Huang Eugene Y, Gallegos Alena M, Richards Sabrina M, Lehar Sophie M, Bevan Michael J
Department of Immunology, Howard Hughes Medical Institute, University of Washington, Seattle, WA 98195, USA.
J Immunol. 2003 Sep 1;171(5):2296-304. doi: 10.4049/jimmunol.171.5.2296.
Notch1 plays a critical role in regulating T lineage commitment during the differentiation of lymphoid precursors. The physiological relevance of Notch1 signaling during subsequent stages of T cell differentiation has been more controversial. This is due in part to conflicting data from studies examining the overexpression or targeted deletion of Notch1 and to difficulties in distinguishing between the activities of multiple Notch family members and their ligands, which are expressed in the thymus. We employed a polyclonal antiserum against the extracellular domain of Notch1 to study surface expression during thymopoiesis. We found high levels of Notch1 on the cell surface only on double negative (DN) stage 2 through the immature single-positive stage of thymocyte development, before the double-positive (DP) stage. The Notch signaling pathway, as read out by Deltex1 expression levels, is highly active in DN thymocytes. When an active Notch1 transgene, Notch1IC, is exogenously introduced into thymocytes of recombinase-activating gene 2-deficient mice, it promotes proliferation and development to the DP stage following anti-CD3 treatment without apparently affecting the intensity of pre-TCR signaling. In addition, a stromal cell line expressing the Notch ligand, Delta-like-1, promotes the in vitro expansion of wild-type DN3 thymocytes in vitro. Consistent with other recent reports, these data suggest a role for Notch1 during the DN to DP stage of thymocyte maturation and suggest a cellular mechanism by which Notch1IC oncogenes could contribute to thymoma development and maintenance.
Notch1在淋巴细胞前体分化过程中调节T细胞谱系定向中发挥关键作用。Notch1信号在T细胞分化后续阶段的生理相关性更具争议性。部分原因是研究Notch1过表达或靶向缺失的数据相互矛盾,以及难以区分胸腺中表达的多个Notch家族成员及其配体的活性。我们使用针对Notch1细胞外结构域的多克隆抗血清来研究胸腺生成过程中的表面表达。我们发现,在双阳性(DP)阶段之前,仅在胸腺细胞发育的双阴性(DN)2期至未成熟单阳性阶段,细胞表面存在高水平的Notch1。以Deltex1表达水平衡量的Notch信号通路在DN胸腺细胞中高度活跃。当将活性Notch1转基因Notch1IC外源导入重组酶激活基因2缺陷小鼠的胸腺细胞时,经抗CD3处理后,它可促进细胞增殖并发育至DP阶段,且显然不影响前TCR信号的强度。此外,表达Notch配体Delta-like-1的基质细胞系可促进野生型DN3胸腺细胞的体外扩增。与其他近期报道一致,这些数据表明Notch1在胸腺细胞成熟的DN至DP阶段发挥作用,并提示了Notch1IC癌基因可能促进胸腺瘤发生和维持的细胞机制。