Decreased SAP Expression in T Cells from Patients with Systemic Lupus Erythematosus Contributes to Early Signaling Abnormalities and Reduced IL-2 Production

J Immunol. 2016 Jun 15;196(12):4915-24. doi: 10.4049/jimmunol.1501523. Epub 2016 May 11.

Abstract

T cells from patients with systemic lupus erythematosus (SLE) display a number of abnormalities, including increased early signaling events following engagement of the TCR. Signaling lymphocytic activation molecule family cell surface receptors and the X-chromosome-defined signaling lymphocytic activation molecule-associated protein (SAP) adaptor are important in the development of several immunocyte lineages and modulating the immune response. We present evidence that SAP protein levels are decreased in T cells and in their main subsets isolated from 32 women and three men with SLE, independent of disease activity. In SLE T cells, SAP protein is also subject to increased degradation by caspase-3. Forced expression of SAP in SLE T cells normalized IL-2 production, calcium (Ca(2+)) responses, and tyrosine phosphorylation of a number of proteins. Exposure of normal T cells to SLE serum IgG, known to contain anti-CD3/TCR Abs, resulted in SAP downregulation. We conclude that SLE T cells display reduced levels of the adaptor protein SAP, probably as a result of continuous T cell activation and degradation by caspase-3. Restoration of SAP levels in SLE T cells corrects the overexcitable lupus T cell phenotype.

Publication types

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

MeSH terms

  • Adult
  • Aged
  • Calcium / metabolism
  • Caspase 3 / metabolism
  • Down-Regulation
  • Female
  • Humans
  • Immunoglobulin G / immunology
  • Interleukin-2 / biosynthesis*
  • Interleukin-2 / immunology
  • Lupus Erythematosus, Systemic / blood
  • Lupus Erythematosus, Systemic / immunology*
  • Lupus Erythematosus, Systemic / physiopathology
  • Lymphocyte Activation*
  • Male
  • Middle Aged
  • Phosphorylation
  • Receptors, Antigen, T-Cell / immunology
  • Signal Transduction*
  • Signaling Lymphocytic Activation Molecule Associated Protein / genetics
  • Signaling Lymphocytic Activation Molecule Associated Protein / metabolism*
  • Signaling Lymphocytic Activation Molecule Family / genetics
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / metabolism
  • Tyrosine / metabolism
  • Young Adult

Substances

  • Immunoglobulin G
  • Interleukin-2
  • Receptors, Antigen, T-Cell
  • SH2D1A protein, human
  • Signaling Lymphocytic Activation Molecule Associated Protein
  • Signaling Lymphocytic Activation Molecule Family
  • Tyrosine
  • Caspase 3
  • Calcium