Tan Joanne B, Visan Ioana, Yuan Julie S, Guidos Cynthia J
Program in Developmental Biology, Hospital for Sick Children Research Institute, Toronto, Ontario M5G 1X8, Canada.
Nat Immunol. 2005 Jul;6(7):671-9. doi: 10.1038/ni1217. Epub 2005 Jun 12.
Signaling through the transmembrane Notch1 receptor directs thymus-seeding progenitors (TSPs) to suppress their B cell potential and 'choose' the T cell fate. Present paradigms suggest that TSPs are contained in the multipotent early T lineage precursor (ETP) subset of thymocytes. However, we show here that the B cell potential of ETPs was not augmented in microenvironments that limited Notch1 activation. Furthermore, low-threshold Notch1 signals suppressed B cell production by TSPs before they reached the ETP stage. Notch1 signals of a higher threshold were needed to drive proliferation of ETPs and development into CD4(+)CD8(+) double-positive thymocytes. Thus, TSPs can be differentiated from all previously identified early T cell progenitors by their robust B cell potential and exquisite sensitivity to Notch1 signals.
通过跨膜Notch1受体发出的信号引导胸腺播种祖细胞(TSP)抑制其B细胞潜能并“选择”T细胞命运。目前的范例表明,TSP包含在胸腺细胞的多能早期T谱系前体(ETP)亚群中。然而,我们在此表明,在限制Notch1激活的微环境中,ETP的B细胞潜能并未增强。此外,低阈值Notch1信号在TSP到达ETP阶段之前就抑制了它们的B细胞产生。需要更高阈值的Notch1信号来驱动ETP的增殖并发育成CD4(+)CD8(+)双阳性胸腺细胞。因此,TSP可以通过其强大的B细胞潜能和对Notch1信号的高度敏感性与所有先前鉴定的早期T细胞祖细胞区分开来。