
pmid: 9804358
Epidermal differentiation, as keratinocytes go through different layers to the skin surface, may imply a differential activation of Notch transmembrane proteins. In mouse, as recently shown in Drosophila, Notch activation by its ligands may be modulated by Fringe secreted proteins. Therefore, we cloned the mouse homolog of Radical-fng, synthesized riboprobes for Lunatic-fng, Manic-fng, and Radical-fng, and examined their expression during epidermal differentiation. Expression of all three genes is differentially activated during embryonic epidermal stratification. Manic-fng and Lunatic-fng are expressed in the basal layer, whereas Lunatic-fng is expressed in the granular layer and Radical-fng is restricted to the most differentiated nucleated layer. This expression decreases by a few days postnatally and can be reactivated by retinoic acid treatment, which triggers a new distribution of Fringe transcripts and a thickening of the granular layer. Therefore, Manic, Lunatic, and Radical Fringe by modulating the Notch pathway may play a key role in defining the different steps of keratinocyte differentiation.
Keratinocytes, skin, Transcription, Genetic, Notch pathway, Gene Expression, Tretinoin, Dermatology, Biochemistry, Mice, retinoic acid, Animals, RNA, Messenger, Molecular Biology, In Situ Hybridization, Skin, cell interactions, Glycosyltransferases, Proteins, Cell Differentiation, Cell Biology, Glucosyltransferases, Intercellular Signaling Peptides and Proteins, Epidermis
Keratinocytes, skin, Transcription, Genetic, Notch pathway, Gene Expression, Tretinoin, Dermatology, Biochemistry, Mice, retinoic acid, Animals, RNA, Messenger, Molecular Biology, In Situ Hybridization, Skin, cell interactions, Glycosyltransferases, Proteins, Cell Differentiation, Cell Biology, Glucosyltransferases, Intercellular Signaling Peptides and Proteins, Epidermis
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