Effect of redox balance alterations on cellular localization of LAT and downstream T-cell receptor signaling pathways

Mol Cell Biol. 2002 Jan;22(2):400-11. doi: 10.1128/MCB.22.2.400-411.2002.

Abstract

The integral membrane protein linker for activation of T cells (LAT) is a central adapter protein in the T-cell receptor (TCR)-mediated signaling pathways. The cellular localization of LAT is extremely sensitive to intracellular redox balance alterations. Reduced intracellular levels of the antioxidant glutathione (GSH), a hallmark of chronic oxidative stress, resulted in the membrane displacement of LAT, abrogated TCR-mediated signaling and consequently hyporesponsiveness of T lymphocytes. The membrane displacement of LAT is accompanied by a considerable difference in the mobility of LAT upon native and nonreducing denaturing polyacrylamide gel electrophoresis analysis, a finding indicative of a conformational change. Targeted mutation of redox-sensitive cysteine residues within LAT created LAT mutants which remain membrane anchored under conditions of chronic oxidative stress. The expression of redox-insensitive LAT mutants allows for restoration of TCR-mediated signal transduction, whereas CD28-mediated signaling pathways remained impaired. These results are indicative that the membrane displacement of LAT as a result of redox balance alterations is a consequence of a conformational change interfering with the insertion of LAT into the plasma membrane. Conclusively, the data suggest a role for LAT as a crucial intermediate in the sensitivity of TCR signaling and hence T lymphocytes toward chronic oxidative stress.

MeSH terms

  • Adaptor Proteins, Signal Transducing*
  • Amino Acid Substitution
  • CD28 Antigens / metabolism
  • Carrier Proteins / chemistry
  • Carrier Proteins / genetics
  • Carrier Proteins / immunology*
  • Carrier Proteins / metabolism*
  • Cell Membrane / metabolism
  • Gene Expression
  • Humans
  • In Vitro Techniques
  • Interleukin-2 / genetics
  • Jurkat Cells
  • Lymphocyte Activation
  • Membrane Microdomains / metabolism
  • Membrane Proteins*
  • Models, Biological
  • Mutagenesis, Site-Directed
  • NF-kappa B / metabolism
  • Oxidation-Reduction
  • Oxidative Stress
  • Phosphoproteins / chemistry
  • Phosphoproteins / genetics
  • Phosphoproteins / immunology*
  • Phosphoproteins / metabolism*
  • Protein Conformation
  • Receptors, Antigen, T-Cell / metabolism*
  • Signal Transduction
  • Subcellular Fractions / metabolism
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / metabolism*
  • Transfection

Substances

  • Adaptor Proteins, Signal Transducing
  • CD28 Antigens
  • Carrier Proteins
  • Interleukin-2
  • LAT protein, human
  • Membrane Proteins
  • NF-kappa B
  • Phosphoproteins
  • Receptors, Antigen, T-Cell