Activation of T cell calcium influx by the second messenger ADP-ribose

J Biol Chem. 2006 Feb 3;281(5):2489-96. doi: 10.1074/jbc.M506525200. Epub 2005 Nov 29.

Abstract

Stimulation of Jurkat T cells by high concentrations of concanavalin A (ConA) induced an elevation of the endogenous adenosine diphosphoribose (ADPR) concentration and an inward current significantly different from the Ca2+ release-activated Ca2+ current (I(CRAC)). Electrophysiological characterization and activation of a similar current by infusion of ADPR indicated that the ConA-induced current is carried by TRPM2. Expression of TRPM2 in the plasma membrane of Jurkat T cells was demonstrated by reverse transcription-PCR, Western blot, and immunofluorescence. Inhibition of ADPR formation reduced ConA-mediated, but not store-operated, Ca2+ entry and prevented ConA-induced cell death of Jurkat cells. Moreover, gene silencing of TRPM2 abolished the ADPR- and ConA-mediated inward current. Thus, ADPR is a novel second messenger significantly involved in ConA-mediated cell death in T cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Diphosphate Ribose / metabolism*
  • Adenosine Diphosphate Ribose / physiology*
  • Calcium / metabolism*
  • Cell Death
  • Concanavalin A / pharmacology
  • Electrophysiology
  • Humans
  • Jurkat Cells
  • Lymphocyte Activation / drug effects
  • Second Messenger Systems / physiology*
  • T-Lymphocytes / metabolism*
  • TRPM Cation Channels / analysis
  • TRPM Cation Channels / genetics
  • TRPM Cation Channels / metabolism

Substances

  • TRPM Cation Channels
  • TRPM2 protein, human
  • Concanavalin A
  • Adenosine Diphosphate Ribose
  • Calcium