ErbB4 deletion predisposes to development of metabolic syndrome in mice

Am J Physiol Endocrinol Metab. 2018 Oct 1;315(4):E583-E593. doi: 10.1152/ajpendo.00166.2018. Epub 2018 Jun 26.

Abstract

ErbB4, a member of the EGF receptor family, plays a variety of roles in physiological and pathological states. Genetic studies have indicated a link between ErbB4 and type 2 diabetes and obesity, but its role in metabolic syndrome (MetS) has not been reported. In the current study we found that mice with ErbB4 deletion developed MetS after 24 wk on a medium-fat diet (MFD), as indicated by development of obesity, dyslipidemia, hepatic steatosis, hyperglycemia, hyperinsulinemia, and insulin resistance, compared with wild-type mice. ErbB4 deletion mice also exhibited increased amounts of subcutaneous and visceral fat, with increased serum leptin levels, compared with wild-type mice, whereas levels of adiponectin were not significantly different. Histologically, severe inflammation, indicated by F4/80 immunostaining and M1 macrophage polarization, was detected in inguinal and epididymal white adipose tissue in ErbB4 deletion mice. ErbB4 expression decreased during 3T3-L1 preadipocyte differentiation. Administration of neuroregulin 4, a specific ligand for ErbB4, to 3T3-L1 adipocytes had no effect on adipogenesis and lipolysis but significantly inhibited lipogenesis, promoted browning, induced GLUT4 redistribution to the cell membrane, and increased glucose uptake. Neuroregulin 4 also significantly increased glucose uptake in adipocytes isolated from wild-type mice, while these effects were significantly decreased in adipocytes isolated from ErbB4 deletion mice. In conclusion, our results indicate that ErbB4 may play an important role in glucose homeostasis and lipogenesis. ErbB4 deficiency-related obesity and adipose tissue inflammation may contribute to the development of MetS.

Keywords: ErbB4; inflammation; insulin resistance; lipogenesis; neuregulin 4.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • 3T3-L1 Cells
  • Adipogenesis / drug effects
  • Adiponectin / metabolism
  • Adipose Tissue, White / immunology
  • Animals
  • Dietary Fats*
  • Dyslipidemias / genetics*
  • Fatty Liver / genetics*
  • Gene Deletion
  • Genetic Predisposition to Disease
  • Glucose Transporter Type 4 / drug effects
  • Glucose Transporter Type 4 / metabolism
  • Hyperglycemia / genetics*
  • Hyperinsulinism / genetics
  • Inflammation
  • Insulin Resistance / genetics*
  • Intra-Abdominal Fat
  • Leptin / metabolism
  • Lipogenesis / drug effects
  • Macrophages
  • Male
  • Metabolic Syndrome / genetics*
  • Mice
  • Neuregulins / pharmacology
  • Obesity / genetics*
  • Receptor, ErbB-4 / genetics*
  • Subcutaneous Fat

Substances

  • Adiponectin
  • Dietary Fats
  • Glucose Transporter Type 4
  • Leptin
  • Neuregulins
  • Slc2a4 protein, mouse
  • neuregulin-4
  • Erbb4 protein, mouse
  • Receptor, ErbB-4