Document Detail


Host cell lipid bodies triggered by Trypanosoma cruzi infection and enhanced by the uptake of apoptotic cells are associated with prostaglandin E₂ generation and increased parasite growth.
MedLine Citation:
PMID:  21849292     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Lipid bodies (lipid droplets) are lipid-rich organelles with functions in cell metabolism and signaling. Here, we investigate the mechanisms of Trypanosoma cruzi-induced lipid body formation and their contributions to host-parasite interplay. We demonstrate that T. cruzi-induced lipid body formation in macrophages occurs in a Toll-like receptor 2-dependent mechanism and is potentiated by apoptotic cell uptake. Lipid body biogenesis and prostaglandin E₂ (PGE₂) production triggered by apoptotic cell uptake was largely dependent of α(v)β₃ and transforming growth factor-β signaling. T. cruzi-induced lipid bodies act as sites of increased PGE synthesis. Inhibition of lipid body biogenesis by the fatty acid synthase inhibitor C75 reversed the effects of apoptotic cells on lipid body formation, eicosanoid synthesis, and parasite replication. Our findings indicate that lipid bodies are highly regulated organelles during T. cruzi infection with roles in lipid mediator generation by macrophages and are potentially involved in T. cruzi-triggered escape mechanisms.
Authors:
Heloisa D'Avila; Célio G Freire-de-Lima; Natalia R Roque; Livia Teixeira; Christina Barja-Fidalgo; Adriana R Silva; Rossana C N Melo; George A Dosreis; Hugo C Castro-Faria-Neto; Patrícia T Bozza
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  The Journal of infectious diseases     Volume:  204     ISSN:  1537-6613     ISO Abbreviation:  J. Infect. Dis.     Publication Date:  2011 Sep 
Date Detail:
Created Date:  2011-08-18     Completed Date:  2011-10-13     Revised Date:  2011-10-31    
Medline Journal Info:
Nlm Unique ID:  0413675     Medline TA:  J Infect Dis     Country:  United States    
Other Details:
Languages:  eng     Pagination:  951-61     Citation Subset:  AIM; IM    
Affiliation:
Laboratório de Imunofarmacologia, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Rio de Janeiro, Brazil.
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MeSH Terms
Descriptor/Qualifier:
Animals
Chagas Disease / pathology*
Dinoprostone / metabolism*
Female
Host-Parasite Interactions*
Lipid Metabolism*
Macrophages / metabolism*,  parasitology*
Mice
Mice, Inbred C57BL
Rats
Rats, Sprague-Dawley
Toll-Like Receptor 2 / metabolism
Trypanosoma cruzi / growth & development,  pathogenicity*
Chemical
Reg. No./Substance:
0/Toll-Like Receptor 2; 363-24-6/Dinoprostone

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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