T cell stimulation in the absence of exogenous antigen: a T cell signal is induced by both MHC-dependent and -independent mechanisms

Eur J Immunol. 2003 Nov;33(11):3109-16. doi: 10.1002/eji.200324067.

Abstract

Mature T cells residing in peripheral lymphoid organs have frequent contact with antigen presenting cells (APC). Such contact may be required for T cell survival, but the degree to which signals in mature T cells are induced by TCR recognition of self peptide/MHC complexes is unclear. We have used induction of the early growth response gene 1 (Egr1) as an indicator of signal transduction in 3.L2 (I-Ek-restricted) T cells interacting with APC in the absence of exogenous antigen. The data show that Egr1 can be induced in 3.L2 T cells by TCR recognition of self peptides presented by I-Ek. However, a more transient induction of Egr1 can be induced in 3.L2 T cells interacting with dendritic cells derived from class II/beta2m double-deficient mice. Egr1 induction after T cell-APC contact was also observed in a freshly isolated polyclonal CD4 T cell population. The data suggest that self peptide/MHC recognition by the TCR induces a signal in T cells and that dendritic cells can also induce a more transient T cell signal by an MHC-independent mechanism.

Publication types

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

MeSH terms

  • Animals
  • Antigen-Presenting Cells / physiology
  • Antigens / physiology
  • DNA-Binding Proteins / metabolism*
  • Early Growth Response Protein 1
  • Histocompatibility Antigens / physiology*
  • Immediate-Early Proteins*
  • Major Histocompatibility Complex / physiology
  • Mice
  • Peptides / metabolism
  • RNA, Messenger / metabolism*
  • T-Lymphocytes / physiology*
  • Transcription Factors / metabolism*

Substances

  • Antigens
  • DNA-Binding Proteins
  • Early Growth Response Protein 1
  • Egr1 protein, mouse
  • Histocompatibility Antigens
  • Immediate-Early Proteins
  • Peptides
  • RNA, Messenger
  • Transcription Factors