Functional associations of CD38 with CD3 on the T-cell membrane

J Biol Regul Homeost Agents. 1997 Oct-Dec;11(4):137-42.

Abstract

CD38 is a multifunctional membrane surface glycoprotein expressed by different cells and tissues, including T cells at certain stages of their development. Besides its involvement in transmembrane signaling, CD38 play a role in cell adhesion processes. Structurally, membrane CD38 was reported as presenting lateral associations with molecules involved in recognition and signaling, namely with the TCR/CD3 complex in T cells. Here we report that ligation of CD38 by agonistic and non-agonistic monoclonal antibodies exerts different effects on T cells, the former inducing down-modulation of the associated molecules, probably through a protein kinase C-dependent mechanism. This observation supports the view that the reduced expression of TCR/CD3 is secondary to interplay with CD38-mediated signaling, which partially overlaps with the CD3-mediated pathway. CD3 ligation by monoclonal antibodies leads not only to the expected internalization of the TCR/CD3 complex but also to down-modulation of surface CD38. The results obtained indicate that CD38 is closely associated with the CD3/TCR complex and that co-modulation of CD38 with TCR/CD3 is a critical step in signaling processes on T lymphocytes.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • ADP-ribosyl Cyclase
  • ADP-ribosyl Cyclase 1
  • Antibodies, Monoclonal / immunology
  • Antigens, CD*
  • Antigens, Differentiation / analysis
  • Antigens, Differentiation / physiology*
  • Antigens, Neoplasm / analysis
  • Antigens, Neoplasm / physiology
  • CD3 Complex / analysis
  • CD3 Complex / physiology*
  • Cell Adhesion
  • Cell Membrane / physiology
  • Down-Regulation
  • Endocytosis
  • Enzyme Inhibitors / pharmacology
  • Humans
  • Immunoglobulin Fab Fragments / immunology
  • Jurkat Cells / chemistry
  • Jurkat Cells / physiology
  • Leukemia-Lymphoma, Adult T-Cell / pathology
  • Macromolecular Substances
  • Membrane Glycoproteins
  • NAD+ Nucleosidase / analysis
  • NAD+ Nucleosidase / physiology*
  • Protein Kinase C / antagonists & inhibitors
  • Protein Kinase C / physiology
  • Receptor-CD3 Complex, Antigen, T-Cell / immunology
  • Receptor-CD3 Complex, Antigen, T-Cell / physiology*
  • Signal Transduction / physiology*
  • Staurosporine / pharmacology
  • T-Lymphocytes / chemistry
  • T-Lymphocytes / physiology*
  • Tetradecanoylphorbol Acetate / pharmacology
  • Tumor Cells, Cultured

Substances

  • Antibodies, Monoclonal
  • Antigens, CD
  • Antigens, Differentiation
  • Antigens, Neoplasm
  • CD3 Complex
  • Enzyme Inhibitors
  • Immunoglobulin Fab Fragments
  • Macromolecular Substances
  • Membrane Glycoproteins
  • Receptor-CD3 Complex, Antigen, T-Cell
  • Protein Kinase C
  • ADP-ribosyl Cyclase
  • CD38 protein, human
  • NAD+ Nucleosidase
  • ADP-ribosyl Cyclase 1
  • Staurosporine
  • Tetradecanoylphorbol Acetate

Grants and funding