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Article
Inhibition of chlamydial infectious activity due to P2X7 receptor-dependent phospholipase D activation
Immunity
  • Robson Coutinho-Silva, Universidade Federal do Rio de Janeiro
  • Lynn Stahl, Universite Paris
  • Marie-Noelle Raymond, Universite Paris-Sud
  • Thomas Jungas, Universite Paris
  • Geoffrey Burnstock, Royal Free and University College
  • Toni Darville, University of Arkansas for Medical Sciences
  • David M. Ojcius, Universite Paris
  • Philippe Verbeke, Universite Paris
ORCiD
David M. Ojcius: 0000-0003-1461-4495
Document Type
Article
DOI
10.1016/S1074-7613(03)00235-8
Publication Date
9-1-2003
Abstract
Chlamydia trachomatis survives within host cells by inhibiting fusion between Chlamydia vacuoles and lysosomes. We show here that treatment of infected macrophages with ATP leads to killing of chlamydiae through ligation of the purinergic receptor, P2X7R. Chlamydial killing required phospholipase D (PLD) activation, as PLD inhibition led to rescue of chlamydiae in ATP-treated macrophages. However, there was no PLD activation nor chlamydial killing in ATP-treated P2X7R-deficient macrophages. P2X7R ligation exerts its effects by promoting fusion between Chlamydia vacuoles and lysosomes. P2X7R stimulation also resulted in macrophage death, but fusion with lysosomes preceded macrophage death and PLD inhibition did not prevent macrophage death. These results suggest that P2X7R ligation leads to PLD activation, which is directly responsible for inhibition of infection.
Citation Information
Robson Coutinho-Silva, Lynn Stahl, Marie-Noelle Raymond, Thomas Jungas, et al.. "Inhibition of chlamydial infectious activity due to P2X7 receptor-dependent phospholipase D activation" Immunity Vol. 19 Iss. 3 (2003) p. 403 - 412 ISSN: 1074-7613
Available at: http://works.bepress.com/david-ojcius/128/