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内质网-线粒体钙信号在肝脏代谢疾病中的作用。

Endoplasmic reticulum-mitochondria calcium signaling in hepatic metabolic diseases.

机构信息

INSERM UMR-1060, CarMeN Laboratory, Lyon 1 University, INRA U1397, F-69921 Oullins, France.

出版信息

Biochim Biophys Acta Mol Cell Res. 2017 Jun;1864(6):865-876. doi: 10.1016/j.bbamcr.2017.01.001. Epub 2017 Jan 4.

Abstract

The liver plays a central role in glucose homeostasis, and both metabolic inflexibility and insulin resistance predispose to the development of hepatic metabolic diseases. Mitochondria and endoplasmic reticulum (ER), which play a key role in the control of hepatic metabolism, also interact at contact points defined as mitochondria-associated membranes (MAM), in order to exchange metabolites and calcium (Ca) and regulate cellular homeostasis and signaling. Here, we overview the role of the liver in the control of glucose homeostasis, mainly focusing on the independent involvement of mitochondria, ER and Ca signaling in both healthy and pathological contexts. Then we focus on recent data highlighting MAM as important hubs for hormone and nutrient signaling in the liver, thus adapting mitochondria physiology and cellular metabolism to energy availability. Lastly, we discuss how chronic ER-mitochondria miscommunication could participate to hepatic metabolic diseases, pointing MAM interface as a potential therapeutic target for metabolic disorders. This article is part of a Special Issue entitled: ECS Meeting edited by Claus Heizmann, Joachim Krebs and Jacques Haiech.

摘要

肝脏在葡萄糖稳态中起着核心作用,代谢灵活性和胰岛素抵抗都会导致肝代谢疾病的发生。在线粒体和内质网(ER)在控制肝脏代谢中起着关键作用,它们也在定义为线粒体相关膜(MAM)的接触点相互作用,以交换代谢物和钙(Ca),并调节细胞内稳态和信号转导。在这里,我们综述了肝脏在控制葡萄糖稳态中的作用,主要集中在独立于线粒体、内质网和 Ca 信号在健康和病理环境中的作用。然后,我们重点介绍了最近的数据,这些数据强调了 MAM 作为肝脏中激素和营养信号的重要枢纽,从而使线粒体生理学和细胞代谢适应能量可用性。最后,我们讨论了慢性 ER-线粒体通信错误如何参与肝代谢疾病,并指出 MAM 界面是代谢紊乱的潜在治疗靶点。本文是由 Claus Heizmann、Joachim Krebs 和 Jacques Haiech 编辑的特刊“ECS Meeting”的一部分。

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