Source:http://linkedlifedata.com/resource/pubmed/id/20421639
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
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pubmed:dateCreated |
2010-5-20
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pubmed:abstractText |
beta-Glucans are naturally occurring polysaccharides that are the major cell wall components of fungi. Recognition of beta-glucans is mediated through a membrane-bound pattern recognition receptor called dectin-1, and gene knock-out studies have shown that dectin-1 plays an important role in antifungal immune response in vivo. In this report, we have studied the effect of large particulate (1,3)-beta-glucans, including curdlan, glucan from baker's yeast, paramylon, and zymosan, on inflammatory response in human macrophages. We show that beta-glucans activate the transcription of the proinflammatory cytokine IL-1beta through a dectin-1-dependent pathway in human macrophages. Moreover, dectin-1 receptor associated Syk tyrosine kinase was essential for beta-glucan induced IL-1beta mRNA expression. In contrast to LPS, beta-glucans also strongly activated the secretion of IL-1beta. This beta-glucan triggered IL-1beta release was abolished by cytochalasin D, an inhibitor of phagocytosis, demonstrating that cytosolic recognition of beta-glucans is required for IL-1beta response in human macrophages. RNA interference-mediated gene knockdown experiments demonstrated that cytoplasmic NLRP3 inflammasome is essential for beta-glucan-induced IL-1beta secretion. Moreover, our results suggest that beta-glucan-induced NLRP3 inflammasome activation is dependent on the dectin-1/Syk signaling pathway. Furthermore, our results suggest that the lysosomal cathepsin B protease, the formation of reactive oxygen species, and the efflux of potassium are needed for beta-glucan-induced NLRP3 inflammasome activation. In conclusion, our results show that beta-glucans are recognized by membrane-associated dectin-1 and cytoplasmic NLRP3 inflammasome resulting in IL-1beta gene transcription and IL-1beta secretion in human macrophages, respectively.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Fungal Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-1beta,
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/NLRP3 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Nerve Tissue Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/beta-Glucans,
http://linkedlifedata.com/resource/pubmed/chemical/dectin 1
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1550-6606
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
1
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pubmed:volume |
184
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
6335-42
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pubmed:meshHeading |
pubmed-meshheading:20421639-Blotting, Western,
pubmed-meshheading:20421639-Carrier Proteins,
pubmed-meshheading:20421639-Enzyme-Linked Immunosorbent Assay,
pubmed-meshheading:20421639-Fungal Proteins,
pubmed-meshheading:20421639-Gene Expression,
pubmed-meshheading:20421639-Gene Expression Regulation,
pubmed-meshheading:20421639-Humans,
pubmed-meshheading:20421639-Interleukin-1beta,
pubmed-meshheading:20421639-Macrophage Activation,
pubmed-meshheading:20421639-Macrophages,
pubmed-meshheading:20421639-Membrane Proteins,
pubmed-meshheading:20421639-Nerve Tissue Proteins,
pubmed-meshheading:20421639-RNA Interference,
pubmed-meshheading:20421639-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:20421639-Signal Transduction,
pubmed-meshheading:20421639-beta-Glucans
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pubmed:year |
2010
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pubmed:articleTitle |
(1,3)-beta-glucans activate both dectin-1 and NLRP3 inflammasome in human macrophages.
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pubmed:affiliation |
Unit of Excellence for Immunotoxicology, Finnish Institute of Occupational Health, Helsinki, Finland.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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