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T细胞以及模式识别受体MCL和Mincle对微生物糖脂及相关缀合物的免疫感应。

Immune sensing of microbial glycolipids and related conjugates by T cells and the pattern recognition receptors MCL and Mincle.

作者信息

Smith Dylan G M, Williams Spencer J

机构信息

School of Chemistry and Bio21 Molecular Science and Biotechnology Institute, University of Melbourne, Parkville 3010, Australia.

School of Chemistry and Bio21 Molecular Science and Biotechnology Institute, University of Melbourne, Parkville 3010, Australia.

出版信息

Carbohydr Res. 2016 Feb;420:32-45. doi: 10.1016/j.carres.2015.11.009. Epub 2015 Dec 8.

DOI:10.1016/j.carres.2015.11.009
PMID:26717547
Abstract

Microbes produce a wide range of small molecule glycoconjugates that constitute unique molecular signatures. These molecules are recognized by a range of detection systems, triggering immune responses to microbial pathogens and commensals. The antigen-presenting molecules of the CD1 class, CD1a-d, capture lipidic molecules and present them to diverse and innate-like T cell populations including natural killer T cells and germline-encoded mycolyl reactive T cells. The antigen-presenting molecule MR1 captures vitamin B metabolites and presents them to mucosal associated invariant T cells. In both cases, recognition of the small molecule-antigen presenting molecule complexes occurs through T cell receptors on the surface of T lymphocytes. The pattern recognition receptors macrophage C-type lectin (MCL) and macrophage inducible C-type lectin (Mincle) receptors sense glycolipids and through signalling initiate cellular activation, shaping immune responses to peptide antigens, including the differentiation of naïve T cells into conventional effector T helper cells. In this review, we provide an overview of the diverse structures of immunogenic lipidic molecules and vitamin B metabolites and their recognition by select systems of the immune system. Future advances in our understanding of the roles of such molecules in innate and adaptive immune responses will require the coordinated efforts of synthetic and natural products chemists, immunologists and biologists.

摘要

微生物产生多种构成独特分子特征的小分子糖缀合物。这些分子被一系列检测系统识别,引发对微生物病原体和共生菌的免疫反应。CD1类抗原呈递分子(CD1a - d)捕获脂质分子,并将它们呈递给包括自然杀伤T细胞和种系编码的分枝杆菌反应性T细胞在内的多种天然样T细胞群体。抗原呈递分子MR1捕获维生素B代谢产物,并将它们呈递给黏膜相关恒定T细胞。在这两种情况下,小分子 - 抗原呈递分子复合物的识别都是通过T淋巴细胞表面的T细胞受体发生的。模式识别受体巨噬细胞C型凝集素(MCL)和巨噬细胞诱导性C型凝集素(Mincle)受体感知糖脂,并通过信号传导启动细胞活化,塑造对肽抗原的免疫反应,包括将幼稚T细胞分化为传统效应性T辅助细胞。在本综述中,我们概述了免疫原性脂质分子和维生素B代谢产物的多样结构以及它们被免疫系统特定系统识别的情况。未来要进一步了解此类分子在固有免疫和适应性免疫反应中的作用,需要合成与天然产物化学家、免疫学家和生物学家的共同努力。

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