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Merck
CN
  • Notch signaling represses p63 expression in the developing surface ectoderm.

Notch signaling represses p63 expression in the developing surface ectoderm.

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

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.

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Sigma-Aldrich
单克隆抗 β-肌动蛋白抗体 小鼠抗, clone AC-15, ascites fluid
Sigma-Aldrich
抗细胞角蛋白18抗体,克隆GE53, clone RGE53, Chemicon®, from mouse
Sigma-Aldrich
Anti-NOTCH4 antibody produced in rabbit, ~1 mg/mL, affinity isolated antibody, buffered aqueous solution