Ubiquitin-like protein MNSFβ negatively regulates T cell function and survival

Immunol Invest. 2015;44(1):1-12. doi: 10.3109/08820139.2014.909454. Epub 2014 Sep 2.

Abstract

Monoclonal non-specific suppressor factor β (MNSFβ) is a ubiquitously expressed member of the ubiquitin-like family that is involved in various biological functions. Previous studies have demonstrated that MNSFβ covalently binds to intracellular pro-apoptotic protein Bcl-G and regulates apoptosis in macrophages. In this study, we demonstrate that MNSFβ negatively regulates T cell function. In murine T-helper type 2 clone, D10.G4.1 (D10) cells transfected with MNSFβ cDNA, CD3/CD28-induced ERK1/2 phosphorylation leading to IL-4 production was significantly inhibited. The formation of MNSFβ-Bcl-G complex was induced by the CD3/CD28 stimulation. Co-transfection with MNSFβ and Bcl-G greatly enhanced CD3/CD28-induced apoptosis in D10 cells. Similarly, co-over-expression of MNSFβ and Bcl-G caused a marked enhancement of apoptosis in purified splenic T cells. Interestingly, this MNSFβ adduct was also induced in T cells derived from DO11.10 mice stimulated with antigen. Collectively, CD3/CD28-inducible MNSFβ-Bcl-G complex may be involved in the regulation of T cell function and survival.

Keywords: Bcl-G; ERK; T cell; ubiquitin-like protein.

MeSH terms

  • Animals
  • Antibodies, Monoclonal / pharmacology
  • Apoptosis
  • B-Lymphocytes / cytology
  • B-Lymphocytes / drug effects
  • B-Lymphocytes / metabolism
  • CD28 Antigens / genetics*
  • CD28 Antigens / metabolism
  • CD3 Complex / genetics*
  • CD3 Complex / metabolism
  • Cell Line
  • Cell Proliferation
  • Cell Survival
  • Gene Expression Regulation*
  • Interleukin-4 / biosynthesis
  • Interleukin-4 / metabolism
  • Mice
  • Mice, Inbred BALB C
  • Mitogen-Activated Protein Kinase 1 / genetics
  • Mitogen-Activated Protein Kinase 1 / metabolism
  • Mitogen-Activated Protein Kinase 3 / genetics
  • Mitogen-Activated Protein Kinase 3 / metabolism
  • Primary Cell Culture
  • Protein Binding
  • Proto-Oncogene Proteins c-bcl-2 / genetics*
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Signal Transduction
  • Spleen / cytology
  • Spleen / drug effects
  • Spleen / metabolism
  • Suppressor Factors, Immunologic / genetics*
  • Suppressor Factors, Immunologic / metabolism
  • T-Lymphocytes, Helper-Inducer / cytology
  • T-Lymphocytes, Helper-Inducer / drug effects
  • T-Lymphocytes, Helper-Inducer / metabolism*
  • Transfection

Substances

  • Antibodies, Monoclonal
  • BCL2L14 protein, mouse
  • CD28 Antigens
  • CD3 Complex
  • Proto-Oncogene Proteins c-bcl-2
  • Suppressor Factors, Immunologic
  • monoclonal nonspecific suppressor factor
  • Interleukin-4
  • Mitogen-Activated Protein Kinase 1
  • Mitogen-Activated Protein Kinase 3