| First Author | Dagon Y | Year | 2012 |
| Journal | Cell Metab | Volume | 16 |
| Issue | 1 | Pages | 104-12 |
| PubMed ID | 22727014 | Mgi Jnum | J:187414 |
| Mgi Id | MGI:5436373 | Doi | 10.1016/j.cmet.2012.05.010 |
| Citation | Dagon Y, et al. (2012) p70S6 kinase phosphorylates AMPK on serine 491 to mediate leptin's effect on food intake. Cell Metab 16(1):104-12 |
| abstractText | The PI3K-AKT, mTOR-p70S6 kinase and AMPK pathways play distinct and critical roles in metabolic regulation. Each pathway is necessary for leptin's anorexigenic effects in the hypothalamus. Here we show that these pathways converge in an integrated phosphorylation cascade to mediate leptin action in the hypothalamus. We identify serine(491) on alpha2AMPK as the site of convergence and show that p70S6 kinase forms a complex with alpha2AMPK, resulting in phosphorylation on serine(491). Blocking alpha2AMPK-serine(491) phosphorylation increases hypothalamic AMPK activity, food intake, and body weight. Serine(491) phosphorylation is necessary for leptin's effects on hypothalamic alpha2AMPK activity, neuropeptide expression, food intake, and body weight. These results identify an inhibitory AMPK kinase, p70S6 kinase, and demonstrate that AMPK is a substrate for mTOR-p70S6 kinase. This discovery has broad biologic implications since mTOR-p70S6 kinase and AMPK have multiple, fundamental and generally opposing cellular effects that regulate metabolism, cell growth, and development. |
