Hondares Elayne, Pineda-Torra Inés, Iglesias Roser, Staels Bart, Villarroya Francesc, Giralt Marta
Department of Biochemistry and Molecular Biology, University of Barcelona, 08028 Barcelona, Spain.
Biochem Biophys Res Commun. 2007 Mar 23;354(4):1021-7. doi: 10.1016/j.bbrc.2007.01.092. Epub 2007 Jan 25.
PGC-1alpha induces mitochondrial biogenesis in muscle and its activity has been related to insulin sensitization. Here, we report that fibrates induce PGC-1alpha gene expression in muscle both in vivo and in vitro. However, only activation via PPARdelta but not PPARalpha underlies this effect. PPARdelta induces PGC-1alpha gene transcription through a PPAR-response element in the PGC-1alpha promoter. Moreover, PGC-1alpha coactivates the PPARdelta-responsiveness of its own gene. A further positive autoregulatory loop of control relies on the induction of PPARdelta expression by PGC-1alpha. These data point to a distinct value of PPARdelta rather than PPARalpha agonists in the improvement of oxidative metabolism in muscle.
PGC-1α可诱导肌肉中的线粒体生物合成,其活性与胰岛素敏感性有关。在此,我们报告贝特类药物在体内和体外均可诱导肌肉中PGC-1α基因表达。然而,这种效应仅通过PPARδ激活介导,而非PPARα。PPARδ通过PGC-1α启动子中的PPAR反应元件诱导PGC-1α基因转录。此外,PGC-1α共同激活其自身基因的PPARδ反应性。另一个正向自动调节控制环依赖于PGC-1α对PPARδ表达的诱导。这些数据表明,在改善肌肉氧化代谢方面,PPARδ激动剂而非PPARα激动剂具有独特价值。