最近的研究表明,脂质修饰酶磷脂酶 D(PLD)2 参与外泌体的产生,并作用于小 GTP 酶 ARF6 的下游。本文旨在概述目前对 PLD2 及其产物磷酸脂酸在形成外泌体过程中的作用的认识,并提出进一步研究这些分子在这些细胞器生物学功能中可能具有核心作用的假说。