A small molecule differentiation inducer increases insulin production by pancreatic β cells

Proc Natl Acad Sci U S A. 2011 Dec 20;108(51):20713-8. doi: 10.1073/pnas.1118526109. Epub 2011 Dec 5.

Abstract

New drugs for preserving and restoring pancreatic β-cell function are critically needed for the worldwide epidemic of type 2 diabetes and the cure for type 1 diabetes. We previously identified a family of neurogenic 3,5-disubstituted isoxazoles (Isx) that increased expression of neurogenic differentiation 1 (NeuroD1, also known as BETA2); this transcription factor functions in neuronal and pancreatic β-cell differentiation and is essential for insulin gene transcription. Here, we probed effects of Isx on human cadaveric islets and MIN6 pancreatic β cells. Isx increased the expression and secretion of insulin in islets that made little insulin after prolonged ex vivo culture and increased expression of neurogenic differentiation 1 and other regulators of islet differentiation and insulin gene transcription. Within the first few hours of exposure, Isx caused biphasic activation of ERK1/2 and increased bulk histone acetylation. Although there was little effect on histone deacetylase activity, Isx increased histone acetyl transferase activity in nuclear extracts. Reconstitution assays indicated that Isx increased the activity of the histone acetyl transferase p300 through an ERK1/2-dependent mechanism. In summary, we have identified a small molecule with antidiabetic activity, providing a tool for exploring islet function and a possible lead for therapeutic intervention in diabetes.

Publication types

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

MeSH terms

  • Animals
  • Basic Helix-Loop-Helix Transcription Factors / metabolism
  • Cell Differentiation
  • Cell Nucleus / metabolism
  • Gene Expression Regulation
  • Glucose / metabolism
  • HEK293 Cells
  • Humans
  • Insulin / metabolism*
  • Insulin-Secreting Cells / cytology*
  • Islets of Langerhans / metabolism
  • Isoxazoles / pharmacology*
  • Mice
  • Neurons / metabolism
  • Transcription Factors / metabolism
  • p300-CBP Transcription Factors / metabolism

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • Insulin
  • Isoxazoles
  • NEUROD1 protein, human
  • Neurod1 protein, mouse
  • Transcription Factors
  • p300-CBP Transcription Factors
  • Glucose