Abstract
The hydrolysis of fat stored in adipose tissues is crucial for providing energy during fasting and exercise, and dysregulation of fat breakdown may contribute to metabolic disease. In this issue of Cell Metabolism, report that CGI-58/ABHD5, a lipid-droplet-associated protein that is mutated in a rare disease characterized by excess lipid storage, activates adipose triglyceride lipase and thus may regulate fat mobilization.
MeSH terms
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1-Acylglycerol-3-Phosphate O-Acyltransferase
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Adipose Tissue / enzymology*
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Animals
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Enzyme Activation
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Esterases / genetics
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Esterases / metabolism*
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Humans
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Lipase / genetics
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Lipase / metabolism*
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Lipid Metabolism, Inborn Errors / enzymology*
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Lipid Metabolism, Inborn Errors / genetics
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Lipolysis
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Mutation
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Phospholipases A / metabolism*
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Syndrome
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Triglycerides / metabolism*
Substances
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Triglycerides
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1-Acylglycerol-3-Phosphate O-Acyltransferase
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ABHD5 protein, human
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Esterases
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Lipase
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PNPLA2 protein, human
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Phospholipases A