Journal
CELL METABOLISM
Volume 16, Issue 1, Pages 104-112Publisher
CELL PRESS
DOI: 10.1016/j.cmet.2012.05.010
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Funding
- NIH [P01 DK56116, R37 DK43051, GM56203, CA120964, K99/R00-CA133245]
- BADERC [DK57521]
- Picower Foundation
- JPB Foundation
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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 (alpha 2AMPK as the site of convergence and show that p70S6 kinase forms a complex with alpha 2AMPK, resulting in phosphorylation on serine491. Blocking alpha 2AMPK-serine(491) phosphorylation increases hypothalamic food intake, and body weight. is necessary for leptin's effects on hypothalamic alpha 2AMPK 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.
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