Ciofani Maria, Knowles Gisèle C, Wiest David L, von Boehmer Harald, Zúñiga-Pflücker Juan Carlos
Department of Immunology, University of Toronto, Sunnybrook Research Institute, 2075 Bayview Avenue, Toronto, Ontario M4N 3M5, Canada.
Immunity. 2006 Jul;25(1):105-16. doi: 10.1016/j.immuni.2006.05.010. Epub 2006 Jun 29.
Signals transduced by Notch receptors are indispensable for T cell specification and differentiation of alphabeta T lineage cells. However, the role of Notch signals during alphabeta versus gammadelta T lineage decision remains controversial. Here, we addressed this question by employing a clonal analysis of CD4(-)CD8(-) (DN) progenitor potential to position the divergence of alphabeta and gammadelta T cell lineages to the late DN2 to DN3 developmental stages. Accordingly, alphabeta and gammadelta precursor frequencies within these T cell progenitor subsets were determined, both in the presence and absence of Notch signaling through Delta-like 1. Notch signals were found to be critical for the DN to CD4(+)CD8(+) (DP) transition, irrespective of the identity (pTalphabeta or gammadelta) of the inducing T cell receptor complex, whereas gammadelta T cells developed from gammadeltaTCR-expressing T cell progenitors in the absence of further Notch ligand interaction. Collectively, our findings demonstrate a differential, stage-specific requirement for Notch receptor-ligand interactions in the differentiation of alphabeta and gammadelta T cells from T cell progenitors.
Notch受体转导的信号对于αβ T谱系细胞的T细胞特化和分化是不可或缺的。然而,Notch信号在αβ与γδ T谱系决定过程中的作用仍存在争议。在此,我们通过对CD4(-)CD8(-)(双阴性,DN)祖细胞潜能进行克隆分析,将αβ和γδ T细胞谱系的分化定位到DN2晚期至DN3发育阶段,从而解决了这个问题。相应地,我们测定了在存在和不存在通过Delta样1的Notch信号的情况下,这些T细胞祖细胞亚群内αβ和γδ前体频率。结果发现,Notch信号对于从DN向CD4(+)CD8(+)(双阳性,DP)转变至关重要,而与诱导性T细胞受体复合物的身份(pTαβ或γδ)无关,而γδ T细胞是在没有进一步Notch配体相互作用的情况下,从表达γδTCR的T细胞祖细胞发育而来。总的来说,我们的研究结果表明,在T细胞祖细胞向αβ和γδ T细胞分化过程中,Notch受体 - 配体相互作用存在差异的、阶段特异性的需求。