Urban Julie A, Brugmann William, Winandy Susan
Department of Microbiology-Immunology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.
J Immunol. 2009 Apr 1;182(7):3955-9. doi: 10.4049/jimmunol.0802869.
Positive selection is a critical T cell developmental checkpoint that is driven by TCR signals. Enhanced positive selection toward the CD4 lineage occurs in the absence of Ikaros. One explanation for this phenotype is that Ikaros establishes the TCR signaling threshold that must be overcome for positive selection to occur. In the current study, this possibility is explored through the use of CD3zeta ITAM transgenic mice that express a CD3 zeta-chain with zero, one, or three ITAMs and an MHC class II (DO11.10)- or MHC class I (H-Y)-restricted TCR transgene. Using this system, we demonstrate that in the absence of Ikaros, thymocytes are able to mature into the CD4 lineage with reduced TCR signaling potential compared with that required to drive the maturation of wild-type thymocytes. We also demonstrate that maturation into the CD8 lineage is enhanced under conditions of reduced TCR signaling potential in the absence of Ikaros.
阳性选择是由TCR信号驱动的关键T细胞发育检查点。在缺乏Ikaros的情况下,向CD4谱系的阳性选择增强。对此表型的一种解释是,Ikaros确立了阳性选择发生所必须克服的TCR信号阈值。在本研究中,通过使用表达具有零个、一个或三个免疫受体酪氨酸活化基序(ITAM)的CD3ζ链以及II类主要组织相容性复合体(DO11.10)或I类主要组织相容性复合体(H-Y)限制性TCR转基因的CD3ζ ITAM转基因小鼠来探究这种可能性。利用该系统,我们证明在缺乏Ikaros的情况下,与驱动野生型胸腺细胞成熟所需的信号潜力相比,胸腺细胞能够以降低的TCR信号潜力成熟为CD4谱系。我们还证明,在缺乏Ikaros的情况下,在TCR信号潜力降低的条件下,向CD8谱系的成熟增强。