G protein-coupled receptor 151 regulates glucose metabolism and hepatic gluconeogenesis

Author:

Bielczyk-Maczynska EwaORCID,Zhao MengORCID,Zushin Peter-James H.ORCID,Schnurr Theresia M.,Kim Hyun-JungORCID,Li Jiehan,Nallagatla Pratima,Sangwung PanjamapornORCID,Park Chong Y.,Cornn Cameron,Stahl AndreasORCID,Svensson Katrin J.ORCID,Knowles Joshua W.ORCID

Abstract

AbstractHuman genetics has been instrumental in identification of genetic variants linked to type 2 diabetes. Recently a rare, putative loss-of-function mutation in the orphan G-protein coupled receptor 151 (GPR151) was found to be associated with lower odds ratio for type 2 diabetes, but the mechanism behind this association has remained elusive. Here we show that Gpr151 is a fasting- and glucagon-responsive hepatic gene which regulates hepatic gluconeogenesis. Gpr151 ablation in mice leads to suppression of hepatic gluconeogenesis genes and reduced hepatic glucose production in response to pyruvate. Importantly, the restoration of hepatic Gpr151 levels in the Gpr151 knockout mice reverses the reduced hepatic glucose production. In this work, we establish a previously unknown role of Gpr151 in the liver that provides an explanation to the lowered type 2 diabetes risk in individuals with nonsynonymous mutations in GPR151.

Funder

American Heart Association

Novo Nordisk Fonden

U.S. Department of Health & Human Services | NIH | National Institute of Diabetes and Digestive and Kidney Diseases

Merck, the Jacob Churg Foundation, the McCormick and Gabilan Award, and the Stanford Cardiovascular Institute

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry,Multidisciplinary

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