Title : A novel DLX3-PKC integrated signaling network drives keratinocyte differentiation.

Pub. Date : 2017 Apr

PMID : 28186503






3 Functional Relationships(s)
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1 We found that following 12-O-tetradecanoyl-phorbol-13-acetate (TPA) topical treatment, DLX3 expression is significantly upregulated in the epidermis and keratinocytes from mice overexpressing PKCalpha by transgenic targeting (K5-PKCalpha), resulting in cell cycle block and terminal differentiation. Tetradecanoylphorbol Acetate distal-less homeobox 3 Mus musculus
2 We found that following 12-O-tetradecanoyl-phorbol-13-acetate (TPA) topical treatment, DLX3 expression is significantly upregulated in the epidermis and keratinocytes from mice overexpressing PKCalpha by transgenic targeting (K5-PKCalpha), resulting in cell cycle block and terminal differentiation. Tetradecanoylphorbol Acetate distal-less homeobox 3 Mus musculus
3 Of particular significance, transcriptional activation of epidermal barrier, antimicrobial peptide and cytokine genes is significantly increased in DLX3cKO skin and further increased by TPA-dependent PKC activation. Tetradecanoylphorbol Acetate distal-less homeobox 3 Mus musculus