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外源性基因转导诱导型 2 型异柠檬酸脱氢酶模拟缺血预处理保护作用。

Exogenous Gene Transmission of Isocitrate Dehydrogenase 2 Mimics Ischemic Preconditioning Protection.

机构信息

Department of Biology, Indiana University-Purdue University, Indianapolis, Indianapolis, Indiana.

Research Division, Richard L. Roudebush Veterans Affairs Medical Center, Indianapolis, Indiana.

出版信息

J Am Soc Nephrol. 2018 Apr;29(4):1154-1164. doi: 10.1681/ASN.2017060675. Epub 2018 Jan 25.

Abstract

Ischemic preconditioning confers organ-wide protection against subsequent ischemic stress. A substantial body of evidence underscores the importance of mitochondria adaptation as a critical component of cell protection from ischemia. To identify changes in mitochondria protein expression in response to ischemic preconditioning, we isolated mitochondria from ischemic preconditioned kidneys and sham-treated kidneys as a basis for comparison. The proteomic screen identified highly upregulated proteins, including NADP+-dependent isocitrate dehydrogenase 2 (IDH2), and we confirmed the ability of this protein to confer cellular protection from injury in murine S3 proximal tubule cells subjected to hypoxia. To further evaluate the role of IDH2 in cell protection, we performed detailed analysis of the effects of gene delivery on kidney susceptibility to ischemia-reperfusion injury. Gene delivery of before injury attenuated the injury-induced rise in serum creatinine (<0.05) observed in controls and increased the mitochondria membrane potential (<0.05), maximal respiratory capacity (<0.05), and intracellular ATP levels (<0.05) above those in controls. This communication shows that gene delivery of can confer organ-wide protection against subsequent ischemia-reperfusion injury and mimics ischemic preconditioning.

摘要

缺血预处理赋予器官对后续缺血应激的广泛保护作用。大量证据强调了线粒体适应作为细胞免受缺血损伤的关键组成部分的重要性。为了鉴定对缺血预处理的反应中,线粒体蛋白表达的变化,我们从缺血预处理的肾脏和假处理的肾脏中分离出线粒体,作为比较的基础。蛋白质组学筛选鉴定出高度上调的蛋白质,包括 NADP+-依赖性异柠檬酸脱氢酶 2(IDH2),并且我们证实了这种蛋白质在缺氧条件下的小鼠 S3 近端肾小管细胞中赋予细胞损伤保护的能力。为了进一步评估 IDH2 在细胞保护中的作用,我们对基因传递对肾脏对缺血再灌注损伤易感性的影响进行了详细分析。在损伤前进行基因传递,可以减轻对照组中观察到的损伤诱导的血清肌酐升高(<0.05),并增加线粒体膜电位(<0.05)、最大呼吸能力(<0.05)和细胞内 ATP 水平(<0.05)高于对照组。本研究表明,基因传递可以赋予器官对后续缺血再灌注损伤的广泛保护作用,并模拟缺血预处理。

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