SIRT1 controls lipolysis in adipocytes via FOXO1-mediated expression of ATGL

• DOI: 10.1194/jlr.m014647
• Publication Date: 2011-07-09T04:38:52Z
• Authors: Partha Chakrabarti; Taylor English; Shakun Karki; Li Qiang; Rong Tao; Juyoun Kim; Zhijun Luo; Stephen R. Farmer; Konstantin V. Kan...
• Keywords: 0301 basic medicine; adipose triglyceride lipase; Lipolysis; Down-Regulation; fatty acid/metabolism; QD415-436; Biochemistry; Gene Expression Regulation, Enzymologic; Mice; 03 medical and health sciences; Sirtuin 1; 3T3-L1 Cells; Adipocytes; Animals; RNA, Small Interfering; dyslipidemias; Promoter Regions, Genetic; Forkhead Box Protein O1; Adenylate Kinase; Forkhead Transcription Factors; Lipase; Lipid Metabolism; adipose tissue; PPAR gamma; Gene Knockdown Techniques

Recent studies have established SIRT1 as an important regulator of lipid metabolism, although the mechanism of its action at the molecular level has not been revealed. Here, we show that knockdown of SIRT1 with the help of small hairpin RNA decreases basal and isoproterenol-stimulated lipolysis in cultured adipocytes. This effect is attributed, at least in part, to the suppression of the rate-limiting lipolytic enzyme, adipose triglyceride lipase (ATGL), at the level of transcription. Mechanistically, SIRT1 controls acetylation status and functional activity of FoxO1 that directly binds to the ATGL promoter and regulates ATGL gene transcription. We have also found that depletion of SIRT1 decreases AMP-dependent protein kinase (AMPK) activity in adipocytes. To determine the input of AMPK in regulation of lipolysis, we have established a stable adipose cell line that expresses a dominant-negative α1 catalytic subunit of AMPK under the control of the inducible TET-OFF lentiviral expression vector. Reduction of AMPK activity does not have a significant effect on the rates of lipolysis in this cell model. We conclude, therefore, that SIRT1 controls ATGL transcription primarily by deacetylating FoxO1.