Distinct expression of cyclooxygenase-1 and -2 in the human thymus

Eur J Immunol. 2002 May;32(5):1482-92. doi: 10.1002/1521-4141(200205)32:5<1482::AID-IMMU1482>3.0.CO;2-O.

Abstract

Cyclooxygenase (COX)-1 and -2 catalyze the formation of prostaglandins (PG). Given the role of COX and PG during intrathymic T cell development in the mouse, we investigated the expression and localization of these isozymes in the human thymus. mRNA and proteins correspondent to COX-1 and -2 were observed from whole thymus extracts. By immunohistochemistry, COX-2 was selectively localized in the medulla and it was predominant in a subset of stromal cells. By contrast, COX-1 was diffusely and exclusively present in the cortex, both in thymocytes at early stages of differentiation and in cytokeratin-positive epithelial cells, as demonstrated by double immunostaining and flow cytometry analysis. COX-2-positive cells in the medulla expressed cytokeratin and HLA-DR molecules, but they were negative for dendritic or macrophagic antigens. In addition, COX-2-positive cells expressed both the epidermal growth factor receptor and its ligand, the transforming growth factor-alpha. The inducible isoform of the PGE(2) synthase was also present in the same cells, while was absent from COX-1-expressing cells of the cortex. Finally, electron microscopy confirmed that COX-2 was mainly localized in the cytoplasm of cytokeratin-positive cells, along the rough endoplasmic reticulum. In conclusion, COX-2 and the inducible isoform of PGE(2) synthase appear to be constitutively and selectively present in medullary epithelial cells of the human thymus, whereas COX-1 is predominantly present in the thymic cortex, both in the stroma and in developing thymocytes.

MeSH terms

  • Child
  • Cyclooxygenase 1
  • Cyclooxygenase 2
  • ErbB Receptors / metabolism
  • Gene Expression
  • HLA-DR Antigens / metabolism
  • Humans
  • Immunohistochemistry
  • In Situ Hybridization
  • Intramolecular Oxidoreductases / metabolism
  • Isoenzymes / genetics
  • Isoenzymes / metabolism*
  • Keratins / metabolism
  • Membrane Proteins
  • Microscopy, Immunoelectron
  • Phenotype
  • Prostaglandin-E Synthases
  • Prostaglandin-Endoperoxide Synthases / genetics
  • Prostaglandin-Endoperoxide Synthases / metabolism*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Thymus Gland / anatomy & histology
  • Thymus Gland / enzymology*
  • Thymus Gland / immunology
  • Tissue Distribution
  • Transforming Growth Factor alpha / metabolism

Substances

  • HLA-DR Antigens
  • Isoenzymes
  • Membrane Proteins
  • RNA, Messenger
  • Transforming Growth Factor alpha
  • Keratins
  • Cyclooxygenase 1
  • Cyclooxygenase 2
  • PTGS1 protein, human
  • PTGS2 protein, human
  • Prostaglandin-Endoperoxide Synthases
  • ErbB Receptors
  • Intramolecular Oxidoreductases
  • Prostaglandin-E Synthases