| Literature DB >> 28877455 |
Judith Simcox1, Gisela Geoghegan1, John Alan Maschek1, Claire L Bensard2, Marzia Pasquali3, Ren Miao1, Sanghoon Lee1, Lei Jiang4, Ian Huck5, Erin E Kershaw6, Anthony J Donato7, Udayan Apte5, Nicola Longo3, Jared Rutter2, Renate Schreiber8, Rudolf Zechner8, James Cox1, Claudio J Villanueva9.
Abstract
Cold-induced thermogenesis is an energy-demanding process that protects endotherms against a reduction in ambient temperature. Using non-targeted liquid chromatography-mass spectrometry-based lipidomics, we identified elevated levels of plasma acylcarnitines in response to the cold. We found that the liver undergoes a metabolic switch to provide fuel for brown fat thermogenesis by producing acylcarnitines. Cold stimulates white adipocytes to release free fatty acids that activate the nuclear receptor HNF4α, which is required for acylcarnitine production in the liver and adaptive thermogenesis. Once in circulation, acylcarnitines are transported to brown adipose tissue, while uptake into white adipose tissue and liver is blocked. Finally, a bolus of L-carnitine or palmitoylcarnitine rescues the cold sensitivity seen with aging. Our data highlight an elegant mechanism whereby white adipose tissue provides long-chain fatty acids for hepatic carnitilation to generate plasma acylcarnitines as a fuel source for peripheral tissues in mice.Entities:
Keywords: CPT1; HNF4alpha; UCP1; acylcarnitines; adipocytes; aging; brown fat; liver; metabolism; thermogenesis
Mesh:
Substances:
Year: 2017 PMID: 28877455 PMCID: PMC5658052 DOI: 10.1016/j.cmet.2017.08.006
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287