Differential remodeling of a T-cell transcriptome following CD8- versus CD3-induced signaling

Cell Res. 2008 Jun;18(6):641-8. doi: 10.1038/cr.2008.56.

Abstract

CD8 engagement with class I major histocompatibility antigens greatly enhances T-cell activation, but it is not clear how this is achieved. We address the question of whether or not the antibody-mediated ligation of CD8 alone induces transcriptional remodeling in a T-cell clone, using serial analysis of gene expression. Even though it fails to induce overt phenotypic changes, we find that CD8 ligation profoundly alters transcription in the T-cell clone, at a scale comparable to that induced by antibody-mediated ligation of CD3. The character of the resulting changes is distinct, however, with the net effect of CD8 ligation being substantially inhibitory. We speculate that ligating CD8 induces weak, T-cell receptor (TCR)-mediated inhibitory signals reminiscent of the effects of TCR antagonists. Our results imply that CD8 ligation alone is incapable of activating the T-cell clone because it fails to fully induce NFAT-dependent transcription.

Publication types

  • Comparative Study

MeSH terms

  • Antibodies / pharmacology
  • CD3 Complex / metabolism*
  • CD8 Antigens / metabolism*
  • Clone Cells
  • Gene Expression Profiling*
  • Gene Expression Regulation / drug effects
  • Gene Library
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Signal Transduction* / drug effects
  • T-Lymphocytes / drug effects
  • T-Lymphocytes / metabolism*

Substances

  • Antibodies
  • CD3 Complex
  • CD8 Antigens
  • RNA, Messenger