Unité d'Immunité Innée, Institut Pasteur, INSERM U668, Paris, France.
J Immunol. 2010 Nov 1;185(9):4993-7. doi: 10.4049/jimmunol.1002273. Epub 2010 Oct 1.
Although NK cells in the mouse are thought to develop in the bone marrow, a small population of NK cells in the thymus has been shown to derive from a GATA3-dependent pathway. Characteristically, thymic NK cells express CD127 and few Ly49 molecules and lack CD11b. Because these NK cells develop in the thymus, the question of their relationship to the T cell lineage has been raised. Using several different mouse models, we find that unlike T cells, thymic NK cells are not the progeny of Rorc-expressing progenitors and do not express Rag2 or rearrange the TCRγ locus. We further demonstrate that thymic NK cells develop independently of the Notch signaling pathway, supporting the idea that thymic NK cells represent bona fide NK cells that can develop independently of all T cell precursors.
尽管人们认为小鼠中的 NK 细胞是在骨髓中发育的,但已有研究表明,胸腺中存在一小部分 NK 细胞来源于 GATA3 依赖性途径。典型的是,胸腺 NK 细胞表达 CD127 和少数 Ly49 分子,并且缺乏 CD11b。由于这些 NK 细胞在胸腺中发育,因此它们与 T 细胞谱系的关系引起了人们的关注。使用几种不同的小鼠模型,我们发现与 T 细胞不同,胸腺 NK 细胞不是表达 Rorc 的祖细胞的后代,也不表达 Rag2 或重排 TCRγ 基因座。我们进一步证明,胸腺 NK 细胞的发育独立于 Notch 信号通路,这支持了胸腺 NK 细胞代表真正的 NK 细胞的观点,它们可以独立于所有 T 细胞前体发育。