La Motte-Mohs Ross N, Herer Elaine, Zúñiga-Pflücker Juan Carlos
Department of Immunology, University of Toronto, Sunnybrook and Women's College Health Sciences Centre, Toronto, Ontario M4N 3M5, Canada.
Blood. 2005 Feb 15;105(4):1431-9. doi: 10.1182/blood-2004-04-1293. Epub 2004 Oct 19.
The Notch signaling pathway plays a key role at several stages of T-lymphocyte differentiation. However, it remained unclear whether signals induced by the Notch ligand Delta-like 1 could support full T-cell differentiation from a defined source of human hematopoietic stem cells (HSCs) in vitro. Here, we show that human cord blood-derived HSCs cultured on Delta-like 1-expressing OP9 stromal cells undergo efficient T-cell lineage commitment and sustained T-cell differentiation. A normal stage-specific program of T-cell development was observed, including the generation of CD4 and CD8 alpha beta-T-cell receptor (TCR)-bearing cells. Induction of T-cell differentiation was dependent on the expression of Delta-like 1 by the OP9 cells. Stimulation of the in vitro-differentiated T cells by TCR engagement induced the expression of T-cell activation markers and costimulatory receptors. These results establish an efficient in vitro coculture system for the generation of T cells from human HSCs, providing a new avenue for the study of early T-cell differentiation and function.
Notch信号通路在T淋巴细胞分化的多个阶段发挥关键作用。然而,Notch配体Delta样1所诱导的信号是否能够在体外支持从特定来源的人类造血干细胞(HSC)实现完全的T细胞分化,仍不清楚。在此,我们表明,在表达Delta样1的OP9基质细胞上培养的人类脐带血来源的HSC可高效地向T细胞谱系定向分化并持续进行T细胞分化。观察到了正常的T细胞发育阶段特异性程序,包括产生携带CD4和CD8αβ-T细胞受体(TCR)的细胞。T细胞分化的诱导依赖于OP9细胞表达Delta样1。通过TCR结合刺激体外分化的T细胞可诱导T细胞活化标志物和共刺激受体的表达。这些结果建立了一种从人类HSC高效生成T细胞的体外共培养系统,为早期T细胞分化和功能的研究提供了一条新途径。