Post-transcriptional regulation of early T cell development by T cell receptor signals

Science. 1992 Nov 27;258(5087):1456-62. doi: 10.1126/science.1439838.

Abstract

During differentiation in the thymus, immature T cells progress through an ordered sequence of developmental stages that are best characterized by variable expression of the co-receptor molecules CD4 and CD8. Crosslinking of T cell receptor (TCR) molecules on precursor thymocytes was found to block their differentiation into CD4+CD8+ cells by eliminating messenger RNA's encoding two families of developmentally important molecules: the co-receptor molecules CD4 and CD8 and the recombination activating genes 1 and 2. TCR-induced post-transcriptional regulation in early thymocytes was specific for selective messenger RNA's, required protein synthesis, and was itself developmentally regulated. These data identify a post-transcriptional mechanism that is influenced by TCR signals and that regulates early thymocyte development.

MeSH terms

  • Animals
  • CD4 Antigens / genetics
  • CD8 Antigens / genetics
  • Cell Differentiation / physiology
  • Cells, Cultured
  • Fetus / cytology
  • Gene Rearrangement, T-Lymphocyte / genetics
  • Genes, RAG-1 / genetics
  • Mice
  • Protein Synthesis Inhibitors / pharmacology
  • Protein-Tyrosine Kinases / genetics
  • RNA Processing, Post-Transcriptional / physiology
  • RNA, Messenger / metabolism
  • Receptors, Antigen, T-Cell, alpha-beta / genetics
  • Receptors, Antigen, T-Cell, alpha-beta / physiology*
  • Signal Transduction / physiology
  • T-Lymphocytes / cytology*
  • T-Lymphocytes / drug effects
  • Tetradecanoylphorbol Acetate / pharmacology
  • Thymus Gland / cytology
  • Thymus Gland / embryology

Substances

  • CD4 Antigens
  • CD8 Antigens
  • Protein Synthesis Inhibitors
  • RNA, Messenger
  • Receptors, Antigen, T-Cell, alpha-beta
  • Protein-Tyrosine Kinases
  • Tetradecanoylphorbol Acetate