Mayer Carlos E, Žuklys Saulius, Zhanybekova Saule, Ohigashi Izumi, Teh Hong-Ying, Sansom Stephen N, Shikama-Dorn Noriko, Hafen Katrin, Macaulay Iain C, Deadman Mary E, Ponting Chris P, Takahama Yousuke, Holländer Georg A
Department of Biomedicine, University of Basel, Basel, Switzerland.
Division of Experimental Immunology, Institute for Genome Research, University of Tokushima, Japan.
Eur J Immunol. 2016 Apr;46(4):846-56. doi: 10.1002/eji.201545995. Epub 2016 Jan 18.
Intrathymic T-cell development is critically dependent on cortical and medullary thymic epithelial cells (TECs). Both epithelial subsets originate during early thymus organogenesis from progenitor cells that express the thymoproteasome subunit β5t, a typical feature of cortical TECs. Using in vivo lineage fate mapping, we demonstrate in mice that β5t(+) TEC progenitors give rise to the medullary TEC compartment early in life but significantly limit their contribution once the medulla has completely formed. Lineage-tracing studies at single cell resolution demonstrate for young mice that the postnatal medulla is expanded from individual β5t(+) cortical progenitors located at the cortico-medullary junction. These results therefore not only define a developmental window during which the expansion of medulla is efficiently enabled by progenitors resident in the thymic cortex, but also reveal the spatio-temporal dynamics that control the growth of the thymic medulla.
胸腺内T细胞的发育严重依赖于皮质和髓质胸腺上皮细胞(TECs)。这两种上皮亚群在胸腺早期器官发生过程中起源于表达胸腺蛋白酶体亚基β5t的祖细胞,这是皮质TECs的一个典型特征。通过体内谱系命运图谱,我们在小鼠中证明,β5t(+) TEC祖细胞在生命早期产生髓质TEC区室,但一旦髓质完全形成,它们的贡献就会显著受限。单细胞分辨率的谱系追踪研究表明,对于幼鼠来说,出生后的髓质是由位于皮质-髓质交界处的单个β5t(+) 皮质祖细胞扩展而来的。因此,这些结果不仅定义了一个发育窗口,在此期间胸腺皮质中的祖细胞有效地促进了髓质的扩展,而且还揭示了控制胸腺髓质生长的时空动态。