Nemoto S, Takeda K, Yu Z X, Ferrans V J, Finkel T
Laboratory of Molecular Biology, National Heart Lung and Blood Institute, NIH, Bethesda, Maryland 20892, USA.
Mol Cell Biol. 2000 Oct;20(19):7311-8. doi: 10.1128/MCB.20.19.7311-7318.2000.
Leakage of mitochondrial oxidants contributes to a variety of harmful conditions ranging from neurodegenerative diseases to cellular senescence. We describe here, however, a physiological and heretofore unrecognized role for mitochondrial oxidant release. Mitochondrial metabolism of pyruvate is demonstrated to activate the c-Jun N-terminal kinase (JNK). This metabolite-induced rise in cytosolic JNK1 activity is shown to be triggered by increased release of mitochondrial H(2)O(2). We further demonstrate that in turn, the redox-dependent activation of JNK1 feeds back and inhibits the activity of the metabolic enzymes glycogen synthase kinase 3beta and glycogen synthase. As such, these results demonstrate a novel metabolic regulatory pathway activated by mitochondrial oxidants. In addition, they suggest that although chronic oxidant production may have deleterious effects, mitochondrial oxidants can also function acutely as signaling molecules to provide communication between the mitochondria and the cytosol.
线粒体氧化剂的泄漏会导致从神经退行性疾病到细胞衰老等多种有害状况。然而,我们在此描述了线粒体氧化剂释放的一种生理作用,且此作用此前未被认识到。丙酮酸的线粒体代谢被证明可激活c-Jun氨基末端激酶(JNK)。这种代谢产物诱导的胞质JNK1活性升高被证明是由线粒体H₂O₂释放增加所触发的。我们进一步证明,反过来,JNK1的氧化还原依赖性激活会反馈并抑制代谢酶糖原合酶激酶3β和糖原合酶的活性。因此,这些结果证明了一种由线粒体氧化剂激活的新型代谢调节途径。此外,它们表明,尽管慢性氧化剂产生可能具有有害影响,但线粒体氧化剂也可作为信号分子发挥急性作用,以实现线粒体与胞质之间的通信。