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本文引用的文献

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Autophagy as a promoter of longevity: insights from model organisms.自噬作为长寿的促进因素:来自模式生物的见解。
Nat Rev Mol Cell Biol. 2018 Sep;19(9):579-593. doi: 10.1038/s41580-018-0033-y.
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Classical and alternative roles for autophagy in lipid metabolism.自噬在脂质代谢中的经典作用和替代作用。
Curr Opin Lipidol. 2018 Jun;29(3):203-211. doi: 10.1097/MOL.0000000000000509.
3
Recent Insights into the Pathogenesis of Nonalcoholic Fatty Liver Disease.非酒精性脂肪性肝病发病机制的最新研究进展。
Annu Rev Pathol. 2018 Jan 24;13:321-350. doi: 10.1146/annurev-pathol-020117-043617.
4
Ethanol exposure inhibits hepatocyte lipophagy by inactivating the small guanosine triphosphatase Rab7.乙醇暴露通过使小GTP酶Rab7失活来抑制肝细胞脂质自噬。
Hepatol Commun. 2017 Mar 10;1(2):140-152. doi: 10.1002/hep4.1021. eCollection 2017 Apr.
5
Hepatic Lipophagy: New Insights into Autophagic Catabolism of Lipid Droplets in the Liver.肝脏脂质自噬:肝脏中脂滴自噬分解代谢的新见解
Hepatol Commun. 2017 Jul;1(5):359-369. doi: 10.1002/hep4.1056. Epub 2017 Jun 9.
6
ATGL Promotes Autophagy/Lipophagy via SIRT1 to Control Hepatic Lipid Droplet Catabolism.脂肪甘油三酯脂肪酶通过沉默调节蛋白1促进自噬/脂质自噬以控制肝脏脂滴分解代谢。
Cell Rep. 2017 Apr 4;19(1):1-9. doi: 10.1016/j.celrep.2017.03.026.
7
Store-Operated Ca Entry Controls Induction of Lipolysis and the Transcriptional Reprogramming to Lipid Metabolism.储存性钙内流调控脂解的诱导以及脂质代谢的转录重编程。
Cell Metab. 2017 Mar 7;25(3):698-712. doi: 10.1016/j.cmet.2016.12.021. Epub 2017 Jan 26.
8
A novel Rab10-EHBP1-EHD2 complex essential for the autophagic engulfment of lipid droplets.一种新型 Rab10-EHBP1-EHD2 复合物,对脂滴的自噬吞噬至关重要。
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9
COPI-TRAPPII activates Rab18 and regulates its lipid droplet association.衣被蛋白I-转运蛋白II激活Rab18并调节其与脂滴的结合。
EMBO J. 2017 Feb 15;36(4):441-457. doi: 10.15252/embj.201694866. Epub 2016 Dec 21.
10
Branched Chain Amino Acids Cause Liver Injury in Obese/Diabetic Mice by Promoting Adipocyte Lipolysis and Inhibiting Hepatic Autophagy.支链氨基酸通过促进脂肪细胞脂解和抑制肝脏自噬导致肥胖/糖尿病小鼠肝损伤。
EBioMedicine. 2016 Nov;13:157-167. doi: 10.1016/j.ebiom.2016.10.013. Epub 2016 Oct 11.

[脂肪自噬在脂质代谢调控中的作用及分子机制]

[Role of lipophagy in the regulation of lipid metabolism and the molecular mechanism].

作者信息

Shi Linna, Wang Ke, Deng Yudi, Wang Yingna, Zhu Shuangling, Yang Xushan, Liao Wenzhen

机构信息

Department of Nutrition, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.

School of Public Health, Southern Medical University, Guangzhou 510515, China.

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2019 Jul 30;39(7):867-874. doi: 10.12122/j.issn.1673-4254.2019.07.19.

DOI:10.12122/j.issn.1673-4254.2019.07.19
PMID:31340923
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6765557/
Abstract

Recent studies have discovered a selective autophagy-lipophagy, which can selectively identify and degrade lipids and plays an important role in regulating cellular lipid metabolism and maintaining intracellular lipid homeostasis. The process of lipophagy can be directly or indirectly regulated by genes, enzymes, transcriptional regulators and other factors. This review examines the role of lipophagy in reducing liver lipid content, regulating pancreatic lipid metabolism, and regulating adipose tissue differentiation, and summarizes the findings of the molecules (Rab GTPase, enzymes, ion channels, transcription factors, small molecular substances) involved in the regulation of lipophagy, which points to new directions for the treatment of diseases caused by lipid accumulation.

摘要

最近的研究发现了一种选择性自噬——脂质自噬,它能够选择性地识别并降解脂质,在调节细胞脂质代谢和维持细胞内脂质稳态方面发挥着重要作用。脂质自噬过程可受到基因、酶、转录调节因子及其他因素的直接或间接调控。本文综述了脂质自噬在降低肝脏脂质含量、调节胰腺脂质代谢以及调节脂肪组织分化中的作用,并总结了参与脂质自噬调节的分子(Rab GTP酶、酶、离子通道、转录因子、小分子物质)的研究结果,为治疗由脂质蓄积引起的疾病指明了新方向。