| Literature DB >> 30352847 |
Takashi Imai1,2,3, Takayuki Matsumura4, Sabine Mayer-Lambertz5, Christine A Wells6, Eri Ishikawa2,7, Suzanne K Butcher6, Timothy C Barnett8,9, Mark J Walker8,9, Akihiro Imamura10, Hideharu Ishida11,12, Tadayoshi Ikebe13, Tomofumi Miyamoto14, Manabu Ato4, Shouichi Ohga3, Bernd Lepenies5, Nina M van Sorge15, Sho Yamasaki16,2,7,17.
Abstract
Group A Streptococcus (GAS) is a Gram-positive bacterial pathogen that causes a range of diseases, including fatal invasive infections. However, the mechanisms by which the innate immune system recognizes GAS are not well understood. We herein report that the C-type lectin receptor macrophage inducible C-type lectin (Mincle) recognizes GAS and initiates antibacterial immunity. Gene expression analysis of myeloid cells upon GAS stimulation revealed the contribution of the caspase recruitment domain-containing protein 9 (CARD9) pathway to the antibacterial responses. Among receptors signaling through CARD9, Mincle induced the production of inflammatory cytokines, inducible nitric oxide synthase, and reactive oxygen species upon recognition of the anchor of lipoteichoic acid, monoglucosyldiacylglycerol (MGDG), produced by GAS. Upon GAS infection, Mincle-deficient mice exhibited impaired production of proinflammatory cytokines, severe bacteremia, and rapid lethality. GAS also possesses another Mincle ligand, diglucosyldiacylglycerol; however, this glycolipid interfered with MGDG-induced activation. These results indicate that Mincle plays a central role in protective immunity against acute GAS infection.Entities:
Keywords: C-type lectin receptors; adjuvant; bacterial infection; glycolipids; innate immunity
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Year: 2018 PMID: 30352847 PMCID: PMC6233082 DOI: 10.1073/pnas.1809100115
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205