Kimura Motoko Y, Thomas Julien, Tai Xuguang, Guinter Terry I, Shinzawa Miho, Etzensperger Ruth, Li Zhenhu, Love Paul, Nakayama Toshinori, Singer Alfred
Experimental Immunology Branch, National Cancer Institute, US National Institutes of Health, Bethesda, Maryland, USA.
Laboratory of Mammalian Genes and Development, Eunice Kennedy Schriver National Institute of Child Health and Human Development, US National Institutes of Health, Bethesda, Maryland, USA.
Nat Immunol. 2016 Dec;17(12):1415-1423. doi: 10.1038/ni.3560. Epub 2016 Sep 26.
Major histocompatibility complex class I (MHC I) positive selection of CD8 T cells in the thymus requires that T cell antigen receptor (TCR) signaling end in time for cytokines to induce Runx3d, the CD8-lineage transcription factor. We examined the time required for these events and found that the overall duration of positive selection was similar for all CD8 thymocytes in mice, despite markedly different TCR signaling times. Notably, prolonged TCR signaling times were counter-balanced by accelerated Runx3d induction by cytokines and accelerated differentiation into CD8 T cells. Consequently, lineage errors did not occur except when MHC I-TCR signaling was so prolonged that the CD4-lineage-specifying transcription factor ThPOK was expressed, preventing Runx3d induction. Thus, our results identify a compensatory signaling mechanism that prevents lineage-fate errors by dynamically modulating Runx3d induction rates during MHC I positive selection.
胸腺中CD8 T细胞的主要组织相容性复合体I类(MHC I)阳性选择要求T细胞抗原受体(TCR)信号及时终止,以便细胞因子诱导CD8谱系转录因子Runx3d。我们研究了这些事件所需的时间,发现尽管TCR信号传导时间明显不同,但小鼠中所有CD8胸腺细胞阳性选择的总持续时间相似。值得注意的是,延长的TCR信号传导时间被细胞因子加速诱导Runx3d以及加速分化为CD8 T细胞所抵消。因此,除非MHC I - TCR信号传导延长到足以表达CD4谱系特异性转录因子ThPOK并阻止Runx3d诱导,否则不会发生谱系错误。因此,我们的结果确定了一种补偿性信号机制,该机制通过在MHC I阳性选择过程中动态调节Runx3d诱导率来防止谱系命运错误。