TSH controls Ref-1 nuclear translocation in thyroid cells

J Mol Endocrinol. 2000 Jun;24(3):383-90. doi: 10.1677/jme.0.0240383.

Abstract

Ref-1 (called also APE) is a bifunctional protein playing a role in a large variety of cell functions. It is a major member of the DNA base excision repair system. Moreover, through reduction of cysteine residues, Ref-1 controls the activity of several transcription factors. It has been previously demonstrated that TSH up-regulates Ref-1 gene expression in thyroid cells. By using the rat FRTL-5 cell line, we demonstrate that TSH controls Ref-1 intracellular localization. Western blot experiments indicate that addition of TSH to the culture medium increases the Ref-1 cytoplasm-to-nucleus translocation. This phenomenon occurs at early times of TSH stimulation and is not dependent on protein neosynthesis. The Ref-1 cellular compartmentalization was also investigated in human thyroid tumors. A Ref-1 nuclear/cytoplasmic ratio difference between normal and cancerous thyroid tissues was observed. These results suggest that Ref-1 localization may have a critical role in the control of thyroid cell functions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biological Transport
  • Carbon-Oxygen Lyases / metabolism*
  • Cell Line
  • Cell Nucleus / metabolism*
  • Cytoplasm / metabolism
  • DNA-(Apurinic or Apyrimidinic Site) Lyase*
  • Humans
  • Rats
  • Thyroid Gland / cytology
  • Thyroid Gland / metabolism*
  • Thyrotropin / physiology*

Substances

  • Thyrotropin
  • Carbon-Oxygen Lyases
  • APEX1 protein, human
  • Apex1 protein, rat
  • DNA-(Apurinic or Apyrimidinic Site) Lyase