Retinoid X receptor α acts as a negative regulator in Nurr1-induced dopaminergic differentiation in rat neural precursor cells

Neuroreport. 2010 Dec 29;21(18):1162-6.

Abstract

To investigate the role of retinoid X receptor (RXRα)–Nurr1 heterodimers in tyrosine hydroxylase (TH) expression, we observed retrovirus-induced RXRα–Nurr1 heterodimer interactions with, and transactivation of, the TH promoter region in cultured rat embryonic neural precursor cells. Interestingly, forced expression of RXRα with Nurr1 remarkably reduced Nurr1 activity in TH+ dopaminergic neuron generation and significantly down-regulated TH promoter activity. These regulatory activities were altered in both Nurr1dim- and RXRαdim- that disrupted dimeric binding, verifying that the Nurr1–RXRα heterodimer represses TH promoter activity. Therefore, a plausible explanation for the inhibitory role of RXRα in Nurr1-induced TH expression is that RXRα differentially affects an inhibitory element of the TH promoter.

MeSH terms

  • Animals
  • Cell Differentiation / genetics
  • Cell Differentiation / physiology*
  • Cells, Cultured
  • Dopamine / physiology*
  • Down-Regulation / genetics
  • Down-Regulation / physiology*
  • Embryonic Stem Cells / cytology*
  • Embryonic Stem Cells / enzymology
  • Embryonic Stem Cells / metabolism
  • Humans
  • Neural Inhibition / genetics
  • Neurons / cytology*
  • Neurons / enzymology
  • Neurons / metabolism
  • Nuclear Receptor Subfamily 4, Group A, Member 2 / antagonists & inhibitors*
  • Nuclear Receptor Subfamily 4, Group A, Member 2 / metabolism
  • Nuclear Receptor Subfamily 4, Group A, Member 2 / physiology
  • Promoter Regions, Genetic
  • Protein Interaction Mapping
  • Protein Multimerization / genetics
  • Rats
  • Retinoid X Receptor alpha / metabolism
  • Retinoid X Receptor alpha / physiology*
  • Trans-Activators / antagonists & inhibitors
  • Trans-Activators / genetics
  • Trans-Activators / metabolism
  • Tyrosine 3-Monooxygenase / antagonists & inhibitors
  • Tyrosine 3-Monooxygenase / genetics
  • Tyrosine 3-Monooxygenase / metabolism

Substances

  • NR4A2 protein, human
  • Nuclear Receptor Subfamily 4, Group A, Member 2
  • Retinoid X Receptor alpha
  • Trans-Activators
  • Tyrosine 3-Monooxygenase
  • Dopamine