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Induction of functional xeno-free MSCs from human iPSCs via a neural crest cell lineage
Mesenchymal stem/stromal cells (MSCs) are adult multipotent stem cells. Here, we induced MSCs from human induced pluripotent stem cells (iPSCs) via a neural crest cell (NCC) lineage under xeno-free conditions and evaluated their in vivo functions. We modified a previous MSC induction method to work...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9477888/ https://www.ncbi.nlm.nih.gov/pubmed/36109564 http://dx.doi.org/10.1038/s41536-022-00241-8 |
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author | Kamiya, Daisuke Takenaka-Ninagawa, Nana Motoike, Souta Kajiya, Mikihito Akaboshi, Teppei Zhao, Chengzhu Shibata, Mitsuaki Senda, Sho Toyooka, Yayoi Sakurai, Hidetoshi Kurihara, Hidemi Ikeya, Makoto |
author_facet | Kamiya, Daisuke Takenaka-Ninagawa, Nana Motoike, Souta Kajiya, Mikihito Akaboshi, Teppei Zhao, Chengzhu Shibata, Mitsuaki Senda, Sho Toyooka, Yayoi Sakurai, Hidetoshi Kurihara, Hidemi Ikeya, Makoto |
author_sort | Kamiya, Daisuke |
collection | PubMed |
description | Mesenchymal stem/stromal cells (MSCs) are adult multipotent stem cells. Here, we induced MSCs from human induced pluripotent stem cells (iPSCs) via a neural crest cell (NCC) lineage under xeno-free conditions and evaluated their in vivo functions. We modified a previous MSC induction method to work under xeno-free conditions. Bovine serum albumin-containing NCC induction medium and fetal bovine serum-containing MSC induction medium were replaced with xeno-free medium. Through our optimized method, iPSCs differentiated into MSCs with high efficiency. To evaluate their in vivo activities, we transplanted the xeno-free-induced MSCs (XF-iMSCs) into mouse models for bone and skeletal muscle regeneration and confirmed their regenerative potency. These XF-iMSCs mainly promoted the regeneration of surrounding host cells, suggesting that they secrete soluble factors into affected regions. We also found that the peroxidasin and IGF2 secreted by the XF-iMSCs partially contributed to myotube differentiation. These results suggest that XF-iMSCs are important for future applications in regenerative medicine. |
format | Online Article Text |
id | pubmed-9477888 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-94778882022-09-17 Induction of functional xeno-free MSCs from human iPSCs via a neural crest cell lineage Kamiya, Daisuke Takenaka-Ninagawa, Nana Motoike, Souta Kajiya, Mikihito Akaboshi, Teppei Zhao, Chengzhu Shibata, Mitsuaki Senda, Sho Toyooka, Yayoi Sakurai, Hidetoshi Kurihara, Hidemi Ikeya, Makoto NPJ Regen Med Article Mesenchymal stem/stromal cells (MSCs) are adult multipotent stem cells. Here, we induced MSCs from human induced pluripotent stem cells (iPSCs) via a neural crest cell (NCC) lineage under xeno-free conditions and evaluated their in vivo functions. We modified a previous MSC induction method to work under xeno-free conditions. Bovine serum albumin-containing NCC induction medium and fetal bovine serum-containing MSC induction medium were replaced with xeno-free medium. Through our optimized method, iPSCs differentiated into MSCs with high efficiency. To evaluate their in vivo activities, we transplanted the xeno-free-induced MSCs (XF-iMSCs) into mouse models for bone and skeletal muscle regeneration and confirmed their regenerative potency. These XF-iMSCs mainly promoted the regeneration of surrounding host cells, suggesting that they secrete soluble factors into affected regions. We also found that the peroxidasin and IGF2 secreted by the XF-iMSCs partially contributed to myotube differentiation. These results suggest that XF-iMSCs are important for future applications in regenerative medicine. Nature Publishing Group UK 2022-09-15 /pmc/articles/PMC9477888/ /pubmed/36109564 http://dx.doi.org/10.1038/s41536-022-00241-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Kamiya, Daisuke Takenaka-Ninagawa, Nana Motoike, Souta Kajiya, Mikihito Akaboshi, Teppei Zhao, Chengzhu Shibata, Mitsuaki Senda, Sho Toyooka, Yayoi Sakurai, Hidetoshi Kurihara, Hidemi Ikeya, Makoto Induction of functional xeno-free MSCs from human iPSCs via a neural crest cell lineage |
title | Induction of functional xeno-free MSCs from human iPSCs via a neural crest cell lineage |
title_full | Induction of functional xeno-free MSCs from human iPSCs via a neural crest cell lineage |
title_fullStr | Induction of functional xeno-free MSCs from human iPSCs via a neural crest cell lineage |
title_full_unstemmed | Induction of functional xeno-free MSCs from human iPSCs via a neural crest cell lineage |
title_short | Induction of functional xeno-free MSCs from human iPSCs via a neural crest cell lineage |
title_sort | induction of functional xeno-free mscs from human ipscs via a neural crest cell lineage |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9477888/ https://www.ncbi.nlm.nih.gov/pubmed/36109564 http://dx.doi.org/10.1038/s41536-022-00241-8 |
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