Department of Medicine, Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Nat Immunol. 2011 Oct 30;12(12):1202-11. doi: 10.1038/ni.2143.
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.
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。