| Literature DB >> 18585098 |
Takeshi Inagaki1, Vicky Y Lin, Regina Goetz, Moosa Mohammadi, David J Mangelsdorf, Steven A Kliewer.
Abstract
Starvation blocks the actions of growth hormone (GH) and inhibits growth through mechanisms that are not well understood. In this report, we demonstrate that fibroblast growth factor 21 (FGF21), a hormone induced by fasting, causes GH resistance. In liver, FGF21 reduces concentrations of the active form of signal transducer and activator of transcription 5 (STAT5), a major mediator of GH actions, and causes corresponding decreases in the expression of its target genes, including insulin-like growth factor 1 (IGF-1). FGF21 also induces hepatic expression of IGF-1 binding protein 1 and suppressor of cytokine signaling 2, which blunt GH signaling. Chronic exposure to FGF21 markedly inhibits growth in mice. These data suggest a central role for FGF21 in inhibiting growth as part of its broader role in inducing the adaptive response to starvation.Entities:
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Year: 2008 PMID: 18585098 PMCID: PMC2575072 DOI: 10.1016/j.cmet.2008.05.006
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287