The fungal ligand chitin directly binds TLR2 and triggers inflammation dependent on oligomer size.

Details

Serval ID
serval:BIB_DF9779D4CD31
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
The fungal ligand chitin directly binds TLR2 and triggers inflammation dependent on oligomer size.
Journal
EMBO reports
Author(s)
Fuchs K., Cardona Gloria Y., Wolz O.O., Herster F., Sharma L., Dillen C.A., Täumer C., Dickhöfer S., Bittner Z., Dang T.M., Singh A., Haischer D., Schlöffel M.A., Koymans K.J., Sanmuganantham T., Krach M., Roger T., Le Roy D., Schilling N.A., Frauhammer F., Miller L.S., Nürnberger T., LeibundGut-Landmann S., Gust A.A., Macek B., Frank M., Gouttefangeas C., Dela Cruz C.S., Hartl D., Weber A.N.
ISSN
1469-3178 (Electronic)
ISSN-L
1469-221X
Publication state
Published
Issued date
12/2018
Peer-reviewed
Oui
Volume
19
Number
12
Language
english
Notes
Publication types: Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Abstract
Chitin is the second most abundant polysaccharide in nature and linked to fungal infection and asthma. However, bona fide immune receptors directly binding chitin and signaling immune activation and inflammation have not been clearly identified because polymeric crude chitin with unknown purity and molecular composition has been used. By using defined chitin (N-acetyl-glucosamine) oligomers, we here identify six-subunit-long chitin chains as the smallest immunologically active motif and the innate immune receptor Toll-like receptor (TLR2) as a primary fungal chitin sensor on human and murine immune cells. Chitin oligomers directly bind TLR2 with nanomolar affinity, and this fungal TLR2 ligand shows overlapping and distinct signaling outcomes compared to known mycobacterial TLR2 ligands. Unexpectedly, chitin oligomers composed of five or less subunits are inactive, hinting to a size-dependent system of immuno-modulation that appears conserved in plants and humans. Since blocking of the chitin-TLR2 interaction effectively prevents chitin-mediated inflammation in vitro and in vivo, our study highlights the chitin-TLR2 interaction as a potential target for developing novel therapies in chitin-related pathologies and fungal disease.
Keywords
Animals, Cell Wall/drug effects, Cell Wall/metabolism, Chitin/chemistry, Chitin/metabolism, Chitinases/metabolism, Female, Fungi/metabolism, Humans, Hydrophobic and Hydrophilic Interactions, Immunologic Factors/pharmacology, Inflammation/metabolism, Inflammation/pathology, Ligands, Lymphocytes/drug effects, Lymphocytes/metabolism, Mice, Inbred C57BL, Mice, Knockout, THP-1 Cells, Toll-Like Receptor 1/agonists, Toll-Like Receptor 1/metabolism, Toll-Like Receptor 2/chemistry, Toll-Like Receptor 2/metabolism, Zymosan/metabolism, N‐acetyl‐glucosamine, anti‐fungal innate immunity, chitin, inflammation, toll‐like receptor
Pubmed
Web of science
Create date
29/10/2018 12:57
Last modification date
20/08/2019 16:04
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