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Fungal Chitin Reduces Platelet Activation Mediated via TLR8 Stimulation.

Authors :
Leroy J
Bortolus C
Lecointe K
Parny M
Charlet R
Sendid B
Jawhara S
Source :
Frontiers in cellular and infection microbiology [Front Cell Infect Microbiol] 2019 Nov 12; Vol. 9, pp. 383. Date of Electronic Publication: 2019 Nov 12 (Print Publication: 2019).
Publication Year :
2019

Abstract

Platelets play an important role in the innate immune response. During candidaemia, circulating fungal polysaccharides, including chitin, are released into the bloodstream and can interact with platelets and induce modulation of platelet activities. However, the role of circulating chitin in platelet modulation has not been investigated. The aims of the present study were to assess the effect of fungal chitin on activation, adhesion, aggregation and receptor expression of platelets and their impact on the host defense against Candida albicans . Platelets pre-treated with different concentrations of chitin (10-400 μg/mL) extracted from C. albicans were analyzed in terms of activation, Toll-like receptor (TLR) expression, aggregation and adhesion to C. albicans . Chitin treatment reduced platelet adhesion to C. albicans and neutrophils. P-selectin expression was significantly decreased in platelets challenged with chitin. Aggregation and intracellular Ca <superscript>2+</superscript> influx were also decreased in platelets. TLR8 mRNA and proteins were expressed in platelets pre-treated with chitin when compared to untreated platelets. Overall, chitin purified from C. albicans reduced the adhesion, activation and aggregation of platelets mediated via TLR8 stimulation by decreasing intracellular Ca <superscript>2+</superscript> influx and P-selectin expression.<br /> (Copyright © 2019 Leroy, Bortolus, Lecointe, Parny, Charlet, Sendid and Jawhara.)

Details

Language :
English
ISSN :
2235-2988
Volume :
9
Database :
MEDLINE
Journal :
Frontiers in cellular and infection microbiology
Publication Type :
Academic Journal
Accession number :
31781518
Full Text :
https://doi.org/10.3389/fcimb.2019.00383