Veltmaat Jacqueline M, Relaix Frédéric, Le Lendy T, Kratochwil Klaus, Sala Frédéric G, van Veelen Wendy, Rice Ritva, Spencer-Dene Bradley, Mailleux Arnaud A, Rice David P, Thiery Jean Paul, Bellusci Saverio
The Saban Research Institute of Childrens Hospital Los Angeles/University of Southern California, Developmental Biology Program, Los Angeles, CA 90027, USA.
Development. 2006 Jun;133(12):2325-35. doi: 10.1242/dev.02394.
Little is known about the regulation of cell fate decisions that lead to the formation of five pairs of mammary placodes in the surface ectoderm of the mouse embryo. We have previously shown that fibroblast growth factor 10 (FGF10) is required for the formation of mammary placodes 1, 2, 3 and 5. Here, we have found that Fgf10 is expressed only in the somites underlying placodes 2 and 3, in gradients across and within these somites. To test whether somitic FGF10 is required for the formation of these two placodes, we analyzed a number of mutants with different perturbations of somitic Fgf10 gradients for the presence of WNT signals and ectodermal multilayering, markers for mammary line and placode formation. The mammary line is displaced dorsally, and formation of placode 3 is impaired in Pax3ILZ/ILZ mutants, which do not form ventral somitic buds. Mammary line formation is impaired and placode 3 is absent in Gli3Xt-J/Xt-J and hypomorphic Fgf10 mutants, in which the somitic Fgf10 gradient is shortened dorsally and less overall Fgf10 is expressed, respectively. Recombinant FGF10 rescued mammogenesis in Fgf10(-/-) and Gli3Xt-J/Xt-J flanks. We correlate increasing levels of somitic FGF10 with progressive maturation of the surface ectoderm, and show that full expression of somitic Fgf10, co-regulated by GLI3, is required for the anteroposterior pattern in which the flank ectoderm acquires a mammary epithelial identity. We propose that the intra-somitic Fgf10 gradient, together with ventral elongation of the somites, determines the correct dorsoventral position of mammary epithelium along the flank.
关于导致小鼠胚胎表面外胚层形成五对乳腺基板的细胞命运决定的调控,我们所知甚少。我们之前已经表明,成纤维细胞生长因子10(FGF10)是乳腺基板1、2、3和5形成所必需的。在这里,我们发现Fgf10仅在基板2和3下方的体节中表达,在这些体节内和跨体节呈梯度分布。为了测试体节FGF10是否是这两个基板形成所必需的,我们分析了一些体节Fgf10梯度受到不同扰动的突变体,检测其是否存在WNT信号和外胚层多层化,这两种是乳腺谱系和基板形成的标志物。在不形成腹侧体节芽的Pax3ILZ/ILZ突变体中,乳腺谱系向背侧移位,基板3的形成受损。在Gli3Xt-J/Xt-J和低表达Fgf10的突变体中,乳腺谱系形成受损且基板3缺失,在这些突变体中,体节Fgf10梯度分别在背侧缩短和整体表达的Fgf10较少。重组FGF10挽救了Fgf10(-/-)和Gli3Xt-J/Xt-J侧翼的乳腺发生。我们将体节FGF10水平的升高与表面外胚层的逐渐成熟相关联,并表明由GLI3共同调控的体节Fgf10的完全表达,是侧翼外胚层获得乳腺上皮身份的前后模式所必需的。我们提出,体节内的Fgf10梯度,与体节的腹侧延伸一起,决定了乳腺上皮沿侧翼的正确背腹位置。