Bosselut R, Feigenbaum L, Sharrow S O, Singer A
Experimental Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Immunity. 2001 Apr;14(4):483-94. doi: 10.1016/s1074-7613(01)00128-5.
The present study has assessed the impact of the intracellular domains of CD4 and CD8 on positive selection and lineage direction of MHC class I-restricted thymocytes. Contrary to current presumption, we found that the CD4 tail promotes the generation of both CD4+ and CD8+ T cells without preference for the CD4+ T cell lineage. We also found that the identity of the coreceptor tail and hence the strength of coreceptor signaling determine the number of thymocytes undergoing positive selection but not their ultimate CD4/CD8 phenotype. These findings demonstrate that the strength of coreceptor signaling has a significant quantitative but not qualitative impact on positive selection and provide a simple explanation for the greater numbers of CD4+ than CD8+ T cells selected in the normal thymus.
本研究评估了CD4和CD8的细胞内结构域对MHC I类限制性胸腺细胞阳性选择和谱系定向的影响。与当前推测相反,我们发现CD4尾促进CD4+和CD8+ T细胞的产生,而不偏向CD4+ T细胞谱系。我们还发现,共受体尾的特性以及共受体信号的强度决定了经历阳性选择的胸腺细胞数量,但不决定其最终的CD4/CD8表型。这些发现表明,共受体信号强度对阳性选择有显著的定量而非定性影响,并为正常胸腺中选择的CD4+ T细胞数量多于CD8+ T细胞提供了一个简单的解释。