4.8 Article

Adipose Snail1 Regulates Lipolysis and Lipid Partitioning by Suppressing Adipose Triacylglycerol Lipase Expression

Journal

CELL REPORTS
Volume 17, Issue 8, Pages 2015-2027

Publisher

CELL PRESS
DOI: 10.1016/j.celrep.2016.10.070

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Funding

  1. National Institutes of Health (NIH) [DK091591, DK094014, AR065524]
  2. National Natural Science Foundation of China [31470798]
  3. Michigan Diabetes Research and Training Center [NIH DK20572]
  4. University of Michigan's Cancer Center [NIH CA46592]
  5. University of Michigan Nathan Shock Center [NIH P30AG013283]
  6. University of Michigan Gut Peptide Research Center [NIH DK34933]

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Lipolysis provides metabolic fuel; however, aberrant adipose lipolysis results in ectopic lipid accumulation and lipotoxicity. While adipose triacylglycerol lipase (ATGL) catalyzes the first step of lipolysis, its regulation is not fully understood. Here, we demonstrate that adipocyte Snail1 suppresses both ATGL expression and lipolysis. Adipose Snail1 levels are higher in fed mice than in fasted mice and higher in obese mice as opposed to lean mice. Insulin increases Snail1 levels in both murine and human adipocytes, wherein Snail1 binds to the ATGL promoter to repress its expression. Importantly, adipocyte-specific deletion of Snail1 increases adipose ATGL expression and lipolysis, resulting in decreased fat mass and increased liver fat content in mice fed either a normal chow diet or a high-fat diet. Thus, we have identified a Snail1-ATGL axis that regulates adipose lipolysis and fatty acid release, thereby governing lipid partitioning between adipose and nonadipose tissues.

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