Finocchietto Paola V, Franco Maria C, Holod Silvia, Gonzalez Analia S, Converso Daniela P, Antico Arciuch Valeria G, Serra Maria P, Poderoso Juan J, Carreras Maria C
Laboratory of Oxygen Metabolism, University Hospital, 1120 Buenos Aires, Argentina.
Exp Biol Med (Maywood). 2009 Sep;234(9):1020-8. doi: 10.3181/0902-MR-81. Epub 2009 Jun 22.
Mitochondria are specialized organelles that control energy metabolism and also activate a multiplicity of pathways that modulate cell proliferation and mitochondrial biogenesis or, conversely, promote cell arrest and programmed cell death by a limited number of oxidative or nitrative reactions. Nitric oxide (NO) regulates oxygen uptake by reversible inhibition of cytochrome oxidase and the production of superoxide anion from the mitochondrial electron transfer chain. In this sense, NO produced by mtNOS will set the oxygen uptake level and contribute to oxidation-reduction reaction (redox)-dependent cell signaling. Modulation of translocation and activation of neuronal nitric oxide synthase (mtNOS activity) under different physiologic or pathologic conditions represents an adaptive response properly modulated to adjust mitochondria to different cell challenges.
线粒体是专门的细胞器,可控制能量代谢,并激活多种调节细胞增殖和线粒体生物合成的途径,或者相反,通过有限数量的氧化或硝化反应促进细胞停滞和程序性细胞死亡。一氧化氮(NO)通过可逆抑制细胞色素氧化酶来调节氧气摄取,并从线粒体电子传递链产生超氧阴离子。从这个意义上说,由线粒体一氧化氮合酶(mtNOS)产生的NO将设定氧气摄取水平,并有助于氧化还原反应(redox)依赖性细胞信号传导。在不同生理或病理条件下,神经元型一氧化氮合酶的易位和激活(mtNOS活性)的调节代表了一种适应性反应,可适当调节以调整线粒体以应对不同的细胞挑战。