Fas/Fas ligand up-regulation and Bcl-2 down-regulation may be significant in the pathogenesis of Hashimoto's thyroiditis

J Clin Endocrinol Metab. 1998 Jun;83(6):2199-203. doi: 10.1210/jcem.83.6.4853.

Abstract

Hashimoto's thyroiditis (HT) is an autoimmune disorder characterized by diffuse thyroid lymphocytic infiltration and follicle destruction. Cross-linking of the Fas receptor with its own ligand (FasL) triggers apoptosis in various systems, whereas the Bcl-2 protooncogene inhibits apoptotic cell death. The involvement of Fas, FasL, and Bcl-2 in the apoptotic process in HT was evaluated in 15 thyroid tissue samples from patients with HT stained for apoptosis and for Fas, FasL, and Bcl-2 protein expression. Eight samples from healthy thyroid tissue were used for comparison. Thyroid follicles in HT samples exhibited strong staining for Fas and FasL and a high percentage of apoptosis (30.3 +/- 14.5%, mean +/- SD), in contrast to normal control follicles that exhibited moderate Fas, minimal or no FasL, and hardly any apoptosis. Immunostaining for Bcl-2 was high in normal, and weak in involved, thyroid follicles. Infiltrating lymphocytes stained weakly for FasL and strongly for Bcl-2. We conclude that follicular cells in HT undergo apoptosis by concomitant up-regulation of FasL and Fas and down-regulation of Bcl-2 protein. The lymphocytes do not seem to be directly engaged in the process with their own FasL, but they may provide the appropriate cytokine milieu that, in turn, up-regulates Fas and/or FasL leading to apoptosis.

MeSH terms

  • Adolescent
  • Adult
  • Apoptosis
  • Cross-Linking Reagents
  • Fas Ligand Protein
  • Female
  • Humans
  • Male
  • Membrane Glycoproteins / metabolism*
  • Middle Aged
  • Proto-Oncogene Proteins c-bcl-2 / metabolism*
  • Thyroid Gland / metabolism
  • Thyroiditis, Autoimmune / etiology
  • Thyroiditis, Autoimmune / metabolism*
  • Thyroiditis, Autoimmune / pathology
  • fas Receptor / metabolism*

Substances

  • Cross-Linking Reagents
  • FASLG protein, human
  • Fas Ligand Protein
  • Membrane Glycoproteins
  • Proto-Oncogene Proteins c-bcl-2
  • fas Receptor