Induction of insulin receptor substrate-2 expression by Fc fusion to exendin-4 overexpressed in E. coli: a potential long-acting glucagon-like peptide-1 mimetic

BMB Rep. 2010 Feb;43(2):146-9. doi: 10.5483/bmbrep.2010.43.2.146.

Abstract

Exendin-4 (Ex-4), a peptide secreted from the salivary glands of the Gila monster lizard, can increase pancreatic beta-cell growth and insulin secretion by activating glucagon-like peptide-1 receptor. In this study, we expressed a fusion protein consisting of exendin-4 and the human immunoglobulin heavy chain (Ex-4/IgG-Fc) in E. coli and explored its potential therapeutic use for the treatment of insulin-resistant type 2 diabetes. Here, we show that the Ex-4/IgG-Fc fusion protein induces expression of insulin receptor substrate-2 in rat insulinoma INS-1 cells. Our findings therefore suggest that Ex-4/IgG-Fc overexpressed in E. coli could be used as a potential, long-acting glucagon-like peptide-1 mimetic.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Diabetes Mellitus, Type 2 / drug therapy
  • Escherichia coli / metabolism
  • Exenatide
  • Glucagon-Like Peptide 1 / metabolism
  • Glucagon-Like Peptide-1 Receptor
  • Humans
  • Hypoglycemic Agents / metabolism
  • Hypoglycemic Agents / pharmacology*
  • Immunoglobulin Fc Fragments / genetics
  • Immunoglobulin Heavy Chains / genetics
  • Insulin Receptor Substrate Proteins / metabolism*
  • Insulin Resistance
  • Peptides / genetics
  • Peptides / metabolism
  • Peptides / pharmacology*
  • Rats
  • Receptors, Glucagon / metabolism
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • Recombinant Fusion Proteins / pharmacology
  • Venoms / genetics
  • Venoms / metabolism
  • Venoms / pharmacology*

Substances

  • GLP1R protein, human
  • Glp1r protein, rat
  • Glucagon-Like Peptide-1 Receptor
  • Hypoglycemic Agents
  • Immunoglobulin Fc Fragments
  • Immunoglobulin Heavy Chains
  • Insulin Receptor Substrate Proteins
  • Peptides
  • Receptors, Glucagon
  • Recombinant Fusion Proteins
  • Venoms
  • Glucagon-Like Peptide 1
  • Exenatide