Wu Changgong, Yan Lin, Depre Christophe, Dhar Sunil K, Shen You-Tang, Sadoshima Junichi, Vatner Stephen F, Vatner Dorothy E
Department of Cell Biology and Molecular Medicine and Cardiovascular Research Institute, Univeristy of Medicine and Dentistry of New Jersey-New Jersey Medical School, Newark, New Jersey 07103, USA.
Am J Physiol Cell Physiol. 2009 Oct;297(4):C928-34. doi: 10.1152/ajpcell.00045.2009. Epub 2009 Jul 22.
Cytochrome c oxidase (COX) is composed of 13 subunits, of which COX I, II, and III are encoded by a mitochondrial gene. COX I and II function as the main catalytic components, but the function of COX III is unclear. Because myocardial ischemia affects mitochondrial oxidative metabolism, we hypothesized that COX activity and expression would be affected during postischemic cardiomyopathy. This hypothesis was tested in a monkey model following myocardial infarction (MI) and subsequent pacing-induced heart failure (HF). In this model, COX I protein expression was decreased threefold after MI and fourfold after HF (P < 0.05 vs. sham), whereas COX II expression remained unchanged. COX III protein expression increased 5-fold after MI and further increased 10-fold after HF compared with sham (P < 0.05 vs. sham). The physiological impact of COX III regulation was examined in vitro. Overexpression of COX III in mitochondria of HL-1 cells resulted in an 80% decrease in COX I, 60% decrease in global COX activity, 60% decrease in cell viability, and threefold increase in apoptosis (P < 0.05). Oxidative stress induced by H2O2 significantly (P < 0.05) increased COX III expression. H2O2 decreased cell viability by 47 +/- 3% upon overexpression of COX III, but only by 12 +/- 5% in control conditions (P < 0.05). We conclude that ischemic stress in vivo and oxidative stress in vitro lead to upregulation of COX III, followed by downregulation of COX I expression, impaired COX oxidative activity, and increased apoptosis. Therefore, upregulation of COX III may contribute to the increased susceptibility to apoptosis following MI and subsequent HF.
细胞色素c氧化酶(COX)由13个亚基组成,其中COX I、II和III由线粒体基因编码。COX I和II作为主要催化成分发挥作用,但COX III的功能尚不清楚。由于心肌缺血会影响线粒体氧化代谢,我们推测在缺血后心肌病期间COX活性和表达会受到影响。该假设在心肌梗死(MI)及随后起搏诱导的心力衰竭(HF)的猴子模型中进行了验证。在该模型中,MI后COX I蛋白表达降低了三倍,HF后降低了四倍(与假手术组相比,P < 0.05),而COX II表达保持不变。与假手术组相比,MI后COX III蛋白表达增加了5倍,HF后进一步增加了10倍(与假手术组相比,P < 0.05)。在体外研究了COX III调节的生理影响。HL-1细胞线粒体中COX III的过表达导致COX I降低80%,总体COX活性降低60%,细胞活力降低60%,凋亡增加三倍(P < 0.05)。H2O2诱导的氧化应激显著(P < 0.05)增加了COX III表达。COX III过表达时,H2O2使细胞活力降低47±3%,但在对照条件下仅降低12±5%(P < 0.05)。我们得出结论,体内缺血应激和体外氧化应激导致COX III上调,随后COX I表达下调、COX氧化活性受损及凋亡增加。因此,COX III上调可能导致MI及随后HF后凋亡易感性增加。