Differential role of ICAM ligands in determination of human memory T cell differentiation

BMC Immunol. 2007 Jan 18:8:2. doi: 10.1186/1471-2172-8-2.

Abstract

Background: Leukocyte Function Antigen-1 (LFA-1) is a primary adhesion molecule that plays important roles in T cell activation, leukocyte recirculation, and trans-endothelial migration. By applying a multivariate intracellular phospho-proteomic analysis, we demonstrate that LFA-1 differentially activates signaling molecules.

Results: Signal intensity was dependent on both ICAM ligand and LFA-1 concentration. In the presence of CD3 and CD28 stimulation, ICAM-2 and ICAM-3 decreased TGFbeta1 production more than ICAM-1. In long-term differentiation experiments, stimulation with ICAM-3, CD3, and CD28 generated IFNgamma producing CD4+CD45RO+CD62L-CD11aBrightCD27- cells that had increased expression of intracellular BCL2, displayed distinct chemokine receptor profiles, and exhibited distinct migratory characteristics. Only CD3/CD28 with ICAM-3 generated CD4+CD45RO+CD62L-CD11aBrightCD27- cells that were functionally responsive to chemotaxis and exhibited higher frequencies of cells that signaled to JNK and ERK1/2 upon stimulation with MIP3alpha. Furthermore, these reports identify that the LFA-1 receptor, when presented with multiple ligands, can result in distinct T cell differentiation states and suggest that the combinatorial integration of ICAM ligand interactions with LFA-1 have functional consequences for T cell biology.

Conclusion: Thus, the ICAM ligands, differentially modulate LFA-1 signaling in T cells and potentiate the development of memory human T cells in vitro. These findings are of importance in a mechanistic understanding of memory cell differentiation and ex vivo generation of memory cell subsets for therapeutic applications.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • CD28 Antigens / immunology
  • CD28 Antigens / metabolism
  • CD3 Complex / immunology
  • CD3 Complex / metabolism
  • Caspase 3 / immunology
  • Caspase 3 / metabolism
  • Cell Adhesion Molecules / immunology*
  • Cell Differentiation / immunology*
  • Cells, Cultured
  • Flow Cytometry
  • Humans
  • Immunologic Memory*
  • Leukocyte Common Antigens / immunology
  • Leukocyte Common Antigens / metabolism
  • Ligands
  • Lymphocyte Activation / immunology
  • Lymphocyte Function-Associated Antigen-1 / immunology
  • Lymphocyte Function-Associated Antigen-1 / metabolism
  • T-Lymphocytes / cytology*
  • T-Lymphocytes / immunology*

Substances

  • CD28 Antigens
  • CD3 Complex
  • Cell Adhesion Molecules
  • Ligands
  • Lymphocyte Function-Associated Antigen-1
  • Leukocyte Common Antigens
  • Caspase 3