Thyroid hormone promotes postnatal rat pancreatic β-cell development and glucose-responsive insulin secretion through MAFA

Diabetes. 2013 May;62(5):1569-80. doi: 10.2337/db12-0849. Epub 2013 Jan 10.

Abstract

Neonatal β cells do not secrete glucose-responsive insulin and are considered immature. We previously showed the transcription factor MAFA is key for the functional maturation of β cells, but the physiological regulators of this process are unknown. Here we show that postnatal rat β cells express thyroid hormone (TH) receptor isoforms and deiodinases in an age-dependent pattern as glucose responsiveness develops. In vivo neonatal triiodothyronine supplementation and TH inhibition, respectively, accelerated and delayed metabolic development. In vitro exposure of immature islets to triiodothyronine enhanced the expression of Mafa, the secretion of glucose-responsive insulin, and the proportion of responsive cells, all of which are effects that were abolished in the presence of dominant-negative Mafa. Using chromatin immunoprecipitation and electrophoretic mobility shift assay, we show that TH has a direct receptor-ligand interaction with the Mafa promoter and, using a luciferase reporter, that this interaction was functional. Thus, TH can be considered a physiological regulator of functional maturation of β cells via its induction of Mafa.

Publication types

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

MeSH terms

  • Animals
  • Animals, Newborn
  • Blood Glucose / analysis*
  • Cell Differentiation*
  • Cell Nucleus / metabolism
  • Gene Expression Regulation, Developmental
  • Genes, Reporter
  • Insulin / metabolism*
  • Insulin Secretion
  • Insulin-Secreting Cells / cytology*
  • Insulin-Secreting Cells / metabolism
  • Iodide Peroxidase / genetics
  • Iodide Peroxidase / metabolism
  • Islets of Langerhans / cytology
  • Islets of Langerhans / growth & development
  • Islets of Langerhans / metabolism
  • Promoter Regions, Genetic
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism
  • Protein Transport
  • Proto-Oncogene Proteins c-maf / genetics
  • Proto-Oncogene Proteins c-maf / metabolism*
  • Random Allocation
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Thyroid Hormone / genetics
  • Receptors, Thyroid Hormone / metabolism
  • Recombinant Proteins / metabolism
  • Tissue Culture Techniques
  • Triiodothyronine / metabolism*

Substances

  • Blood Glucose
  • Insulin
  • Maf protein, rat
  • Protein Isoforms
  • Proto-Oncogene Proteins c-maf
  • Receptors, Thyroid Hormone
  • Recombinant Proteins
  • Triiodothyronine
  • Iodide Peroxidase