Liver-specific insulin receptor isoform A expression enhances hepatic glucose uptake and ameliorates liver steatosis in a mouse model of diet-induced obesity

Dis Model Mech. 2019 Feb 7;12(2):dmm036186. doi: 10.1242/dmm.036186.

Abstract

Among the main complications associated with obesity are insulin resistance and altered glucose and lipid metabolism within the liver. It has previously been described that insulin receptor isoform A (IRA) favors glucose uptake and glycogen storage in hepatocytes compared with isoform B (IRB), improving glucose homeostasis in mice lacking liver insulin receptor. Thus, we hypothesized that IRA could also improve glucose and lipid metabolism in a mouse model of high-fat-diet-induced obesity. We addressed the role of insulin receptor isoforms in glucose and lipid metabolism in vivo We expressed IRA or IRB specifically in the liver by using adeno-associated viruses (AAVs) in a mouse model of diet-induced insulin resistance and obesity. IRA, but not IRB, expression induced increased glucose uptake in the liver and muscle, improving insulin tolerance. Regarding lipid metabolism, we found that AAV-mediated IRA expression also ameliorated hepatic steatosis by decreasing the expression of Fasn, Pgc1a, Acaca and Dgat2 and increasing Scd-1 expression. Taken together, our results further unravel the role of insulin receptor isoforms in hepatic glucose and lipid metabolism in an insulin-resistant scenario. Our data strongly suggest that IRA is more efficient than IRB at favoring hepatic glucose uptake, improving insulin tolerance and ameliorating hepatic steatosis. Therefore, we conclude that a gene therapy approach for hepatic IRA expression could be a safe and promising tool for the regulation of hepatic glucose consumption and lipid metabolism, two key processes in the development of non-alcoholic fatty liver disease associated with obesity.This article has an associated First Person interview with the first author of the paper.

Keywords: Adeno-associated viruses; Gene therapy; Glucose metabolism; Insulin receptor isoforms; Insulin resistance; Non-alcoholic fatty liver disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Dependovirus / metabolism
  • Diet, High-Fat
  • Disease Models, Animal
  • Fatty Liver / metabolism*
  • Fatty Liver / pathology*
  • Gene Expression Regulation
  • Glucose / metabolism*
  • Insulin Resistance
  • Insulin Secretion
  • Lipid Metabolism / genetics
  • Liver / metabolism*
  • Male
  • Mice, Inbred C57BL
  • Muscles / metabolism
  • Obesity / metabolism*
  • Organ Specificity
  • Protein Isoforms / metabolism
  • Receptor, Insulin / metabolism*

Substances

  • Protein Isoforms
  • Receptor, Insulin
  • Glucose