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Am J Physiol Cell Physiol 292: C52-C58, 2007. First published August 30, 2006; doi:10.1152/ajpcell.00208.2006
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INVITED REVIEWS

Mechanisms of mitochondrial response to variations in energy demand in eukaryotic cells

Anne Devin and Michel Rigoulet

Institut de Biochimie et Génétique Cellulaire du Centre National de la Recherche Scientifique, Unité Mixte Recherche 5095, Université Victor Segalen Bordeaux, Bordeaux cedex, France

This review focuses on the different mechanisms involved in the adjustment of mitochondrial ATP production to cellular energy demand. The oxidative phosphorylation steady state at constant mitochondrial enzyme content can vary in response to energy demand. However, such an adaptation is tightly linked to a modification in both oxidative phosphorylation yield and phosphate potential and is obviously very limited in eukaryotic cells. We describe the three main mechanisms involved in mitochondrial response to energy demand. In heart cells, a short-term adjustment can be reached mainly through metabolic signaling via phosphotransfer networks by the compartmentalized energy transfer and signal transmission. In such a complex regulatory mechanism, Ca2+ signaling participates in activation of matricial dehydrogenases as well as mitochondrial ATP synthase. These processes allow a large increase in ATP production rate without an important modification in thermodynamic forces. For a long-term adaptation, two main mechanisms are involved: modulation of the mitochondrial enzyme content as a function of energy demand and/or kinetic regulation by covalent modifications (phosphorylations) of some respiratory chain complex subunits. Regardless of the mechanism involved (kinetic regulation by covalent modification or adjustment of mitochondrial enzyme content), the cAMP signaling pathway plays a major role in molecular signaling, leading to the mitochondrial response. We discuss the energetic advantages of these mechanisms.

yeast; C6 glioma cells; muscle; kinetic regulation



Address for reprint requests and other correspondence: M. Rigoulet, IBGC du CNRS, UMR 5095, Université Victor Segalen Bordeaux 2, 1 rue Camille Saint Saëns, 33077 Bordeaux cedex, France (e-mail: michel.rigoulet{at}ibgc.u-bordeaux2.fr)




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