Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/40609
Title: Activation of invariant natural killer T cells stimulated with microbial α-mannosyl glycolipids.
Authors: Shimamura, Michio
Yamamura, Masaki
Nabeshima, Tatsuya
Kitano, Naoki
van den Elzen, Peter
Yesilkaya, Hasan
Andrew, Peter
Illarionov, Petr
First Published: 29-Aug-2017
Publisher: Nature Publishing Group
Citation: Scientific Reports, 2017, 7, Article number: 9703
Abstract: Some synthetic and bacterial glycolipids presented by CD1d specifically activate invariant NKT (iNKT) cells bearing an invariant Vα14-Jα18 (mouse) or Vα24-Jα18 (human) TCR. The antigenic glycolipids identified to date consist of two hydrophobic chains and an α-glycoside in which the 2′-OH group is in the cis orientation toward the anomeric group, namely, either an α-galactoside or an α-glucoside. Several microbial α-mannosyl glycolipids, in which the 2′-OH group is in the trans orientation, were herein examined to establish whether they have potential to activate iNKT cells. We found that α-mannnosyl1-3 (6′-O-acyl α-mannosyl)-1-1 monoacylglycerol and cholesteryl 6′-O-acyl α-mannoside, found in Saccharopolyspora and Candida albicans, respectively, induced the activation of iNKT cells, dependent on CD1d. In contrast, α-mannosyldiacylglycerol found in Streptococcus suis or α-mannosylceramide demonstrated markedly less antigenicity for iNKT cells. The potentially antigenic α-mannosyl glycolipids contributed to the protection of mice against infection with S. pneumoniae in which iNKT cells have previously been found to participate. Furthermore, these glycolipids induced the production of proinflammatory cytokines by macrophages, thereby suggesting their recognition by specific pattern recognition receptors (PRRs). Collectively, these results suggest that these microbial α-mannosyl glycolipids are capable of being recognized by both the invariant TCR and PRRs and inducing immune responses.
DOI Link: 10.1038/s41598-017-10309-x
ISSN: 2045-2322
eISSN: 2045-2322
Links: https://www.nature.com/articles/s41598-017-10309-x
http://hdl.handle.net/2381/40609
Version: Publisher Version
Status: Peer-reviewed
Type: Journal Article
Rights: Copyright © the authors, 2017. This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Description: Supplementary information accompanies this paper at doi:10.1038/s41598-017-10309-x
Appears in Collections:Published Articles, Dept. of Infection, Immunity and Inflammation

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