Department of Molecular, Cell and Developmental Biology, Yale University, 219 Prospect Street, Box 208103, New Haven, CT 06520, USA.
Development. 2013 Sep;140(18):3777-86. doi: 10.1242/dev.093948. Epub 2013 Aug 7.
The development of the mature epidermis requires a coordinated sequence of signaling events and transcriptional changes to specify surface ectodermal progenitor cells to the keratinocyte lineage. The initial events that specify epidermal keratinocytes from ectodermal progenitor cells are not well understood. Here, we use both developing mouse embryos and human embryonic stem cells (hESCs) to explore the mechanisms that direct keratinocyte fate from ectodermal progenitor cells. We show that both hESCs and murine embryos express p63 before keratin 14. Furthermore, we find that Notch signaling is activated before p63 expression in ectodermal progenitor cells. Inhibition of Notch signaling pharmacologically or genetically reveals a negative regulatory role for Notch signaling in p63 expression during ectodermal specification in hESCs or mouse embryos, respectively. Taken together, these data reveal a role for Notch signaling in the molecular control of ectodermal progenitor cell specification to the epidermal keratinocyte lineage.
成熟表皮的发育需要一系列协调的信号事件和转录变化,以将表面外胚层祖细胞特化为角蛋白细胞谱系。然而,指定表皮角质形成细胞的最初事件还不是很清楚。在这里,我们使用发育中的小鼠胚胎和人类胚胎干细胞(hESCs)来探索指导外胚层祖细胞向角质形成细胞命运的机制。我们发现 hESCs 和鼠胚胎在角蛋白 14 之前都表达 p63。此外,我们发现 Notch 信号在 hESCs 或小鼠胚胎中外胚层祖细胞中 p63 表达之前被激活。Notch 信号的药理学或遗传学抑制分别揭示了 Notch 信号在 hESCs 或小鼠胚胎中外胚层特化过程中对 p63 表达的负调控作用。总之,这些数据揭示了 Notch 信号在分子控制外胚层祖细胞特化为表皮角质形成细胞谱系中的作用。