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自噬在正常和病变肝脏中的功能。

Functions of autophagy in normal and diseased liver.

机构信息

Department of Medicine; Marion Bessin Liver Research Center; Albert Einstein College of Medicine; Bronx, NY USA.

出版信息

Autophagy. 2013 Aug;9(8):1131-58. doi: 10.4161/auto.25063. Epub 2013 May 22.

DOI:10.4161/auto.25063
PMID:23774882
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3748187/
Abstract

Autophagy has emerged as a critical lysosomal pathway that maintains cell function and survival through the degradation of cellular components such as organelles and proteins. Investigations specifically employing the liver or hepatocytes as experimental models have contributed significantly to our current knowledge of autophagic regulation and function. The diverse cellular functions of autophagy, along with unique features of the liver and its principal cell type the hepatocyte, suggest that the liver is highly dependent on autophagy for both normal function and to prevent the development of disease states. However, instances have also been identified in which autophagy promotes pathological changes such as the development of hepatic fibrosis. Considerable evidence has accumulated that alterations in autophagy are an underlying mechanism of a number of common hepatic diseases including toxin-, drug- and ischemia/reperfusion-induced liver injury, fatty liver, viral hepatitis and hepatocellular carcinoma. This review summarizes recent advances in understanding the roles that autophagy plays in normal hepatic physiology and pathophysiology with the intent of furthering the development of autophagy-based therapies for human liver diseases.

摘要

自噬已成为一种关键的溶酶体途径,通过降解细胞器和蛋白质等细胞成分来维持细胞功能和生存。专门以肝脏或肝细胞为实验模型的研究,极大地促进了我们对自噬调控和功能的认识。自噬的多种细胞功能,以及肝脏及其主要细胞类型肝细胞的独特特征,表明肝脏对自噬的依赖性很强,不仅对正常功能如此,对预防疾病状态的发生也是如此。然而,也有一些例子表明,自噬会促进病理性变化,如肝纤维化的发展。大量证据表明,自噬的改变是许多常见肝脏疾病的潜在机制,包括毒素、药物和缺血/再灌注诱导的肝损伤、脂肪肝、病毒性肝炎和肝细胞癌。本综述总结了近年来对自噬在正常肝脏生理学和病理生理学中所起作用的理解进展,以期进一步开发基于自噬的人类肝脏疾病治疗方法。

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本文引用的文献

1
Transient activation of the PI3K-AKT pathway by hepatitis C virus to enhance viral entry.丙型肝炎病毒瞬时激活 PI3K-AKT 通路以增强病毒进入。
J Biol Chem. 2012 Dec 7;287(50):41922-30. doi: 10.1074/jbc.M112.414789. Epub 2012 Oct 24.
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Parkin and mitofusins reciprocally regulate mitophagy and mitochondrial spheroid formation.Parkin 和线粒体融合蛋白相互调节线粒体自噬和线粒体小球体的形成。
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Aging promotes the development of diet-induced murine steatohepatitis but not steatosis.衰老促进饮食诱导的小鼠脂肪性肝炎的发展,但不促进脂肪变性。
Hepatology. 2013 Mar;57(3):995-1004. doi: 10.1002/hep.26099. Epub 2013 Feb 12.
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Chronic overexpression of PNPLA3I148M in mouse liver causes hepatic steatosis.慢性过表达 PNPLA3I148M 于小鼠肝脏中可导致肝脂肪变性。
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The autophagy-related gene 14 (Atg14) is regulated by forkhead box O transcription factors and circadian rhythms and plays a critical role in hepatic autophagy and lipid metabolism.自噬相关基因 14(Atg14)受叉头框 O 转录因子和昼夜节律调节,在肝脏自噬和脂质代谢中发挥关键作用。
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Nrf2 redirects glucose and glutamine into anabolic pathways in metabolic reprogramming.Nrf2 将葡萄糖和谷氨酰胺重定向到代谢重编程中的合成代谢途径中。
Cancer Cell. 2012 Jul 10;22(1):66-79. doi: 10.1016/j.ccr.2012.05.016.
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Atg16L1, an essential factor for canonical autophagy, participates in hormone secretion from PC12 cells independently of autophagic activity.Atg16L1 是经典自噬所必需的因素,它独立于自噬活性参与 PC12 细胞的激素分泌。
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