Laboratory for Lymphocyte Development, RIKEN Research Center for Allergy and Immunology, Yokohama 230-0045, Japan.
Science. 2010 Jul 2;329(5987):93-6. doi: 10.1126/science.1188995.
In early T cell development, progenitors retaining the potential to generate myeloid and natural killer lineages are eventually determined to a specific T cell lineage. The molecular mechanisms that drive this determination step remain unclarified. We show that, when murine hematopoietic progenitors were cultured on immobilized Notch ligand DLL4 protein in the presence of a cocktail of cytokines including interleukin-7, progenitors developing toward T cells were arrested and the arrested cells entered a self-renewal cycle, maintaining non-T lineage potentials. Reduced concentrations of interleukin-7 promoted T cell lineage determination. A similar arrest and self-renewal of progenitors were observed in thymocytes of mice deficient in the transcription factor Bcl11b. Our study thus identifies the earliest checkpoint during T cell development and shows that it is Bcl11b-dependent.
在 T 细胞早期发育过程中,具有生成髓系和自然杀伤谱系潜力的祖细胞最终被决定为特定的 T 细胞谱系。驱动这一决定步骤的分子机制仍不清楚。我们表明,当在包含白细胞介素 7 等细胞因子的混合物的情况下,将小鼠造血祖细胞培养在固定化的 Notch 配体 DLL4 蛋白上时,朝向 T 细胞发育的祖细胞被阻滞,并且被阻滞的细胞进入自我更新周期,维持非 T 谱系潜能。白细胞介素 7 的浓度降低促进了 T 细胞谱系的决定。在转录因子 Bcl11b 缺失的小鼠的胸腺细胞中也观察到类似的祖细胞阻滞和自我更新。因此,我们的研究确定了 T 细胞发育过程中的最早检查点,并表明它依赖于 Bcl11b。