Document Detail


TLR4 recognizes Pseudallescheria boydii conidia and purified rhamnomannans.
MedLine Citation:
PMID:  20959459     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Pseudallescheria boydii (Scedosporium apiospermum) is a saprophytic fungus widespread in the environment, and has recently emerged as an agent of localized as well as disseminated infections, particularly mycetoma, in immunocompromised and immunocompetent hosts. We have previously shown that highly purified α-glucan from P. boydii activates macrophages through Toll-like receptor TLR2, however, the mechanism of P. boydii recognition by macrophage is largely unknown. In this work, we investigated the role of innate immune receptors in the recognition of P. boydii. Macrophages responded to P. boydii conidia and hyphae with secretion of proinflammatory cytokines. The activation of macrophages by P. boydii conidia required functional MyD88, TLR4, and CD14, whereas stimulation by hyphae was independent of TLR4 and TLR2 signaling. Removal of peptidorhamnomannans from P. boydii conidia abolished induction of cytokines by macrophages. A fraction highly enriched in rhamnomannans was obtained and characterized by NMR, high performance TLC, and GC-MS. Preparation of rhamnomannans derived from P. boydii triggered cytokine release by macrophages, as well as MAPKs phosphorylation and IκBα degradation. Cytokine release induced by P. boydii-derived rhamnomannans was dependent on TLR4 recognition and required the presence of non-reducing end units of rhamnose of the rhamnomannan, but not O-linked oligosaccharides from the peptidorhamnomannan. These results imply that TLR4 recognizes P. boydii conidia and this recognition is at least in part due to rhamnomannans expressed on the surface of P. boydii.
Authors:
Rodrigo T Figueiredo; Patrícia L Fernandez; Fabianno F Dutra; Yissett González; Lívia Cristina Lopes; Vera Carolina B Bittencourt; Guilherme L Sassaki; Eliana Barreto-Bergter; Marcelo T Bozza
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2010-10-19
Journal Detail:
Title:  The Journal of biological chemistry     Volume:  285     ISSN:  1083-351X     ISO Abbreviation:  J. Biol. Chem.     Publication Date:  2010 Dec 
Date Detail:
Created Date:  2010-12-20     Completed Date:  2011-01-24     Revised Date:  2013-07-03    
Medline Journal Info:
Nlm Unique ID:  2985121R     Medline TA:  J Biol Chem     Country:  United States    
Other Details:
Languages:  eng     Pagination:  40714-23     Citation Subset:  IM    
Affiliation:
Departamento de Imunologia, Laboratório de Inflamação e Imunidade, Instituto de Microbiologia, Universidade Federal do Rio de Janeiro, Rio de Janeiro, 941-902 Brazil.
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MeSH Terms
Descriptor/Qualifier:
Animals
Antigens, CD14 / immunology,  metabolism
Cytokines / immunology,  secretion
Hyphae / immunology,  metabolism
Immunity, Innate / immunology
Macrophage Activation / immunology*
Macrophages, Peritoneal / immunology*,  metabolism
Mannans / immunology*,  metabolism
Mice
Mice, Knockout
Mitogen-Activated Protein Kinase Kinases / immunology,  metabolism
Myeloid Differentiation Factor 88 / immunology,  metabolism
Pseudallescheria / immunology*,  metabolism
Spores, Fungal / immunology*,  metabolism
Toll-Like Receptor 2 / immunology,  metabolism
Toll-Like Receptor 4 / immunology*,  metabolism
Chemical
Reg. No./Substance:
0/Antigens, CD14; 0/Cytokines; 0/Mannans; 0/Myd88 protein, mouse; 0/Myeloid Differentiation Factor 88; 0/Tlr2 protein, mouse; 0/Tlr4 protein, mouse; 0/Toll-Like Receptor 2; 0/Toll-Like Receptor 4; EC 2.7.12.2/Mitogen-Activated Protein Kinase Kinases
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