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当缺乏CD4时,MHC II类特异性T细胞可在CD8谱系中发育。

MHC class II-specific T cells can develop in the CD8 lineage when CD4 is absent.

作者信息

Matechak E O, Killeen N, Hedrick S M, Fowlkes B J

机构信息

Laboratory of Cellular and Molecular Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892-0420, USA.

出版信息

Immunity. 1996 Apr;4(4):337-47. doi: 10.1016/s1074-7613(00)80247-2.

Abstract

The generation of mature CD4 T cells from CD4+CD8+ precursor thymocytes usually requires corecognition of class II MHC by a TCR and CD4, while the production of mature CD8 T cells requires corecognition of class I MHC by a TCR and CD8. To assess the role of the CD4 coreceptor in development and lineage commitment, we generated CD4-deficient mice expressing a transgenic class II-specific TCR. Surprisingly, in the absence of CD4 a large number of T cells mature, but these cells appear in the CD8 lineage. Thus, when CD4 is present, the majority of immature T cells with this class II-specific TCR choose the CD4 lineage but develop in the CD8 pathway when CD4 is absent. The results indicate that even for TCRs that are not dependent on coreceptor for MHC recognition, the coreceptor can influence the lineage choice. These findings are considered in terms of a quantitative signaling model for CD4/CD8 lineage commitment.

摘要

从CD4⁺CD8⁺前体胸腺细胞生成成熟的CD4 T细胞通常需要TCR和CD4对II类MHC进行共识别,而成熟CD8 T细胞的产生则需要TCR和CD8对I类MHC进行共识别。为了评估CD4共受体在发育和谱系定向中的作用,我们构建了表达转基因II类特异性TCR的CD4缺陷小鼠。令人惊讶的是,在没有CD4的情况下,大量T细胞成熟,但这些细胞出现在CD8谱系中。因此,当存在CD4时,大多数带有这种II类特异性TCR的未成熟T细胞选择CD4谱系,但在没有CD4时则沿CD8途径发育。结果表明,即使对于不依赖共受体进行MHC识别的TCR,共受体也能影响谱系选择。根据CD4/CD8谱系定向的定量信号模型对这些发现进行了考量。

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