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Mesenchymal–epithelial interactions in the skin: increased expression of dickkopf1 by palmoplantar fibroblasts inhibits melanocyte growth and differentiation

We investigated whether or not the topographic regulation of melanocyte differentiation is determined by mesenchymal–epithelial interactions via fibroblast-derived factors. The melanocyte density in palmoplantar human skin (i.e., skin on the palms and the soles) is five times lower than that found i...

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Autores principales: Yamaguchi, Yuji, Itami, Satoshi, Watabe, Hidenori, Yasumoto, Ken-ichi, Abdel-Malek, Zalfa A., Kubo, Tateki, Rouzaud, François, Tanemura, Atsushi, Yoshikawa, Kunihiko, Hearing, Vincent J.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2172049/
https://www.ncbi.nlm.nih.gov/pubmed/15117970
http://dx.doi.org/10.1083/jcb.200311122
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author Yamaguchi, Yuji
Itami, Satoshi
Watabe, Hidenori
Yasumoto, Ken-ichi
Abdel-Malek, Zalfa A.
Kubo, Tateki
Rouzaud, François
Tanemura, Atsushi
Yoshikawa, Kunihiko
Hearing, Vincent J.
author_facet Yamaguchi, Yuji
Itami, Satoshi
Watabe, Hidenori
Yasumoto, Ken-ichi
Abdel-Malek, Zalfa A.
Kubo, Tateki
Rouzaud, François
Tanemura, Atsushi
Yoshikawa, Kunihiko
Hearing, Vincent J.
author_sort Yamaguchi, Yuji
collection PubMed
description We investigated whether or not the topographic regulation of melanocyte differentiation is determined by mesenchymal–epithelial interactions via fibroblast-derived factors. The melanocyte density in palmoplantar human skin (i.e., skin on the palms and the soles) is five times lower than that found in nonpalmoplantar sites. Palmoplantar fibroblasts significantly suppressed the growth and pigmentation of melanocytes compared with nonpalmoplantar fibroblasts. Using cDNA microarray analysis, fibroblasts derived from palmoplantar skin expressed high levels of dickkopf 1 (DKK1; an inhibitor of the canonical Wnt signaling pathway), whereas nonpalmoplantar fibroblasts expressed higher levels of DKK3. Transfection studies revealed that DKK1 decreased melanocyte function, probably through β-catenin–mediated regulation of microphthalmia-associated transcription factor activity, which in turn modulates the growth and differentiation of melanocytes. Thus, our results provide a basis to explain why skin on the palms and the soles is generally hypopigmented compared with other areas of the body, and might explain why melanocytes stop migrating in the palmoplantar area during human embryogenesis.
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spelling pubmed-21720492008-03-05 Mesenchymal–epithelial interactions in the skin: increased expression of dickkopf1 by palmoplantar fibroblasts inhibits melanocyte growth and differentiation Yamaguchi, Yuji Itami, Satoshi Watabe, Hidenori Yasumoto, Ken-ichi Abdel-Malek, Zalfa A. Kubo, Tateki Rouzaud, François Tanemura, Atsushi Yoshikawa, Kunihiko Hearing, Vincent J. J Cell Biol Article We investigated whether or not the topographic regulation of melanocyte differentiation is determined by mesenchymal–epithelial interactions via fibroblast-derived factors. The melanocyte density in palmoplantar human skin (i.e., skin on the palms and the soles) is five times lower than that found in nonpalmoplantar sites. Palmoplantar fibroblasts significantly suppressed the growth and pigmentation of melanocytes compared with nonpalmoplantar fibroblasts. Using cDNA microarray analysis, fibroblasts derived from palmoplantar skin expressed high levels of dickkopf 1 (DKK1; an inhibitor of the canonical Wnt signaling pathway), whereas nonpalmoplantar fibroblasts expressed higher levels of DKK3. Transfection studies revealed that DKK1 decreased melanocyte function, probably through β-catenin–mediated regulation of microphthalmia-associated transcription factor activity, which in turn modulates the growth and differentiation of melanocytes. Thus, our results provide a basis to explain why skin on the palms and the soles is generally hypopigmented compared with other areas of the body, and might explain why melanocytes stop migrating in the palmoplantar area during human embryogenesis. The Rockefeller University Press 2004-04-26 /pmc/articles/PMC2172049/ /pubmed/15117970 http://dx.doi.org/10.1083/jcb.200311122 Text en Copyright © 2004, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Yamaguchi, Yuji
Itami, Satoshi
Watabe, Hidenori
Yasumoto, Ken-ichi
Abdel-Malek, Zalfa A.
Kubo, Tateki
Rouzaud, François
Tanemura, Atsushi
Yoshikawa, Kunihiko
Hearing, Vincent J.
Mesenchymal–epithelial interactions in the skin: increased expression of dickkopf1 by palmoplantar fibroblasts inhibits melanocyte growth and differentiation
title Mesenchymal–epithelial interactions in the skin: increased expression of dickkopf1 by palmoplantar fibroblasts inhibits melanocyte growth and differentiation
title_full Mesenchymal–epithelial interactions in the skin: increased expression of dickkopf1 by palmoplantar fibroblasts inhibits melanocyte growth and differentiation
title_fullStr Mesenchymal–epithelial interactions in the skin: increased expression of dickkopf1 by palmoplantar fibroblasts inhibits melanocyte growth and differentiation
title_full_unstemmed Mesenchymal–epithelial interactions in the skin: increased expression of dickkopf1 by palmoplantar fibroblasts inhibits melanocyte growth and differentiation
title_short Mesenchymal–epithelial interactions in the skin: increased expression of dickkopf1 by palmoplantar fibroblasts inhibits melanocyte growth and differentiation
title_sort mesenchymal–epithelial interactions in the skin: increased expression of dickkopf1 by palmoplantar fibroblasts inhibits melanocyte growth and differentiation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2172049/
https://www.ncbi.nlm.nih.gov/pubmed/15117970
http://dx.doi.org/10.1083/jcb.200311122
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