Paracrine glucocorticoid activity produced by mouse thymic epithelial cells

FASEB J. 1999 May;13(8):893-901. doi: 10.1096/fasebj.13.8.893.

Abstract

Previous data have suggested that glucocorticoids (GCs) are involved in the differentiation of thymocytes into mature T cells. In this report we demonstrate that the mouse thymic epithelial cells (TEC) express the cytochrome P450 hydroxylases Cyp11A1, Cyp21, and Cyp11B1. These enzymes, in combination with 3beta-hydroxysteroid dehydrogenase (3betaHSD), convert cholesterol into corticosterone, the major GC in rodents. In addition, when TEC were cocultured with 'reporter cells' containing the glucocorticoid receptor (GR) and a GR-dependent reporter gene, a specific induction of reporter gene activity was observed. Induction of reporter gene activity was blocked when the TEC and reporter cells were incubated in the presence of the Cyp11B1 inhibitor metyrapone or the 3betaHSD inhibitor trilostane, as well as by the GR antagonist RU486. Coculturing of TEC with thymocytes induced apoptosis in the latter, which was partially blocked by the enzyme inhibitors and RU486. We conclude that TEC secrete a GC hormone activity and suggest a paracrine role for this in thymocyte development.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3-Hydroxysteroid Dehydrogenases / metabolism
  • Animals
  • Apoptosis
  • Base Sequence
  • COS Cells
  • Cell Differentiation
  • Cholesterol Side-Chain Cleavage Enzyme / genetics
  • Cholesterol Side-Chain Cleavage Enzyme / metabolism
  • Coculture Techniques
  • DNA Primers / genetics
  • Epithelial Cells / cytology
  • Epithelial Cells / metabolism
  • Gene Expression
  • Genes, Reporter
  • Glucocorticoids / biosynthesis*
  • Luciferases / genetics
  • Mice
  • Mice, Inbred BALB C
  • Paracrine Communication / physiology*
  • Receptors, Glucocorticoid / metabolism
  • Steroid 11-beta-Hydroxylase / genetics
  • Steroid 11-beta-Hydroxylase / metabolism
  • Steroid 21-Hydroxylase / genetics
  • Steroid 21-Hydroxylase / metabolism
  • Thymus Gland / cytology
  • Thymus Gland / metabolism*

Substances

  • DNA Primers
  • Glucocorticoids
  • Receptors, Glucocorticoid
  • 3-Hydroxysteroid Dehydrogenases
  • Luciferases
  • Steroid 21-Hydroxylase
  • Steroid 11-beta-Hydroxylase
  • Cholesterol Side-Chain Cleavage Enzyme