Wilson A, Ferrero I, MacDonald H R, Radtke F
Ludwig Institute for Cancer Research, Lausanne Branch, University of Lausanne, Epalinges, Switzerland.
J Immunol. 2000 Nov 15;165(10):5397-400. doi: 10.4049/jimmunol.165.10.5397.
Whereas most T cells arise in the thymus, a distinct lineage of extrathymically derived T cells is present in the gut mucosa. The developmental origin of extrathymic T cells is poorly understood. We show here that Notch-1, a transmembrane receptor involved in T cell fate specification of bipotential T/B precursors in the thymus, is absolutely required for the development of extrathymic (as well as thymus-derived) mature T cells in the intestinal epithelium. In the absence of Notch-1, CD117(+) T cell precursors are relatively more abundant in the gut than the thymus, whereas immature B cells accumulate in the thymus but not the gut. Collectively, these data demonstrate that Notch-1 is essential for both thymic and extrathymic T cell fate specification and further suggest that bipotential T/B precursors that do not receive a Notch-1 signal adopt a B cell fate in the thymus but become developmentally arrested in the gut.
虽然大多数T细胞在胸腺中产生,但在肠道黏膜中存在一种源自胸腺外的独特T细胞谱系。胸腺外T细胞的发育起源尚不清楚。我们在此表明,Notch-1是一种跨膜受体,参与胸腺中双潜能T/B前体细胞的T细胞命运决定,它对于肠道上皮中胸腺外(以及胸腺来源)成熟T细胞的发育是绝对必需的。在没有Notch-1的情况下,CD117(+) T细胞前体在肠道中比在胸腺中相对更为丰富,而未成熟B细胞在胸腺中积累,但不在肠道中积累。总体而言,这些数据表明Notch-1对于胸腺和胸腺外T细胞命运决定都是必不可少的,并且进一步表明未接收到Notch-1信号的双潜能T/B前体在胸腺中会采用B细胞命运,但在肠道中会发生发育停滞。