Mitochondrial Nitric Oxide Synthase: A Masterpiece of Metabolic Adaptation, Cell Growth, Transformation, and Death

Author:

Finocchietto Paola V.1,Franco Maria C.1,Holod Silvia1,Gonzalez Analia S.1,Converso Daniela P.1,Arciuch Valeria G. Antico1,Serra Maria P.1,Poderoso Juan J.1,Carreras Maria C.1

Affiliation:

1. Laboratory of Oxygen Metabolism, University Hospital, Department of Clinical Biochemistry, School of Pharmacy and Biochemistry, and Department of Internal Medicine, School of Medicine, University of Buenos Aires, CONICET, 1120 Buenos Aires, Argentina

Abstract

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.

Publisher

SAGE Publications

Subject

General Biochemistry, Genetics and Molecular Biology

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