Centre for Cytometry and Fluorescence Microscopy UCM, Complutense University of Madrid, 28040, Madrid, Spain.
Department of Cell Biology, Faculty of Biology, Complutense University of Madrid, 28040, Madrid, Spain.
Histochem Cell Biol. 2019 Dec;152(6):397-413. doi: 10.1007/s00418-019-01818-z. Epub 2019 Sep 24.
The mechanisms that determine the commitment of thymic epithelial precursors to the two major thymic epithelial cell lineages, cTECs and mTECs, remain unknown. Here we show that FoxN1 nu mutation, which abolishes thymic epithelium differentiation, results in the formation of a tubular branched structure according to a typical branching morphogenesis and tubulogenesis developmental pattern. In the presence of FoxN1, in alymphoid NSG and fetal Ikaros-/- thymi, there is no lumen formation and only partial apical differentiation. This initiates cortex-medulla differentiation inducing expression of medullary genes in the apically differentiating cells and of cortical genes in the non-apically differentiating cells, which will definitely differentiate in wt and postnatal Ikaros-/- mice. Therefore, the thymus development is based on a branching morphogenesis and tubulogenesis developmental pattern: FoxN1 expression in the thymic primordium inhibits tubulogenesis and induces the expression of genes involved in TEC differentiation, which culminates with the expression of functional cell markers, i.e., MHCII, CD80, Aire in both postnatal Ikaros-/- and WT thymi after arrival of lymphoid progenitor cells.
目前尚不清楚决定胸腺上皮前体细胞向两个主要的胸腺上皮细胞谱系(cTECs 和 mTECs)分化的机制。本文中,我们发现 FoxN1nu 突变(可消除胸腺上皮细胞分化)会导致形成管状分支结构,这符合典型的分支形态发生和管状发生发育模式。在 FoxN1 存在的情况下,在无淋巴 NSG 和 Ikaros-/- 胎儿胸腺中,不会形成腔且只有部分顶部分化。这会启动皮质-髓质分化,在顶部分化的细胞中诱导髓质基因的表达,在非顶部分化的细胞中诱导皮质基因的表达,这些细胞在 wt 和产后 Ikaros-/- 小鼠中肯定会分化。因此,胸腺发育基于分支形态发生和管状发生发育模式:FoxN1 在胸腺原基中的表达抑制管状发生并诱导参与 TEC 分化的基因表达,最终表达功能性细胞标记物,即在淋巴细胞祖细胞到达后,产后 Ikaros-/- 和 WT 胸腺中的 MHCII、CD80 和 Aire。