Chan S, Waltzinger C, Tarakhovsky A, Benoist C, Mathis D
Institut de Génétique et de Biologie Moléculaire et Cellulaire (CNRS/INSERM/ULP) Illkirch, C.U. de Strasbourg, France.
Eur J Immunol. 1999 Sep;29(9):2916-22. doi: 10.1002/(SICI)1521-4141(199909)29:09<2916::AID-IMMU2916>3.0.CO;2-I.
Combining CD5-null, MHC-deficient and lineage-specific reporter animals, we have investigated the influence of CD5 on positive selection and the choice of CD4- versus CD8-lineage commitment on broad populations of thymocytes. CD5 has no obvious quantitative effect in wild-type mice. In mice lacking MHC class II molecules, however, increased numbers of transitional, class I-selected CD4+ CD8(int) CD3(hi) cells were positively selected in the absence of CD5. Importantly, they were committed to the CD4 lineage. Our results indicate that CD5 negatively regulates the differentiation of CD4-committed cells in suboptimal conditions, thus perhaps serving to tighten the correlation between restriction of the TCR and lineage choice.
通过将 CD5 基因缺失、MHC 缺陷和谱系特异性报告基因动物相结合,我们研究了 CD5 对广泛胸腺细胞群体阳性选择以及 CD4 与 CD8 谱系分化选择的影响。在野生型小鼠中,CD5 没有明显的定量效应。然而,在缺乏 MHC II 类分子的小鼠中,在没有 CD5 的情况下,有更多数量的过渡型、I 类选择的 CD4+CD8(int)CD3(hi)细胞被阳性选择。重要的是,它们分化为 CD4 谱系。我们的结果表明,在次优条件下,CD5 负向调节 CD4 谱系细胞的分化,从而可能有助于加强 TCR 限制与谱系选择之间的相关性。