Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8727377 | Gastroenterology | 2017 | 23 Pages |
Abstract
In mouse models of obesity, we found that PHLPP2 degradation induced lipogenesis without affecting gluconeogenesis. KCTD17, which is up-regulated in liver tissues of obese mice and patients with NAFLD, binds to phosphorylated PHLPP2 to target it for ubiquitin-mediated degradation; this increases expression of genes that regulate lipogenesis to promote hepatic steatosis. Inhibitors of this pathway might be developed for treatment of patients with NAFLD.
Keywords
LC/MS-MSPHLPP2SREBP1cDNLT2DmTORNAFLDHFDde novo lipogenesisnonalcoholic steatohepatitisNonalcoholic fatty liver diseasetriglycerideGene regulationType 2 diabeteshigh-fat dietInsulin signalingknockoutNash Signal transductionmammalian target of rapamycinpolymerase chain reactionPCRsterol regulatory element-binding protein 1cliquid chromatography–tandem mass spectrometry
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Authors
KyeongJin Kim, Dongryeol Ryu, Paola Dongiovanni, Lale Ozcan, Shruti Nayak, Beatrix Ueberheide, Luca Valenti, Johan Auwerx, Utpal B. Pajvani,