Li Wei, Sofi M Hanief, Wei Datsen G, Du Wenjun, Gervay-Hague Jacquelyn, Renukaradhya Gourapura J, Brutkiewicz Randy R, Chang Cheong-Hee
Department of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, IN, USA.
Immunol Cell Biol. 2009 Feb;87(2):186-9. doi: 10.1038/icb.2008.78. Epub 2008 Nov 4.
Natural killer T (NKT) cells are positively selected on cortical thymocytes expressing the non-classical major histocompatibility complex (MHC) class I CD1d molecules. However, it is less clear how NKT cells are negatively selected in the thymus. In this study, we investigated the role of MHC class II expression in NKT cell development. Transgenic mice expressing MHC class II on thymocytes and peripheral T cells had a marked reduction in invariant NKT (iNKT) cells. Reduced numbers of iNKT cells correlated with the absence of in vivo production of cytokines in response to the iNKT cell agonist alpha-galactosylceramide. Using mixed bone marrow chimeras, we found that MHC class II-expressing thymocytes suppressed the development of iNKT cells in trans in a CD4-dependent manner. Our observations have significant implications for human iNKT cell development as human thymocytes express MHC class II, which can lead to an inefficient selection of iNKT cells.
自然杀伤T(NKT)细胞在表达非经典主要组织相容性复合体(MHC)I类分子CD1d的皮质胸腺细胞上进行阳性选择。然而,NKT细胞在胸腺中如何进行阴性选择尚不清楚。在本研究中,我们调查了MHC II类表达在NKT细胞发育中的作用。在胸腺细胞和外周T细胞上表达MHC II类的转基因小鼠中,恒定自然杀伤T(iNKT)细胞显著减少。iNKT细胞数量减少与体内对iNKT细胞激动剂α-半乳糖神经酰胺无细胞因子产生相关。使用混合骨髓嵌合体,我们发现表达MHC II类的胸腺细胞以CD4依赖的方式反式抑制iNKT细胞的发育。我们的观察结果对人类iNKT细胞发育具有重要意义,因为人类胸腺细胞表达MHC II类,这可能导致iNKT细胞选择效率低下。