PGE2-induced cyclic AMP accumulation in human CD4+ T cells is strongly enhanced during the CD2-mediated activatory process

Biochem Biophys Res Commun. 1988 Dec 30;157(3):1396-402. doi: 10.1016/s0006-291x(88)81030-1.

Abstract

The effect of a mitogenic combination of two different anti-CD2 monoclonal antibodies on the PGE2-stimulated and basal cAMP production in human CD4+ T cell clones was investigated. The anti-CD2 stimulation strongly potentiates the PGE2-induced cAMP production while both PMA and A23187 produced a less potent effect. On the opposite the anti-CD2 treatment is without any effect on the basal cAMP level contrasting with a marked increase of intracellular cAMP concentrations with A23187 or the combination of A23187 and PMA. These results suggest that activation of CD4+ human T cells via the CD2 molecule significantly influences the cAMP-related transduction pathway. Although PMA and A23187 also modulate the activity of this pathway, their effect in this model is more likely mediated through an amplification of basal cAMP production.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Monoclonal
  • Calcimycin / pharmacology
  • Calcium / metabolism
  • Calcium / pharmacology
  • Colforsin / pharmacology
  • Cyclic AMP / biosynthesis*
  • Dinoprostone / pharmacology*
  • Humans
  • Isoproterenol / pharmacology
  • Lymphocyte Activation* / drug effects
  • Protein Kinase C / metabolism
  • Receptors, Antigen, T-Cell / immunology
  • Receptors, Antigen, T-Cell / physiology*
  • T-Lymphocytes, Helper-Inducer / drug effects
  • T-Lymphocytes, Helper-Inducer / physiology*
  • Tetradecanoylphorbol Acetate / pharmacology

Substances

  • Antibodies, Monoclonal
  • Receptors, Antigen, T-Cell
  • Colforsin
  • Calcimycin
  • Cyclic AMP
  • Protein Kinase C
  • Dinoprostone
  • Isoproterenol
  • Tetradecanoylphorbol Acetate
  • Calcium