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Derivation of induced pluripotent stem cells in Japanese macaque (Macaca fuscata)

Non-human primates are our closest relatives and are of special interest for ecological, evolutionary and biomedical research. The Japanese macaque (Macaca fuscata) has contributed to the progress of primatology and neurosciences over 60 years. Despite this importance, the molecular and cellular bas...

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Autores principales: Nakai, Risako, Ohnuki, Mari, Kuroki, Kota, Ito, Haruka, Hirai, Hirohisa, Kitajima, Ryunosuke, Fujimoto, Toko, Nakagawa, Masato, Enard, Wolfgang, Imamura, Masanori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6093926/
https://www.ncbi.nlm.nih.gov/pubmed/30111816
http://dx.doi.org/10.1038/s41598-018-30734-w
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author Nakai, Risako
Ohnuki, Mari
Kuroki, Kota
Ito, Haruka
Hirai, Hirohisa
Kitajima, Ryunosuke
Fujimoto, Toko
Nakagawa, Masato
Enard, Wolfgang
Imamura, Masanori
author_facet Nakai, Risako
Ohnuki, Mari
Kuroki, Kota
Ito, Haruka
Hirai, Hirohisa
Kitajima, Ryunosuke
Fujimoto, Toko
Nakagawa, Masato
Enard, Wolfgang
Imamura, Masanori
author_sort Nakai, Risako
collection PubMed
description Non-human primates are our closest relatives and are of special interest for ecological, evolutionary and biomedical research. The Japanese macaque (Macaca fuscata) has contributed to the progress of primatology and neurosciences over 60 years. Despite this importance, the molecular and cellular basis of the Japanese macaque remains unexplored since useful cellular tools are lacking. Here we generated induced pluripotent stem cells (iPSCs) from skin fibroblasts of the Japanese macaque with Sendai virus or plasmid vectors. The Japanese macaque iPSCs (jm-iPSCs) were established under feeder-free culture conditions, but feeder cells turned out to be essential for their maintenance. The jm-iPSCs formed human iPSC-like flat colonies which were positive for pluripotent antigens including alkaline phosphatase, SSEA4, and TRA-1-81. They also expressed endogenous OCT3/4, SOX2, L-MYC, and KLF4 and other pluripotent marker genes. The potential to differentiate into all three germ layers and neural stem cells was confirmed by embryoid body and neurosphere formation, respectively. The jm-iPSCs will provide a robust in vitro tool for investigating the underlying mechanisms of development and physiology studies with the Japanese macaque.
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spelling pubmed-60939262018-08-20 Derivation of induced pluripotent stem cells in Japanese macaque (Macaca fuscata) Nakai, Risako Ohnuki, Mari Kuroki, Kota Ito, Haruka Hirai, Hirohisa Kitajima, Ryunosuke Fujimoto, Toko Nakagawa, Masato Enard, Wolfgang Imamura, Masanori Sci Rep Article Non-human primates are our closest relatives and are of special interest for ecological, evolutionary and biomedical research. The Japanese macaque (Macaca fuscata) has contributed to the progress of primatology and neurosciences over 60 years. Despite this importance, the molecular and cellular basis of the Japanese macaque remains unexplored since useful cellular tools are lacking. Here we generated induced pluripotent stem cells (iPSCs) from skin fibroblasts of the Japanese macaque with Sendai virus or plasmid vectors. The Japanese macaque iPSCs (jm-iPSCs) were established under feeder-free culture conditions, but feeder cells turned out to be essential for their maintenance. The jm-iPSCs formed human iPSC-like flat colonies which were positive for pluripotent antigens including alkaline phosphatase, SSEA4, and TRA-1-81. They also expressed endogenous OCT3/4, SOX2, L-MYC, and KLF4 and other pluripotent marker genes. The potential to differentiate into all three germ layers and neural stem cells was confirmed by embryoid body and neurosphere formation, respectively. The jm-iPSCs will provide a robust in vitro tool for investigating the underlying mechanisms of development and physiology studies with the Japanese macaque. Nature Publishing Group UK 2018-08-15 /pmc/articles/PMC6093926/ /pubmed/30111816 http://dx.doi.org/10.1038/s41598-018-30734-w Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Nakai, Risako
Ohnuki, Mari
Kuroki, Kota
Ito, Haruka
Hirai, Hirohisa
Kitajima, Ryunosuke
Fujimoto, Toko
Nakagawa, Masato
Enard, Wolfgang
Imamura, Masanori
Derivation of induced pluripotent stem cells in Japanese macaque (Macaca fuscata)
title Derivation of induced pluripotent stem cells in Japanese macaque (Macaca fuscata)
title_full Derivation of induced pluripotent stem cells in Japanese macaque (Macaca fuscata)
title_fullStr Derivation of induced pluripotent stem cells in Japanese macaque (Macaca fuscata)
title_full_unstemmed Derivation of induced pluripotent stem cells in Japanese macaque (Macaca fuscata)
title_short Derivation of induced pluripotent stem cells in Japanese macaque (Macaca fuscata)
title_sort derivation of induced pluripotent stem cells in japanese macaque (macaca fuscata)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6093926/
https://www.ncbi.nlm.nih.gov/pubmed/30111816
http://dx.doi.org/10.1038/s41598-018-30734-w
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