Anderson G, Pongracz J, Parnell S, Jenkinson E J
Department of Anatomy, MRC Centre for Immune Regulation, Division of Immunity and Infection, Medical School, University of Birmingham, Edgbaston, Birmingham, GB.
Eur J Immunol. 2001 Nov;31(11):3349-54. doi: 10.1002/1521-4141(200111)31:11<3349::aid-immu3349>3.0.co;2-s.
Thymic epithelial cells are specialized to play essential roles at multiple stages of T cell development in the thymus, yet the molecular basis of this specialization is largely unknown. Recently, the Notch family of transmembrane proteins has been implicated in thymocyte development. Such proteins interact with cell surface proteins of the Delta-like and Jagged families. It is known that Notch ligands are expressed intrathymically, and that Notch signaling is regulated by Notch ligands expressed on either the same or third-party cells. However, functional analysis of Notch ligand expression, and elucidation of the mechanism of Notch ligand signaling in thymocyte development, are unclear. Here, we find that Notch ligand expression in the thymus is compartmentalized, with MHC class II(+) thymic epithelium, but not thymocytes nor dendritic cells, expressing Jagged-1, Jagged-2 and Delta-like-1. We also provide evidence that contact with Notch ligands on thymic epithelium is necessary to activate and sustain Notch signaling in thymocytes, and that this can occur independently of positive selection induction. Our data suggest that Notch ligand expression by thymic epithelium may partly explain the specialization of these cells in supporting thymocyte development, by regulating Notch activation via an inductive signaling mechanism independently of signaling leading to positive selection.
胸腺上皮细胞在胸腺中T细胞发育的多个阶段发挥着重要作用,然而这种特化的分子基础在很大程度上尚不清楚。最近,跨膜蛋白Notch家族与胸腺细胞发育有关。这类蛋白与Delta样和锯齿状家族的细胞表面蛋白相互作用。已知Notch配体在胸腺内表达,且Notch信号由在同一细胞或第三方细胞上表达的Notch配体调节。然而,Notch配体表达的功能分析以及Notch配体信号在胸腺细胞发育中的机制尚不清楚。在此,我们发现胸腺中Notch配体的表达是分区的,主要组织相容性复合体II类(MHC II)阳性的胸腺上皮表达锯齿状蛋白-1、锯齿状蛋白-2和Delta样蛋白-1,而胸腺细胞和树突状细胞不表达。我们还提供证据表明,与胸腺上皮上的Notch配体接触对于激活和维持胸腺细胞中的Notch信号是必要的,并且这可以独立于阳性选择诱导而发生。我们的数据表明,胸腺上皮表达Notch配体可能部分解释了这些细胞在支持胸腺细胞发育方面的特化,即通过一种诱导信号机制调节Notch激活,而该机制独立于导致阳性选择的信号。