コンテンツへスキップ
Merck

Notch signaling represses p63 expression in the developing surface ectoderm.

Development (Cambridge, England) (2013-08-09)
Ana Mafalda Baptista Tadeu, Valerie Horsley
要旨

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.

材料
製品番号
ブランド
製品内容

Sigma-Aldrich
モノクロナール抗β-アクチン マウス宿主抗体, clone AC-15, ascites fluid
Sigma-Aldrich
Anti-Cytokeratin 18 Antibody, clone RGE53, clone RGE53, Chemicon®, from mouse
Sigma-Aldrich
抗NOTCH4抗体 ウサギ宿主抗体, ~1 mg/mL, affinity isolated antibody, buffered aqueous solution