TGF-beta control of rat thyroid follicular cells differentiation

Mol Cell Endocrinol. 2003 Sep 30;207(1-2):1-11. doi: 10.1016/s0303-7207(03)00238-7.

Abstract

TGF-beta1 is a potent inhibitor of growth and DNA synthesis in thyroid cells. It has also been shown that TGF-beta1 inhibits thyrocyte function. The functional inhibition is represented by a downregulation of thyroid specific genes, such as Na(+)/I(-) symporter (NIS), thyroglobulin (TG) and thyroperoxidase (TPO). The transcriptional control of these genes is mediated by thyroid-specific transcription factors: thyroid transcription factor-1 (TTF-1) and PAX-8. It has been shown that Smad proteins play a pivotal role in the intracellular signal transduction of the TGF-beta family members. In this paper, the functional relevance of Smad4, in the control of thyroid differentiation genes and thyroid-specific transcription factors, has been investigated. The data obtained provides, for the first time, evidence that D.N. Smad4-100T is capable of blocking TGF-beta1 action in the regulation of thyroid-specific genes expression. Such action is possible by blocking nuclear translocation of Smad4 and Smad2.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autoantigens / genetics
  • Autoantigens / physiology
  • Blotting, Northern
  • Blotting, Western
  • Cell Differentiation / drug effects*
  • Cell Line
  • Clone Cells
  • Cysteine Endopeptidases / genetics
  • Cysteine Endopeptidases / metabolism
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • DNA-Binding Proteins / physiology
  • Down-Regulation
  • Gene Expression Regulation / drug effects
  • Genetic Vectors / genetics
  • Immunohistochemistry
  • Iodide Peroxidase / genetics
  • Iodide Peroxidase / physiology
  • Iron-Binding Proteins / genetics
  • Iron-Binding Proteins / physiology
  • Luciferases / genetics
  • Luciferases / metabolism
  • Mutation / genetics
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism
  • PAX8 Transcription Factor
  • Paired Box Transcription Factors
  • Phosphorylation
  • Rats
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • Signal Transduction / physiology
  • Smad2 Protein
  • Smad4 Protein
  • Symporters / genetics
  • Symporters / physiology
  • Thyroid Gland / cytology
  • Thyroid Gland / drug effects*
  • Thyroid Nuclear Factor 1
  • Thyrotropin / pharmacology
  • Trans-Activators / genetics
  • Trans-Activators / metabolism
  • Trans-Activators / physiology
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Transfection
  • Transforming Growth Factor beta / pharmacology*
  • Transforming Growth Factor beta / physiology
  • Transforming Growth Factor beta1

Substances

  • Autoantigens
  • DNA-Binding Proteins
  • Iron-Binding Proteins
  • NKX2-1 protein, human
  • Nkx2-1 protein, rat
  • Nuclear Proteins
  • PAX8 Transcription Factor
  • Paired Box Transcription Factors
  • Pax8 protein, rat
  • Recombinant Fusion Proteins
  • Smad2 Protein
  • Smad2 protein, rat
  • Smad4 Protein
  • Smad4 protein, rat
  • Symporters
  • TGFB1 protein, human
  • Tgfb1 protein, rat
  • Thyroid Nuclear Factor 1
  • Trans-Activators
  • Transcription Factors
  • Transforming Growth Factor beta
  • Transforming Growth Factor beta1
  • sodium-iodide symporter
  • Thyrotropin
  • TPO protein, human
  • Iodide Peroxidase
  • Luciferases
  • Cysteine Endopeptidases
  • cysteine proteinase I