Benveniste P, Takahama Y, Wiest D L, Nakayama T, Sharrow S O, Singer A
Experimental Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
Proc Natl Acad Sci U S A. 1994 Jul 19;91(15):6933-7. doi: 10.1073/pnas.91.15.6933.
Immature precursor cells are induced in the thymus to express clonotypic T-cell antigen receptors (TCRs) and to differentiate into mature T cells. Perhaps the least understood event which occurs during intrathymic development is the positive selection of immature CD4+CD8+ thymocytes for differentiation into mature CD4+ and CD8+ T cells based on the TCR specificity individual thymocytes express. TCR expression by CD4+CD8+ thymocytes is quantitatively regulated by CD4-mediated activation of p56lck protein-tyrosine kinase whose activity can in turn be regulated by the membrane-bound protein-tyrosine-phosphatase CD45. Here we show that antibody engagement of CD45 external domains enhances Lck tyrosine kinase activity in CD4+CD8+ thymocytes, inhibits TCR expression, and inhibits differentiation of immature CD4+CD8+ thymocytes into mature T cells. Thus, engagement of the external domains of CD45 tyrosine phosphatase can regulate the ability of immature CD4+CD8+ thymocytes to undergo positive selection, suggesting an important regulatory role for intrathymic ligands that are capable of engaging CD45 within the thymus.
未成熟的前体细胞在胸腺中被诱导表达克隆型T细胞抗原受体(TCR)并分化为成熟的T细胞。在胸腺内发育过程中发生的最不清楚的事件可能是,基于单个胸腺细胞所表达的TCR特异性,对未成熟的CD4+CD8+胸腺细胞进行阳性选择,使其分化为成熟的CD4+和CD8+T细胞。CD4+CD8+胸腺细胞的TCR表达受到CD4介导的p56lck蛋白酪氨酸激酶激活的定量调节,而该激酶的活性又可由膜结合蛋白酪氨酸磷酸酶CD45调节。在此我们表明,CD45胞外结构域的抗体结合增强了CD4+CD8+胸腺细胞中Lck酪氨酸激酶的活性,抑制了TCR表达,并抑制了未成熟的CD4+CD8+胸腺细胞分化为成熟T细胞。因此,CD45酪氨酸磷酸酶胞外结构域的结合可调节未成熟的CD4+CD8+胸腺细胞进行阳性选择的能力,这表明胸腺内能够结合CD45的配体具有重要的调节作用。