Kate Townsend Creasy, Minal B. Mehta, Carolin V. Schneider, Joseph Park, David Zhang, Swapnil V. Shewale, John S. Millar, Marijana Vujkovic, Nicholas J. Hand, Paul M. Titchenell, Joseph A. Baur, Daniel J. Rader
{"title":"Ppp1r3b is a metabolic switch that shifts hepatic energy storage from lipid to glycogen","authors":"Kate Townsend Creasy, Minal B. Mehta, Carolin V. Schneider, Joseph Park, David Zhang, Swapnil V. Shewale, John S. Millar, Marijana Vujkovic, Nicholas J. Hand, Paul M. Titchenell, Joseph A. Baur, Daniel J. Rader","doi":"10.1126/sciadv.ado3440","DOIUrl":null,"url":null,"abstract":"<div >The <i>PPP1R3B</i> gene, encoding PPP1R3B protein, is critical for liver glycogen synthesis and maintaining blood glucose levels. Genetic variants affecting <i>PPP1R3B</i> expression are associated with several metabolic traits and liver disease, but the precise mechanisms are not fully understood. We studied the effects of both <i>Ppp1r3b</i> overexpression and deletion in mice and cell models and found that both changes in <i>Ppp1r3b</i> expression result in dysregulated metabolism and liver damage, with overexpression increasing liver glycogen stores, while deletion resulted in higher liver lipid accumulation. These patterns were confirmed in humans where variants increasing <i>PPP1R3B</i> expression had lower liver fat and decreased plasma lipids, whereas putative loss-of-function variants were associated with increased liver fat and elevated plasma lipids. These findings support that PPP1R3B is a crucial regulator of hepatic metabolism beyond glycogen synthesis and that genetic variants affecting <i>PPP1R3B</i> expression levels influence if hepatic energy is stored as glycogen or triglycerides.</div>","PeriodicalId":21609,"journal":{"name":"Science Advances","volume":"11 20","pages":""},"PeriodicalIF":11.7000,"publicationDate":"2025-05-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.science.org/doi/reader/10.1126/sciadv.ado3440","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Science Advances","FirstCategoryId":"103","ListUrlMain":"https://www.science.org/doi/10.1126/sciadv.ado3440","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
The PPP1R3B gene, encoding PPP1R3B protein, is critical for liver glycogen synthesis and maintaining blood glucose levels. Genetic variants affecting PPP1R3B expression are associated with several metabolic traits and liver disease, but the precise mechanisms are not fully understood. We studied the effects of both Ppp1r3b overexpression and deletion in mice and cell models and found that both changes in Ppp1r3b expression result in dysregulated metabolism and liver damage, with overexpression increasing liver glycogen stores, while deletion resulted in higher liver lipid accumulation. These patterns were confirmed in humans where variants increasing PPP1R3B expression had lower liver fat and decreased plasma lipids, whereas putative loss-of-function variants were associated with increased liver fat and elevated plasma lipids. These findings support that PPP1R3B is a crucial regulator of hepatic metabolism beyond glycogen synthesis and that genetic variants affecting PPP1R3B expression levels influence if hepatic energy is stored as glycogen or triglycerides.
期刊介绍:
Science Advances, an open-access journal by AAAS, publishes impactful research in diverse scientific areas. It aims for fair, fast, and expert peer review, providing freely accessible research to readers. Led by distinguished scientists, the journal supports AAAS's mission by extending Science magazine's capacity to identify and promote significant advances. Evolving digital publishing technologies play a crucial role in advancing AAAS's global mission for science communication and benefitting humankind.