Abstract
Using the epidermis-specific cytokeratin 14 promoter to deliver HGF exclusively from epidermal keratinocytes, we have examined the potential of hepatocyte growth factor (HGF) secreted from the normal environment to control morphogenesis. The transgenic mice displayed a significant increase of the number of melanocytes and their precursors in embryos starting not later than 16.5 dpc, and then after birth an explosive increase of dermal melanocytes started within 1 week, and these melanocytes were maintained throughout the entire life of the mice. Thus, HGF acts as a paracrine agent to promote survival, proliferation and differentiation of melanocyte precursors in vivo, and eventually causes melanocytosis. Loss of E-cadherin expression in dermal melanocyte precursors suggests that HGF caused dermal localization of melanocytes and their precursors by down-regulation of E-cadherin molecules.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Animals, Newborn
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Cadherins / genetics
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Cadherins / metabolism
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Ear, External
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Gene Expression Regulation, Developmental
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Hepatocyte Growth Factor / genetics*
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Hepatocyte Growth Factor / metabolism
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Intramolecular Oxidoreductases / metabolism
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Keratinocytes / physiology*
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Keratins / genetics
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Melanocytes / pathology
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Melanocytes / physiology*
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Mice
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Mice, Transgenic
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Promoter Regions, Genetic
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Proto-Oncogene Proteins c-kit / metabolism
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Proto-Oncogene Proteins c-met / metabolism
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Skin / embryology
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Skin / growth & development
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Skin / pathology
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Skin Diseases / genetics*
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Skin Diseases / pathology
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Skin Pigmentation / genetics
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Stem Cell Factor / metabolism
Substances
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Cadherins
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Stem Cell Factor
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Hepatocyte Growth Factor
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Keratins
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Proto-Oncogene Proteins c-kit
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Proto-Oncogene Proteins c-met
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Intramolecular Oxidoreductases
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dopachrome isomerase