4.5 Article

Isoform-specific increases in murine skeletal muscle peroxisome proliferator-activated receptor-γ coactivator-1α (PGC-1α) mRNA in response to β2-adrenergic receptor activation and exercise

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ENDOCRINOLOGY
卷 149, 期 9, 页码 4527-4533

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ENDOCRINE SOC
DOI: 10.1210/en.2008-0466

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Adrenergic receptor (AR) activation increases expression of peroxisome proliferator-activated receptor (PPAR)-gamma coactivator 1 alpha(PGC-1 alpha) mRNA, which may promote mitochondrial biogenesis in skeletal muscles. An AR-activated increase in PGC-1 alpha mRNA was observed in exercise. PGC-1 alpha mRNA is considered a single transcript (PGC-1 alpha-a); however, a transcript search of PGC-1 alpha in expressed sequence tag libraries revealed that two novel isoforms of PGC-1 alpha mRNA, named PGC-1 alpha-b and PGC-1 alpha-c, were expressed in mice tissues. Compared with PGC-1 alpha-a mRNA (a previously described isoform), PGC-1 alpha-b or PGC-1 alpha-c mRNA was transcribed by a different exon 1 of the PGC-1 alpha gene and produced slightly smaller-sized proteins. PGC-1 alpha-b or PGC-1 alpha-c protein was functional; both isoforms possessed transcriptional activity and could coactivate PPARs, similar to those in PGC-1 alpha-a in vitro. Transgenic mice overexpressing PGC-1 alpha-b or PGC-1 alpha-c in skeletal muscles showed increased gene expression related to mitochondrial biogenesis and fatty acid oxidation. In C57BL/6J mice, injection of the beta 2-AR agonist clenbuterol increased PGC-1 alpha-b and PGC-1 alpha- c mRNA expression more than 350-fold, but not PGC-1 alpha-a, in skeletal muscle. A single bout of exercise also increased PGC-1 alpha-b and PGC-1 alpha-c mRNAs, but not PGC-1 alpha-a, in skeletal muscles. The increases in skeletal muscles in response to exercise were inhibited by pretreatment with the beta 2-AR-specific inhibitor ICI 118,551. However, in liver, fasting increased PGC-1 alpha-a mRNA, but not PGC-1 alpha-b and PGC-1 alpha-c mRNAs. These data indicate that AR activation is a major mechanism of an increase in PGC-1 alpha expression in skeletal muscles, and the increase in PGC-1 alpha mRNAs was isoform specific.

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