FEBS Letters | |
New molecular aspects of regulation of mitochondrial activity by fenofibrate and fasting | |
Wrutniak-Cabello, Chantal3  Rodier, Anne3  Daury, Laetitia3  Cabello, Gérard3  Pineau, Thierry2  Rochard, Pierrick3  Dauça, Michel1  Casas, François3  | |
[1] Laboratoire de Biologie Cellulaire du Développement, EA 2402 ‘Proliférateurs de Peroxysomes’, Université Henri Poincaré-Nancy I, Faculté des Sciences, P.O. Box 239, 54506 Vandoeuvre-lès-Nancy Cedex, France;Laboratoire de Pharmacologie Toxicologie, Institut National de la Recherche Agronomique (INRA), 180 Chemin de Tournefeuille, P.O. Box 3, 31931 Toulouse Cedex 9, France;UMR Différenciation Cellulaire et Croissance (INRA-UMII-ENSAM), Unité d'Endocrinologie Cellulaire, Institut National de la Recherche Agronomique (INRA), place Viala, 34060 Montpellier Cedex 1, France | |
关键词: Mitochondrion; Fibrate; Fasting; Mitochondrial T3 receptor; Peroxisome proliferator activated receptor; | |
DOI : 10.1016/S0014-5793(00)02023-8 | |
学科分类:生物化学/生物物理 | |
来源: John Wiley & Sons Ltd. | |
【 摘 要 】
Fenofibrate and fasting are known to regulate several genes involved in lipid metabolism in a similar way. In this study measuring several mitochondrial enzyme activities, we demonstrate that, in contrast to citrate synthase and complex II, cytochrome c oxidase (COX) is a specific target of these two treatments. In mouse liver organelles, Western blot experiments indicated that mitochondrial levels of p43, a mitochondrial T3 receptor, and mitochondrial peroxisome proliferator activated receptor (mt-PPAR), previously described as a dimeric partner of p43 in the organelle, are increased by both fenofibrate and fasting. In addition, in PPARα-deficient mice, this influence was abolished for mt-PPAR but not for p43, whereas the increase in COX activity was not altered. These data indicate that: (1) PPARα is involved in specific regulation of mt-PPAR expression by both treatments; (2) fenofibrate and fasting regulate the mitochondrial levels of p43 and thus affect the efficiency of the direct T3 mitochondrial pathway.
【 授权许可】
Unknown
【 预 览 】
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