The C-terminal domain of the adenomatous polyposis coli (Apc) protein is involved in thyroid morphogenesis and function

Med Mol Morphol. 2011 Dec;44(4):207-12. doi: 10.1007/s00795-010-0529-9. Epub 2011 Dec 17.

Abstract

Adenomatous polyposis coli (APC) is a multifunctional protein as well as a tumor suppressor. To determine the functions of the C-terminal domain of Apc, we have investigated Apc ( 1638T/1638T ) mice, which express a truncated Apc that lacks the C-terminal domain. Apc ( 1638T/1638T ) mice are tumor free and exhibit growth retardation. In the present study, we analyzed the morphology and functions of the thyroid gland in Apc ( 1638T/1638T ) mice. There was no significant difference in the basal concentration of serum thyroid hormones between Apc ( 1638T/1638T ) and Apc (+/+) mice. Thyroid follicle size was significantly larger in Apc ( 1638T/1638T ) mice than in Apc (+/+) mice. The extent of serum T4 elevation following exogenous thyroid-stimulating hormone (TSH) injection was lower in Apc ( 1638T/1638T ) mice than in Apc (+/+) mice. TSH also induced a greater reduction in thyroid follicle size in Apc ( 1638T/1638T ) mice than in Apc (+/+) mice. Analyses using immunohistochemistry and electron microscopy indicated that follicular epithelial cells in Apc ( 1638T/1638T ) mice had an enlarged rough endoplasmic reticulum of irregular shape. These results suggest that the C-terminal domain of Apc is involved in thyroid morphology and function.

MeSH terms

  • Adenomatous Polyposis Coli Protein / chemistry*
  • Adenomatous Polyposis Coli Protein / genetics
  • Adenomatous Polyposis Coli Protein / metabolism
  • Animals
  • Gene Expression Profiling
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Morphogenesis*
  • Peptide Fragments / chemistry*
  • Peptide Fragments / genetics
  • Peptide Fragments / metabolism
  • Protein Structure, Tertiary
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Sequence Deletion
  • Thyroid Gland / growth & development*
  • Thyroid Gland / metabolism
  • Thyroid Gland / ultrastructure
  • Thyrotropin / pharmacology
  • Thyrotropin / physiology
  • Thyroxine / blood
  • Triiodothyronine / blood

Substances

  • Adenomatous Polyposis Coli Protein
  • Peptide Fragments
  • Recombinant Proteins
  • Triiodothyronine
  • Thyrotropin
  • Thyroxine