Hill Bradford G, Darley-Usmar Victor M
Department of Pathology, Molecular and Cellular Division, University of Alabama at Birmingham, Biomedical Research Building II, 901 19th Street South, Birmingham, AL 35294-2180, USA.
Biochem J. 2008 Jun 1;412(2):e11-3. doi: 10.1042/BJ20080716.
Understanding the molecular mechanisms through which the heart could be protected from ischaemic injury is of major interest and offers a potential route for the development of new therapies. Recently, several studies have uncovered intriguing relationships between nitric oxide-induced protein thiol modifications and the cardioprotected phenotype. In a highly cited, seminal article published in the Biochemical Journal in 2006, Burwell and colleagues addressed this issue and provided direct evidence for S-nitrosation of complex I of the mitochondrial electron transport chain. These authors were the first to show increased S-nitrosation of mitochondrial proteins from hearts subjected to the cardioprotective process known as ischaemic preconditioning. This study has paved the way for further investigations that collectively reveal a potential link between the mitochondrial S-nitrosoproteome and ischaemic preconditioning.
了解心脏免受缺血性损伤的分子机制具有重大意义,并为开发新疗法提供了一条潜在途径。最近,多项研究揭示了一氧化氮诱导的蛋白质硫醇修饰与心脏保护表型之间的有趣关系。在2006年发表于《生物化学杂志》的一篇被高度引用的开创性文章中,Burwell及其同事探讨了这个问题,并为线粒体电子传递链复合体I的S-亚硝基化提供了直接证据。这些作者首次表明,经历了称为缺血预处理的心脏保护过程后,线粒体蛋白的S-亚硝基化增加。这项研究为进一步的研究铺平了道路,这些研究共同揭示了线粒体S-亚硝基化蛋白质组与缺血预处理之间的潜在联系。