Selective CD28pYMNM mutations implicate phosphatidylinositol 3-kinase in CD86-CD28-mediated costimulation

Immunity. 1995 Oct;3(4):417-26. doi: 10.1016/1074-7613(95)90171-x.

Abstract

CD28 costimulatory signals are required for lymphokine production and T cell proliferation. CD28 signaling recruits the intracellular proteins PI 3-kinase, ITK, and GRB-2/SOS. PI 3-kinase and GRB-2/SOS bind the CD28 cytoplasmic pYMNM motif via SH2 domains. We generated CD28 pYMNM mutants and found that Y191 mutation (Y191CD28F) disrupted both PI 3-kinase and GRB-2 binding, while M194 mutation (M194CD28C) disrupted only PI 3-kinase binding. Both mutants still bound ITK. We have assessed the ability of these selective mutants to support IL-2 production upon TCR zeta/CD3 ligation in the presence of CHO-CD86 (B7-2) cells. Both Y191CD28F and M194CD28C mutants failed to generate IL-2. These data directly implicate PI 3-kinase in CD28-mediated costimulation leading to IL-2 secretion. Wortmannin, an inhibitor of PI 3-kinase, induced cell apoptosis and as such was unsuitable for use in this study.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD / immunology*
  • B7-2 Antigen
  • CD28 Antigens / genetics
  • CD28 Antigens / immunology*
  • CHO Cells
  • Cricetinae
  • Humans
  • Interleukin-2 / biosynthesis
  • Lymphocyte Activation / immunology*
  • Membrane Glycoproteins / immunology*
  • Mice
  • Mutation
  • Phosphatidylinositol 3-Kinases
  • Phosphotransferases (Alcohol Group Acceptor) / immunology*
  • Signal Transduction
  • T-Lymphocytes / immunology*

Substances

  • Antigens, CD
  • B7-2 Antigen
  • CD28 Antigens
  • CD86 protein, human
  • Cd86 protein, mouse
  • Interleukin-2
  • Membrane Glycoproteins
  • Phosphatidylinositol 3-Kinases
  • Phosphotransferases (Alcohol Group Acceptor)