Nuclear appearance of a factor that binds the CD28 response element within the interleukin-2 enhancer correlates with interleukin-2 production

J Biol Chem. 1996 Apr 5;271(14):8321-7. doi: 10.1074/jbc.271.14.8321.

Abstract

Activation of T lymphocytes requires the combined signaling of the T cell receptor and costimulatory molecules such as CD28. The ability of T cells to produce interleukin-2 (IL-2) is a critical control point in T lymphocyte activation. The IL-2 enhancer contains a functional motif named CD28 response element (CD28RE) that serves a role as a target for mitogenic T cell activation signals. The CD28RE sequence reveals similarity to the consensus kappaB binding motif. Here we demonstrate that CD28RE binds an inducible protein with a molecular mass of approximately 35 kDa called nuclear factor of mitogenic-activated T cells (NF-MATp35) that is clearly different from the known NF- kappaB/Rel family members. Induction of NF-MATp35 was shown to depend on de novo protein synthesis and was restricted to T cells that received a mitogenic combination of T cell stimuli, not necessarily including CD28 signaling. Nonmitogenic T cell stimulation did not result in appearance of NF-MATp35. These results indicate that mitogenic combinations of T cell activation signals are integrated at the level of NF-MATp35 induction. Similar to its effect on IL-2 production, cyclosporin A inhibited the induction of NF-MATp35. Taken together, these data demonstrate that the nuclear appearance of NF-MATp35 shows excellent correlation with IL-2 production, which is a unique characteristic among nuclear factors implicated in the control of IL-2 gene expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • CD28 Antigens / metabolism*
  • Consensus Sequence
  • Cross-Linking Reagents
  • Cycloheximide / pharmacology
  • Cyclosporine / pharmacology
  • DNA-Binding Proteins / metabolism
  • Enhancer Elements, Genetic*
  • Gene Expression Regulation
  • Gene Expression Regulation, Viral
  • HIV-1 / genetics
  • Humans
  • Interleukin-2 / genetics*
  • Molecular Weight
  • NF-kappa B / metabolism
  • Nuclear Proteins / metabolism*
  • T-Lymphocytes / metabolism*
  • Transcription Factors / metabolism*
  • Tumor Cells, Cultured

Substances

  • CD28 Antigens
  • Cross-Linking Reagents
  • DNA-Binding Proteins
  • Interleukin-2
  • NF-kappa B
  • Nuclear Proteins
  • Transcription Factors
  • Cyclosporine
  • Cycloheximide