Shimizu Yuuki, Lambert Jonathan P, Nicholson Chad K, Kim Joshua J, Wolfson David W, Cho Hee Cheol, Husain Ahsan, Naqvi Nawazish, Chin Li-Shen, Li Lian, Calvert John W
Department of Surgery, Division of Cardiothoracic Surgery, Carlyle Fraser Heart Center, Emory University School of Medicine, Atlanta, GA, USA.
Division of Pediatric Cardiology, Department of Pediatrics, Emory University School of Medicine and Children's Healthcare of Atlanta, Atlanta, GA, USA; Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, GA, USA.
J Mol Cell Cardiol. 2016 Aug;97:56-66. doi: 10.1016/j.yjmcc.2016.04.008. Epub 2016 Apr 22.
Recent data indicates that DJ-1 plays a role in the cellular response to stress. Here, we aimed to examine the underlying molecular mechanisms mediating the actions of DJ-1 in the heart following myocardial ischemia-reperfusion (I/R) injury. In response to I/R injury, DJ-1 KO mice displayed increased areas of infarction and worsened left ventricular function when compared to WT mice, confirming a protective role for DJ-1 in the heart. In an effort to evaluate the potential mechanism(s) responsible for the increased injury in DJ-1 KO mice, we focused on SUMOylation, a post-translational modification process that regulates various aspects of protein function. DJ-1 KO hearts after I/R injury were found to display enhanced accumulation of SUMO-1 modified proteins and reduced SUMO-2/3 modified proteins. Further analysis, revealed that the protein expression of the de-SUMOylation enzyme SENP1 was reduced, whereas the expression of SENP5 was enhanced in DJ-1 KO hearts after I/R injury. Finally, DJ-1 KO hearts were found to display enhanced SUMO-1 modification of dynamin-related protein 1, excessive mitochondrial fission, and dysfunctional mitochondria. Our data demonstrates that the activation of DJ-1 in response to myocardial I/R injury protects the heart by regulating the SUMOylation status of Drp1 and attenuating excessive mitochondrial fission.
近期数据表明,DJ-1在细胞应激反应中发挥作用。在此,我们旨在研究心肌缺血再灌注(I/R)损伤后DJ-1在心脏中发挥作用的潜在分子机制。与野生型小鼠相比,对I/R损伤做出反应时,DJ-1基因敲除小鼠的梗死面积增加,左心室功能恶化,这证实了DJ-1在心脏中具有保护作用。为了评估导致DJ-1基因敲除小鼠损伤增加的潜在机制,我们聚焦于SUMO化,这是一种调节蛋白质功能各个方面的翻译后修饰过程。发现I/R损伤后的DJ-1基因敲除心脏中SUMO-1修饰蛋白的积累增强,而SUMO-2/3修饰蛋白减少。进一步分析表明,去SUMO化酶SENP1的蛋白表达降低,而I/R损伤后DJ-1基因敲除心脏中SENP5的表达增强。最后,发现DJ-1基因敲除心脏中发动蛋白相关蛋白1的SUMO-1修饰增强、线粒体过度分裂以及线粒体功能障碍。我们的数据表明,心肌I/R损伤后DJ-1的激活通过调节Drp1的SUMO化状态和减轻过度的线粒体分裂来保护心脏。