Regulation of expression of CD27, a T cell-specific member of a novel family of membrane receptors

J Immunol. 1991 Apr 15;146(8):2488-94.

Abstract

CD27 belongs to a newly defined family of transmembrane R, including the nerve growth factor R, two distinct TNF R and CD40. The function of CD27 is unknown, but on the basis of structural and functional properties, we postulate that it plays a role in the events subsequent to T cell activation, possibly as a cytokine R. We have analyzed the mechanisms underlying the regulation of CD27 protein expression. Membrane expression of CD27 strongly increases after T cell activation via the TCR/CD3 complex or the CD2 molecule. In contrast, direct stimulation of protein kinase C by phorbol esters markedly down-regulates CD27 surface expression. This down-regulation most likely does not result from CD27 phosphorylation, because both anti-CD3 mAb and PMA induce hyperphosphorylation of CD27 on serine residues. Rather, membrane expression seems to be regulated primarily at the RNA level. Stimulation of T cells with anti-CD3 mAb strongly increases steady state CD27 mRNA levels, whereas PMA treatment greatly reduces these transcript levels. Dissection of the TCR/CD3-induced signaling pathways showed that cytoplasmic cAMP as well as Ca2+ concentrations contribute to the increase of CD27 expression. These data indicate that upon Ag-specific T cell stimulation, membrane expression of CD27 is regulated at the RNA level through the joint action of distinct TCR/CD3-associated signaling pathways.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Monoclonal / pharmacology
  • Antigens, Differentiation, T-Lymphocyte / biosynthesis
  • Antigens, Differentiation, T-Lymphocyte / genetics*
  • Blotting, Northern
  • Bucladesine / pharmacology
  • Calcium / physiology
  • Cell Division
  • Colforsin / pharmacology
  • Cyclic AMP / physiology
  • Dose-Response Relationship, Drug
  • Down-Regulation
  • Electrophoresis, Polyacrylamide Gel
  • Fluorescent Antibody Technique
  • Gene Expression Regulation*
  • Humans
  • Lymphocyte Activation / drug effects
  • Lymphocyte Activation / physiology
  • Phosphorylation / drug effects
  • Phytohemagglutinins / pharmacology
  • Precipitin Tests
  • Protein Kinase C / biosynthesis
  • RNA / analysis
  • RNA / metabolism
  • Second Messenger Systems / physiology
  • T-Lymphocytes / immunology*
  • Tumor Necrosis Factor Receptor Superfamily, Member 7

Substances

  • Antibodies, Monoclonal
  • Antigens, Differentiation, T-Lymphocyte
  • Phytohemagglutinins
  • Tumor Necrosis Factor Receptor Superfamily, Member 7
  • Colforsin
  • RNA
  • Bucladesine
  • Cyclic AMP
  • Protein Kinase C
  • Calcium