ζ Phosphorylation Without ZAP-70 Activation Induced by TCR Antagonists or Partial Agonists

Joaquı́n Madrenas(National Institute of Allergy and Infectious Diseases), Ronald L. Wange(National Institutes of Health), Jennifer L. Wang(National Institute of Allergy and Infectious Diseases), Noah Isakov(National Institutes of Health), Lawrence E. Samelson(National Institutes of Health), Ronald N. Germain(National Institute of Allergy and Infectious Diseases)
Science
January 27, 1995
Cited by 502

Abstract

Small changes in the peptide-major histocompatibility complex (MHC) molecule ligands recognized by antigen-specific T cell receptors (TCRs) can convert fully activating complexes into partially activating or even inhibitory ones. This study examined early TCR-dependent signals induced by such partial agonists or antagonists. In contrast to typical agonist ligands, both an antagonist and several partial agonists stimulated a distinct pattern of zeta chain phosphorylation and failed to activate associated ZAP-70 kinase. These results identify a specific step in the early tyrosine phosphorylation cascade that is altered after TCR engagement with modified peptide-MHC molecule complexes. This finding may explain the different biological responses to TCR occupancy by these variant ligands.


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