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Stepwise strategy for generating osteoblasts from human pluripotent stem cells under fully defined xeno-free conditions with small-molecule inducers
Clinically relevant human induced pluripotent stem cell (hiPSC) derivatives require efficient protocols to differentiate hiPSCs into specific lineages. Here we developed a fully defined xeno-free strategy to direct hiPSCs toward osteoblasts within 21 days. The strategy successfully achieved the oste...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Japanese Society for Regenerative Medicine
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6965656/ https://www.ncbi.nlm.nih.gov/pubmed/31988991 http://dx.doi.org/10.1016/j.reth.2019.12.010 |
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author | Zujur, Denise Kanke, Kosuke Onodera, Shoko Tani, Shoichiro Lai, Jenny Azuma, Toshifumi Xin, Xiaonan Lichtler, Alexander C. Rowe, David W. Saito, Taku Tanaka, Sakae Masaki, Hideki Nakauchi, Hiromitsu Chung, Ung-il Hojo, Hironori Ohba, Shinsuke |
author_facet | Zujur, Denise Kanke, Kosuke Onodera, Shoko Tani, Shoichiro Lai, Jenny Azuma, Toshifumi Xin, Xiaonan Lichtler, Alexander C. Rowe, David W. Saito, Taku Tanaka, Sakae Masaki, Hideki Nakauchi, Hiromitsu Chung, Ung-il Hojo, Hironori Ohba, Shinsuke |
author_sort | Zujur, Denise |
collection | PubMed |
description | Clinically relevant human induced pluripotent stem cell (hiPSC) derivatives require efficient protocols to differentiate hiPSCs into specific lineages. Here we developed a fully defined xeno-free strategy to direct hiPSCs toward osteoblasts within 21 days. The strategy successfully achieved the osteogenic induction of four independently derived hiPSC lines by a sequential use of combinations of small-molecule inducers. The induction first generated mesodermal cells, which subsequently recapitulated the developmental expression pattern of major osteoblast genes and proteins. Importantly, Col2.3-Cherry hiPSCs subjected to this strategy strongly expressed the cherry fluorescence that has been observed in bone-forming osteoblasts in vivo. Moreover, the protocol combined with a three-dimensional (3D) scaffold was suitable for the generation of a xeno-free 3D osteogenic system. Thus, our strategy offers a platform with significant advantages for bone biology studies and it will also contribute to clinical applications of hiPSCs to skeletal regenerative medicine. |
format | Online Article Text |
id | pubmed-6965656 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Japanese Society for Regenerative Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-69656562020-01-27 Stepwise strategy for generating osteoblasts from human pluripotent stem cells under fully defined xeno-free conditions with small-molecule inducers Zujur, Denise Kanke, Kosuke Onodera, Shoko Tani, Shoichiro Lai, Jenny Azuma, Toshifumi Xin, Xiaonan Lichtler, Alexander C. Rowe, David W. Saito, Taku Tanaka, Sakae Masaki, Hideki Nakauchi, Hiromitsu Chung, Ung-il Hojo, Hironori Ohba, Shinsuke Regen Ther Original Article Clinically relevant human induced pluripotent stem cell (hiPSC) derivatives require efficient protocols to differentiate hiPSCs into specific lineages. Here we developed a fully defined xeno-free strategy to direct hiPSCs toward osteoblasts within 21 days. The strategy successfully achieved the osteogenic induction of four independently derived hiPSC lines by a sequential use of combinations of small-molecule inducers. The induction first generated mesodermal cells, which subsequently recapitulated the developmental expression pattern of major osteoblast genes and proteins. Importantly, Col2.3-Cherry hiPSCs subjected to this strategy strongly expressed the cherry fluorescence that has been observed in bone-forming osteoblasts in vivo. Moreover, the protocol combined with a three-dimensional (3D) scaffold was suitable for the generation of a xeno-free 3D osteogenic system. Thus, our strategy offers a platform with significant advantages for bone biology studies and it will also contribute to clinical applications of hiPSCs to skeletal regenerative medicine. Japanese Society for Regenerative Medicine 2020-01-14 /pmc/articles/PMC6965656/ /pubmed/31988991 http://dx.doi.org/10.1016/j.reth.2019.12.010 Text en © 2020 The Japanese Society for Regenerative Medicine. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Zujur, Denise Kanke, Kosuke Onodera, Shoko Tani, Shoichiro Lai, Jenny Azuma, Toshifumi Xin, Xiaonan Lichtler, Alexander C. Rowe, David W. Saito, Taku Tanaka, Sakae Masaki, Hideki Nakauchi, Hiromitsu Chung, Ung-il Hojo, Hironori Ohba, Shinsuke Stepwise strategy for generating osteoblasts from human pluripotent stem cells under fully defined xeno-free conditions with small-molecule inducers |
title | Stepwise strategy for generating osteoblasts from human pluripotent stem cells under fully defined xeno-free conditions with small-molecule inducers |
title_full | Stepwise strategy for generating osteoblasts from human pluripotent stem cells under fully defined xeno-free conditions with small-molecule inducers |
title_fullStr | Stepwise strategy for generating osteoblasts from human pluripotent stem cells under fully defined xeno-free conditions with small-molecule inducers |
title_full_unstemmed | Stepwise strategy for generating osteoblasts from human pluripotent stem cells under fully defined xeno-free conditions with small-molecule inducers |
title_short | Stepwise strategy for generating osteoblasts from human pluripotent stem cells under fully defined xeno-free conditions with small-molecule inducers |
title_sort | stepwise strategy for generating osteoblasts from human pluripotent stem cells under fully defined xeno-free conditions with small-molecule inducers |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6965656/ https://www.ncbi.nlm.nih.gov/pubmed/31988991 http://dx.doi.org/10.1016/j.reth.2019.12.010 |
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