Orphan receptor COUP-TF I antagonizes retinoic acid-induced neuronal differentiation

J Neurosci Res. 1995 May 1;41(1):39-48. doi: 10.1002/jnr.490410106.

Abstract

Chicken ovalbumin upstream promoter-transcription factors (COUP-TF) are expressed in the developing nervous system and interact with nuclear hormone receptors to regulate expression of different genes. The role of COUP-TF orphan receptors in neurogenesis is virtually unknown. To study the possible function of COUP-TF I during neuronal differentiation, we generated COUP-TF I overexpressing teratocarcinoma PCC7 cell lines and analyzed retinoic acid (RA)-induced neuronal differentiation of these cells. COUP-TF I overexpression results in the blockade of morphological differentiation after induction to differentiate. COUP-TF I represses expression of microtubule-associated protein 2 (MAP2) gene and delays induction of growth-associated protein 43 (GAP43) gene expression. In contrast, expression of the neurofilament light subunit (NF-L) gene is not affected by COUP-TF I overexpression during neuronal differentiation. Also, cells overexpressing COUP-TF I do not stop proliferating after RA and dBcAMP treatment and possess suppressed transcriptional activation from different RA response elements. These results suggest that COUP-TF I plays an important role in regulating RA-induced neuronal differentiation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Biomarkers
  • Bucladesine / pharmacology
  • COUP Transcription Factor I
  • Cell Cycle / drug effects
  • Cell Cycle / genetics
  • Cell Differentiation / drug effects
  • Cell Differentiation / physiology
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / pharmacology*
  • Enhancer Elements, Genetic / genetics
  • GAP-43 Protein
  • Gene Expression / physiology
  • Membrane Glycoproteins / genetics
  • Mice
  • Microtubule-Associated Proteins / genetics
  • Molecular Sequence Data
  • Nerve Tissue Proteins / genetics
  • Neurofilament Proteins / genetics
  • Receptors, Glucocorticoid / physiology*
  • Teratocarcinoma / pathology
  • Teratocarcinoma / physiopathology
  • Transcription Factors / genetics
  • Transcription Factors / pharmacology*
  • Tretinoin / pharmacology*
  • Tumor Cells, Cultured / cytology

Substances

  • Biomarkers
  • COUP Transcription Factor I
  • DNA-Binding Proteins
  • GAP-43 Protein
  • Membrane Glycoproteins
  • Microtubule-Associated Proteins
  • Nerve Tissue Proteins
  • Neurofilament Proteins
  • Nr2f1 protein, mouse
  • Receptors, Glucocorticoid
  • Transcription Factors
  • Tretinoin
  • Bucladesine