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本文引用的文献

1
Mesenchymal Stem Cell-Derived Exosomes Ameliorated Diabetic Nephropathy by Autophagy Induction through the mTOR Signaling Pathway.间充质干细胞来源的外泌体通过mTOR信号通路诱导自噬改善糖尿病肾病
Cells. 2018 Nov 22;7(12):226. doi: 10.3390/cells7120226.
2
MicroRNA regulation of natural killer cell development and function in leukemia.微小 RNA 对白血病中自然杀伤细胞发育和功能的调控。
Mol Immunol. 2019 Nov;115:12-20. doi: 10.1016/j.molimm.2018.07.022. Epub 2018 Aug 9.
3
Inhibition of mitophagy decreases survival of Caenorhabditis elegans by increasing protein aggregation.抑制线粒体自噬会通过增加蛋白质聚集减少秀丽隐杆线虫的存活。
Mol Cell Biochem. 2019 Feb;452(1-2):123-131. doi: 10.1007/s11010-018-3418-5. Epub 2018 Aug 9.
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TSSC3 promotes autophagy via inactivating the Src-mediated PI3K/Akt/mTOR pathway to suppress tumorigenesis and metastasis in osteosarcoma, and predicts a favorable prognosis.TSSC3 通过抑制Src 介导的 PI3K/Akt/mTOR 通路促进自噬,从而抑制骨肉瘤的发生和转移,并预测预后良好。
J Exp Clin Cancer Res. 2018 Aug 9;37(1):188. doi: 10.1186/s13046-018-0856-6.
5
The interplay between exosomes and autophagy - partners in crime.外泌体与自噬的相互作用——共犯关系。
J Cell Sci. 2018 Aug 3;131(15):jcs215210. doi: 10.1242/jcs.215210.
6
Migration inhibition of water stress proteins from Nostoc commune Vauch. via activation of autophagy in DLD-1 cells.通过自噬作用激活 DLD-1 细胞,抑制发菜 Nostoc commune Vauch. 水胁迫蛋白的迁移。
Int J Biol Macromol. 2018 Nov;119:669-676. doi: 10.1016/j.ijbiomac.2018.07.188. Epub 2018 Jul 30.
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Autophagy enhances the replication of Peste des petits ruminants virus and inhibits caspase-dependent apoptosis in vitro.自噬增强了小反刍兽疫病毒的复制,并抑制了细胞凋亡。
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Autophagy activation contributes to lipid accumulation in tubular epithelial cells during kidney fibrosis.自噬激活在肾纤维化过程中促进肾小管上皮细胞脂质蓄积。
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9
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Knockdown of lncRNA AK139328 alleviates myocardial ischaemia/reperfusion injury in diabetic mice via modulating miR-204-3p and inhibiting autophagy.敲低长非编码 RNA AK139328 通过调节 miR-204-3p 抑制自噬减轻糖尿病小鼠心肌缺血/再灌注损伤。
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基于细胞外囊泡降解途径的自噬溶酶体途径。

Extracellular vesicles degradation pathway based autophagy lysosome pathway.

作者信息

Zheng Jun, Tan Jin, Miao Yu-Yang, Zhang Qiang

机构信息

Department of Geriatrics, Tianjin Medical University General Hospital, Tianjin Geriatrics Institute Tianjin, China.

Tianjin Medical University Tianjin, China.

出版信息

Am J Transl Res. 2019 Mar 15;11(3):1170-1183. eCollection 2019.

PMID:30972154
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6456539/
Abstract

As an ancient intracellular degradation pathway, the autophagy lysosome pathway exists in various cells continuously and stably and maintains cellular homeostasis by degrading damaged organelles and misfolded proteins that are prejudicial to cells. Extracellular vesicles (EVs) including microparticles and exosomes, are derived from varieties of mammalian tissue cells such as platelets, endothelial cells, cardiomyocytes. Through large quantity of active substances carried by EVs, EVs exert momentous biological functions. Recent researches have revealed the molecular mechanism of the interaction between extracellular vesicles and autophagy. In this review, we first elaborate that extracellular vesicles are identified and internalized by target cells by means of receptor-ligand. Since extracellular vesicles contain multiple functional molecules, we subsequently describe the process of intracellular autophagy pathway induced by extracellular vesicles, which activates autophagy-related pathways or delivers autophagy-associated molecules. Finally, we introduced the effects of extracellular vesicle-induced autophagy on extracellular vesicles and target cells respectively. In conclusion, this article integrates relevant theoretical knowledge of autophagy caused by extracellular vesicles and provides a new direction for the study of extracellular vesicles in the future.

摘要

作为一种古老的细胞内降解途径,自噬溶酶体途径持续稳定地存在于各种细胞中,并通过降解对细胞有害的受损细胞器和错误折叠的蛋白质来维持细胞内稳态。细胞外囊泡(EVs)包括微颗粒和外泌体,来源于多种哺乳动物组织细胞,如血小板、内皮细胞、心肌细胞。通过细胞外囊泡携带的大量活性物质,其发挥着重要的生物学功能。最近的研究揭示了细胞外囊泡与自噬之间相互作用的分子机制。在本综述中,我们首先阐述细胞外囊泡通过受体-配体被靶细胞识别并内化。由于细胞外囊泡含有多种功能分子,我们随后描述细胞外囊泡诱导细胞内自噬途径的过程,其激活自噬相关途径或传递自噬相关分子。最后,我们分别介绍了细胞外囊泡诱导的自噬对细胞外囊泡和靶细胞的影响。总之,本文整合了细胞外囊泡引起的自噬的相关理论知识,并为未来细胞外囊泡的研究提供了新方向。