Liu Cunlan, Saito Fumi, Liu Zhijie, Lei Yu, Uehara Shoji, Love Paul, Lipp Martin, Kondo Shunzo, Manley Nancy, Takahama Yousuke
Division of Experimental Immunology, Institute for Genome Research, University of Tokushima, Tokushima 770-8503, Japan.
Blood. 2006 Oct 15;108(8):2531-9. doi: 10.1182/blood-2006-05-024190. Epub 2006 Jun 29.
Thymus seeding by T-lymphoid progenitor cells is a prerequisite for T-cell development. However, molecules guiding thymus colonization and their roles before and after thymus vascularization are unclear. Here we show that mice doubly deficient for chemokine receptors CCR7 and CCR9 were defective specifically in fetal thymus colonization before, but not after, thymus vascularization. The defective prevascular fetal thymus colonization was followed by selective loss of the first wave of T-cell development generating epidermal Vgamma3(+) gammadelta T cells. Unexpectedly, CCL21, a CCR7 ligand, was expressed not by Foxn1-dependent thymic primordium but by Gcm2-dependent parathyroid primordium, whereas CCL25, a CCR9 ligand, was predominantly expressed by Foxn1-dependent thymic primordium, revealing the role of the adjacent parathyroid in guiding fetal thymus colonization. These results indicate coordination between Gcm2-dependent parathyroid and Foxn1-dependent thymic primordia in establishing CCL21/CCR7- and CCL25/CCR9-mediated chemokine guidance essential for prevascular fetal thymus colonization.
T淋巴细胞祖细胞在胸腺中定植是T细胞发育的前提条件。然而,引导胸腺定植的分子及其在胸腺血管化前后的作用尚不清楚。在此,我们发现趋化因子受体CCR7和CCR9双缺陷的小鼠,在胸腺血管化之前的胎儿胸腺定植过程中存在特异性缺陷,但在胸腺血管化之后则无此缺陷。血管化前胎儿胸腺定植缺陷之后,会选择性地丧失产生表皮Vγ3(+) γδ T细胞的第一波T细胞发育。出乎意料的是,CCR7配体CCL21并非由Foxn1依赖性胸腺原基表达,而是由Gcm2依赖性甲状旁腺原基表达,而CCR9配体CCL25主要由Foxn1依赖性胸腺原基表达,这揭示了相邻甲状旁腺在引导胎儿胸腺定植中的作用。这些结果表明,在建立对血管化前胎儿胸腺定植至关重要的CCL21/CCR7和CCL25/CCR9介导的趋化因子引导过程中,Gcm2依赖性甲状旁腺原基和Foxn1依赖性胸腺原基之间存在协调作用。