Differential regulation of proto-oncogenes c-jun and c-fos in T lymphocytes activated through CD28

J Immunol. 1994 Dec 15;153(12):5393-401.

Abstract

The T cell surface molecule CD28 binds to ligands on accessory cells and APCs, playing an important costimulatory role in the response of T cells to Ags. Our knowledge of the intracellular signaling pathways coupled to this receptor is incomplete. In addition to activation of phospholipase C gamma 1, ligation of this receptor also seems to activate a calcium-independent, CD28-specific pathway. In this paper, we report that cross-linking of CD28 (but not CD2, CD5, LFA-1, or CD7) leads to an elevation of c-jun mRNA, with only minimal activation of c-fos expression. CD28-dependent induction of c-jun expression requires protein tyrosine kinase activity, but does not depend on activation of a phorbol ester-responsive protein kinase C or elevation of cytosolic calcium. Furthermore, CD28-dependent elevation of c-jun mRNA does not appear to be mediated at the level of mRNA stability. A mechanism is suggested whereby expression of c-jun and junB, in the absence of members of the fos family, can prevent inappropriate activation of T cells caused by ligation of CD28 in the absence of a specific antigenic stimulus.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Base Sequence
  • Benzoquinones
  • CD28 Antigens / genetics
  • CD28 Antigens / physiology*
  • Cells, Cultured
  • Dactinomycin / pharmacology
  • Egtazic Acid / pharmacology
  • Gene Expression Regulation / genetics
  • Humans
  • Ionomycin / pharmacology
  • Lactams, Macrocyclic
  • Lymphocyte Activation / genetics
  • Molecular Sequence Data
  • Proto-Oncogene Proteins c-fos / biosynthesis*
  • Proto-Oncogene Proteins c-fos / genetics
  • Proto-Oncogene Proteins c-jun / biosynthesis*
  • Proto-Oncogene Proteins c-jun / genetics
  • Quinones / pharmacology
  • Rifabutin / analogs & derivatives
  • Signal Transduction / genetics
  • T-Lymphocytes / immunology
  • T-Lymphocytes / metabolism*
  • Tetradecanoylphorbol Acetate / pharmacology

Substances

  • Benzoquinones
  • CD28 Antigens
  • Lactams, Macrocyclic
  • Proto-Oncogene Proteins c-fos
  • Proto-Oncogene Proteins c-jun
  • Quinones
  • Dactinomycin
  • Rifabutin
  • Egtazic Acid
  • Ionomycin
  • herbimycin
  • Tetradecanoylphorbol Acetate