Wednesday, July 16, 2008 10:58:00 AM
FEMS Microbiol Lett. 2006 Nov 1
Trypanosoma cruzi exposes phosphatidylserine as an evasion mechanism.
Damatta RA, Seabra SH, Deolindo P, Arnholdt AC, Manhaes L, Goldenberg S, de Souza W.
Laboratorio de Biologia Celular e Tecidual, Universidad Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Chagas disease is caused by Trypanosoma cruzi and affects 18 million people in Central and South America. Here we analyzed the exposure of phosphatidylserine by the different forms of the parasite life cycle. Only the infective trypomastigotes, but not the epimastigotes or intracellular amastigotes, expose this phospholipid. This triggers a transforming growth factor beta signaling pathway, based on phosphorylated Smad 2 nuclear translocation, leading to iNOS disappearance in infected macrophages This macrophage deactivation favors the survival of this intracellular parasite. Thus, phosphatidylserine exposure may be used by T. cruzi to evade innate immunity and be a common feature of obligate intracellular parasites that have to deal with activated macrophages.
FULL PAPER:
http://www.blackwell-synergy.com/doi/full/10.1111/j.1574-6968.2006.00495.x?cookieSet=1
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