Literature DB >> 12213097

Keratinocytes control the proliferation and differentiation of cultured epidermal melanocytes from ultraviolet radiation B-induced pigmented spots in the dorsal skin of hairless mice.

Tomohisa Hirobe1, Rikako Furuya, Satoru Akiu, Ohji Ifuku, Minoru Fukuda.   

Abstract

Long-term exposure of ultraviolet radiation B (UVB)-induced pigmented spots in the dorsal skin of hairless mice of Hos:(HR-1 X HR//De) F1. Previous study showed that the proliferative and differentiative activities of cultured epidermal melanoblasts/melanocytes from UVB-induced pigmented spots increased with the development of the pigmented spots. To determine whether the increase in the proliferative and differentiative activities of epidermal melanoblasts/melanocytes was brought about by direct changes in melanocytes, or by indirect changes in surrounding keratinocytes, pure cultured melanoblasts/melanocytes and keratinocytes were prepared and co-cultured in combination with control and irradiated mice in a serum-free culture medium. Keratinocytes from irradiated mice stimulated the proliferation and differentiation of both neonatal and adult non-irradiated melanoblasts/melanocytes more greatly than those from non-irradiated mice. In contrast, both non-irradiated and irradiated adult melanocytes proliferated and differentiated similarly when they were co-cultured with irradiated adult keratinocytes. These results suggest that the increased proliferative and differentiative activities of mouse epidermal melanocytes from UVB-induced pigmented spots are regulated by keratinocytes, rather than melanocytes.

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Year:  2002        PMID: 12213097     DOI: 10.1034/j.1600-0749.2002.02052.x

Source DB:  PubMed          Journal:  Pigment Cell Res        ISSN: 0893-5785


  6 in total

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5.  Association between melanocytic neoplasms and seborrheic keratosis: more than a coincidental collision?

Authors:  Jennifer Defazio; Iris Zalaudek; Klaus J Busam; Carlo Cota; Ashfaq Marghoob
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6.  Alleviation of Ultraviolet-B Radiation-Induced Photoaging by a TNFR Antagonistic Peptide, TNFR2-SKE.

Authors:  Kyoung-Jin Lee; Kyeong Han Park; Jang-Hee Hahn
Journal:  Mol Cells       Date:  2019-01-24       Impact factor: 5.034

  6 in total

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