Bendelac A, Killeen N, Littman D R, Schwartz R H
Laboratory of Cellular and Molecular Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892.
Science. 1994 Mar 25;263(5154):1774-8. doi: 10.1126/science.7907820.
To complete their maturation, most immature thymocytes depend on the simultaneous engagement of their antigen receptor [alpha beta T cell receptor (TCR)] and their CD4 or CD8 coreceptors with major histocompatibility complex class II or I ligands, respectively. However, a normal subset of mature alpha beta TCR+ thymocytes did not follow these rules. These thymocytes expressed NK1.1 and a restricted set of alpha beta TCRs that are intrinsically class I-reactive because their positive selection was class I-dependent but CD8-independent. These cells were CD4+ and CD4-8- but never CD8+, because the presence of CD8 caused negative selection. Thus, neither CD4 nor CD8 contributes signals that direct their maturation into the CD4+ and CD4-8- lineages.
为了完成其成熟过程,大多数未成熟胸腺细胞分别依赖于其抗原受体(αβ T细胞受体,TCR)与主要组织相容性复合体II类或I类配体同时结合其CD4或CD8共受体。然而,成熟的αβ TCR+胸腺细胞的一个正常亚群并不遵循这些规则。这些胸腺细胞表达NK1.1和一组受限的αβ TCR,这些TCR本质上对I类有反应性,因为它们的阳性选择依赖于I类但不依赖于CD8。这些细胞是CD4+和CD4-8-,但从不CD8+,因为CD8的存在会导致阴性选择。因此,CD4和CD8都不提供指导它们成熟为CD4+和CD4-8-谱系的信号。