Robey E A, Fowlkes B J, Gordon J W, Kioussis D, von Boehmer H, Ramsdell F, Axel R
Department of Biochemistry and Molecular Biophysics, Columbia University, New York, New York 10032.
Cell. 1991 Jan 11;64(1):99-107. doi: 10.1016/0092-8674(91)90212-h.
Immature thymocytes, which coexpress CD4 and CD8, give rise to mature CD4+CD8- and CD4-CD8+ T cells. Only those T cells that recognize self-MHC are selected to mature, a process known as positive selection. The specificity of the T cell antigen receptor (TCR) for class I or class II MHC influences the commitment to a CD4 or CD8 lineage. This may occur by a directed mechanism or by stochastic commitment followed by a selection step that allows only CD8+, class I-specific and CD4+, class II-specific cells to survive. We have generated a mouse line expressing a CD8 transgene under the control of the T cell-specific CD2 regulatory sequences. Although constitutive CD8 expression does not affect thymic selection of CD4+ cells, selection of a class I-specific TCR in the CD8 subset is substantially improved. This outcome is consistent with a model for positive selection in which selection occurs at a developmental stage in which both CD4 and CD8 are expressed, and positive selection by class I MHC generates an instructive signal that directs differentiation to a CD8 lineage.
共表达CD4和CD8的未成熟胸腺细胞可分化为成熟的CD4+CD8-和CD4-CD8+ T细胞。只有那些识别自身MHC的T细胞才会被选择成熟,这一过程称为阳性选择。T细胞抗原受体(TCR)对I类或II类MHC的特异性影响其向CD4或CD8谱系的分化。这可能通过定向机制发生,也可能通过随机分化,随后是一个选择步骤,该步骤只允许CD8+、I类特异性和CD4+、II类特异性细胞存活。我们构建了一个在T细胞特异性CD2调控序列控制下表达CD8转基因的小鼠品系。虽然组成性CD8表达不影响CD4+细胞的胸腺选择,但CD8亚群中I类特异性TCR的选择得到了显著改善。这一结果与阳性选择模型一致,即在同时表达CD4和CD8的发育阶段发生选择,I类MHC的阳性选择产生一个指导性信号,引导细胞分化为CD8谱系。