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不变自然杀伤 T 细胞识别微生物危险信号诱导的脂质自身抗原。

Invariant natural killer T cells recognize lipid self antigen induced by microbial danger signals.

机构信息

Department of Medicine, Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.

出版信息

Nat Immunol. 2011 Oct 30;12(12):1202-11. doi: 10.1038/ni.2143.

Abstract

Invariant natural killer T cells (iNKT cells) have a prominent role during infection and other inflammatory processes, and these cells can be activated through their T cell antigen receptors by microbial lipid antigens. However, increasing evidence shows that they are also activated in situations in which foreign lipid antigens would not be present, which suggests a role for lipid self antigen. We found that an abundant endogenous lipid, β-D-glucopyranosylceramide (β-GlcCer), was a potent iNKT cell self antigen in mouse and human and that its activity depended on the composition of the N-acyl chain. Furthermore, β-GlcCer accumulated during infection and in response to Toll-like receptor agonists, contributing to iNKT cell activation. Thus, we propose that recognition of β-GlcCer by the invariant T cell antigen receptor translates innate danger signals into iNKT cell activation.

摘要

固有自然杀伤 T 细胞(iNKT 细胞)在感染和其他炎症过程中起着重要作用,这些细胞可以通过其 T 细胞抗原受体被微生物脂质抗原激活。然而,越来越多的证据表明,它们在不存在外来脂质抗原的情况下也会被激活,这表明脂质自身抗原发挥了作用。我们发现一种丰富的内源性脂质,β-D-吡喃葡萄糖脑苷脂(β-GlcCer),是小鼠和人类中 iNKT 细胞的有效自身抗原,其活性取决于 N-酰基链的组成。此外,β-GlcCer 在感染期间和对 Toll 样受体激动剂的反应中积累,有助于 iNKT 细胞的激活。因此,我们提出,不变 T 细胞抗原受体对β-GlcCer 的识别将先天危险信号转化为 iNKT 细胞的激活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26cb/3242449/c19ce1ad3331/nihms326673f1.jpg

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