Generation of human melanocytes from induced pluripotent stem cells.

Epidermal melanocytes play an important role in protecting the skin from UV rays, and their functional impairment results in pigment disorders. Additionally, melanomas are considered to arise from mutations that accumulate in melanocyte stem cells. The mechanisms underlying melanocyte differentiatio...

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Autores principales: Shigeki Ohta, Yoichi Imaizumi, Yohei Okada, Wado Akamatsu, Reiko Kuwahara, Manabu Ohyama, Masayuki Amagai, Yumi Matsuzaki, Shinya Yamanaka, Hideyuki Okano, Yutaka Kawakami
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Publicado: Public Library of Science (PLoS) 2011
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Acceso en línea:https://doaj.org/article/360cbd18bfe44ad7a4b777094a9f94c6
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spelling oai:doaj.org-article:360cbd18bfe44ad7a4b777094a9f94c62021-11-18T07:00:30ZGeneration of human melanocytes from induced pluripotent stem cells.1932-620310.1371/journal.pone.0016182https://doaj.org/article/360cbd18bfe44ad7a4b777094a9f94c62011-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21249204/?tool=EBIhttps://doaj.org/toc/1932-6203Epidermal melanocytes play an important role in protecting the skin from UV rays, and their functional impairment results in pigment disorders. Additionally, melanomas are considered to arise from mutations that accumulate in melanocyte stem cells. The mechanisms underlying melanocyte differentiation and the defining characteristics of melanocyte stem cells in humans are, however, largely unknown. In the present study, we set out to generate melanocytes from human iPS cells in vitro, leading to a preliminary investigation of the mechanisms of human melanocyte differentiation. We generated iPS cell lines from human dermal fibroblasts using the Yamanaka factors (SOX2, OCT3/4, and KLF4, with or without c-MYC). These iPS cell lines were subsequently used to form embryoid bodies (EBs) and then differentiated into melanocytes via culture supplementation with Wnt3a, SCF, and ET-3. Seven weeks after inducing differentiation, pigmented cells expressing melanocyte markers such as MITF, tyrosinase, SILV, and TYRP1, were detected. Melanosomes were identified in these pigmented cells by electron microscopy, and global gene expression profiling of the pigmented cells showed a high similarity to that of human primary foreskin-derived melanocytes, suggesting the successful generation of melanocytes from iPS cells. This in vitro differentiation system should prove useful for understanding human melanocyte biology and revealing the mechanism of various pigment cell disorders, including melanoma.Shigeki OhtaYoichi ImaizumiYohei OkadaWado AkamatsuReiko KuwaharaManabu OhyamaMasayuki AmagaiYumi MatsuzakiShinya YamanakaHideyuki OkanoYutaka KawakamiPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 6, Iss 1, p e16182 (2011)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Shigeki Ohta
Yoichi Imaizumi
Yohei Okada
Wado Akamatsu
Reiko Kuwahara
Manabu Ohyama
Masayuki Amagai
Yumi Matsuzaki
Shinya Yamanaka
Hideyuki Okano
Yutaka Kawakami
Generation of human melanocytes from induced pluripotent stem cells.
description Epidermal melanocytes play an important role in protecting the skin from UV rays, and their functional impairment results in pigment disorders. Additionally, melanomas are considered to arise from mutations that accumulate in melanocyte stem cells. The mechanisms underlying melanocyte differentiation and the defining characteristics of melanocyte stem cells in humans are, however, largely unknown. In the present study, we set out to generate melanocytes from human iPS cells in vitro, leading to a preliminary investigation of the mechanisms of human melanocyte differentiation. We generated iPS cell lines from human dermal fibroblasts using the Yamanaka factors (SOX2, OCT3/4, and KLF4, with or without c-MYC). These iPS cell lines were subsequently used to form embryoid bodies (EBs) and then differentiated into melanocytes via culture supplementation with Wnt3a, SCF, and ET-3. Seven weeks after inducing differentiation, pigmented cells expressing melanocyte markers such as MITF, tyrosinase, SILV, and TYRP1, were detected. Melanosomes were identified in these pigmented cells by electron microscopy, and global gene expression profiling of the pigmented cells showed a high similarity to that of human primary foreskin-derived melanocytes, suggesting the successful generation of melanocytes from iPS cells. This in vitro differentiation system should prove useful for understanding human melanocyte biology and revealing the mechanism of various pigment cell disorders, including melanoma.
format article
author Shigeki Ohta
Yoichi Imaizumi
Yohei Okada
Wado Akamatsu
Reiko Kuwahara
Manabu Ohyama
Masayuki Amagai
Yumi Matsuzaki
Shinya Yamanaka
Hideyuki Okano
Yutaka Kawakami
author_facet Shigeki Ohta
Yoichi Imaizumi
Yohei Okada
Wado Akamatsu
Reiko Kuwahara
Manabu Ohyama
Masayuki Amagai
Yumi Matsuzaki
Shinya Yamanaka
Hideyuki Okano
Yutaka Kawakami
author_sort Shigeki Ohta
title Generation of human melanocytes from induced pluripotent stem cells.
title_short Generation of human melanocytes from induced pluripotent stem cells.
title_full Generation of human melanocytes from induced pluripotent stem cells.
title_fullStr Generation of human melanocytes from induced pluripotent stem cells.
title_full_unstemmed Generation of human melanocytes from induced pluripotent stem cells.
title_sort generation of human melanocytes from induced pluripotent stem cells.
publisher Public Library of Science (PLoS)
publishDate 2011
url https://doaj.org/article/360cbd18bfe44ad7a4b777094a9f94c6
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