PPP1R3C mediates metformin-inhibited hepatic gluconeogenesis

Metabolism. 2019 Sep:98:62-75. doi: 10.1016/j.metabol.2019.06.002. Epub 2019 Jun 8.

Abstract

Background: Metformin has been widely used to alleviate hyperglycemia in patients with type 2 diabetes mainly via suppressing hepatic gluconeogenesis. However, the underlying mechanism remains incompletely clear. Here, we aimed to explore the role of PPP1R3C in metformin-mediated inhibition of hepatic gluconeogenesis.

Methods: The differentially expressed genes in primary mouse hepatocytes incubated with 8-Br-cAMP and metformin were analyzed by microarrays. Hepatic glucose production and gluconeogenic gene expressions were detected after adenovirus-mediated overexpression or silence of PPP1R3C in vitro and in vivo. The phosphorylation level and location of transducer of regulated CREB activity 2 (TORC2) were determined by Western blot and immunofluorescence.

Results: Metformin and adenovirus-mediated activation of AMPK suppressed 8-Br-cAMP-stimulated Ppp1r3c mRNA expression in primary mouse hepatocytes. Overexpression of PPP1R3C in primary mouse hepatocytes or the livers of wild-type mice promoted hepatic glucose production and gluconeogenic gene expressions. On the contrary, adenovirus-mediated knockdown of PPP1R3C in primary mouse hepatocytes decreased hepatic gluconeogenesis, with the suppression of cAMP-stimulated gluconeogenic gene expressions and TORC2 dephosphorylation. Notably, Ppp1r3c expression was increased in the liver of db/db mice. After PPP1R3C silence in the livers of wild-type and db/db mice, blood glucose levels and hepatic glucose production were markedly lowered, with decreased expressions of key gluconeogenic enzymes and transcript factors as well as liver glycogen content.

Conclusion: Metformin-activated AMPK decreases hepatic PPP1R3C expression, leading to the suppression of hepatic gluconeogenesis through blocking cAMP-stimulated TORC2 dephosphorylation. Hepatic specific silence of PPP1R3C provides a promising therapeutic strategy for type 2 diabetes.

Keywords: AMPK; Gluconeogenesis; Liver; Metformin; PPP1R3C; TORC2.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 8-Bromo Cyclic Adenosine Monophosphate
  • Animals
  • Blood Glucose / metabolism
  • Gene Expression / drug effects
  • Gene Knockdown Techniques
  • Gluconeogenesis / drug effects*
  • Gluconeogenesis / genetics
  • Hepatocytes / drug effects
  • Hypoglycemic Agents / pharmacology*
  • Intracellular Signaling Peptides and Proteins / genetics
  • Intracellular Signaling Peptides and Proteins / metabolism*
  • Liver / drug effects
  • Liver / metabolism*
  • Liver Glycogen / metabolism
  • Male
  • Mechanistic Target of Rapamycin Complex 1 / metabolism
  • Metformin / pharmacology*
  • Mice
  • Mice, Inbred C57BL
  • Primary Cell Culture

Substances

  • Blood Glucose
  • Hypoglycemic Agents
  • Intracellular Signaling Peptides and Proteins
  • Liver Glycogen
  • Ppp1r3c protein, mouse
  • 8-Bromo Cyclic Adenosine Monophosphate
  • Metformin
  • Mechanistic Target of Rapamycin Complex 1