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Pre-clinical study of induced pluripotent stem cell-derived dopaminergic progenitor cells for Parkinson’s disease
Induced pluripotent stem cell (iPSC)-derived dopaminergic (DA) neurons are an expected source for cell-based therapies for Parkinson’s disease (PD). The regulatory criteria for the clinical application of these therapies, however, have not been established. Here we show the results of our pre-clinic...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7338530/ https://www.ncbi.nlm.nih.gov/pubmed/32632153 http://dx.doi.org/10.1038/s41467-020-17165-w |
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author | Doi, Daisuke Magotani, Hiroaki Kikuchi, Tetsuhiro Ikeda, Megumi Hiramatsu, Satoe Yoshida, Kenji Amano, Naoki Nomura, Masaki Umekage, Masafumi Morizane, Asuka Takahashi, Jun |
author_facet | Doi, Daisuke Magotani, Hiroaki Kikuchi, Tetsuhiro Ikeda, Megumi Hiramatsu, Satoe Yoshida, Kenji Amano, Naoki Nomura, Masaki Umekage, Masafumi Morizane, Asuka Takahashi, Jun |
author_sort | Doi, Daisuke |
collection | PubMed |
description | Induced pluripotent stem cell (iPSC)-derived dopaminergic (DA) neurons are an expected source for cell-based therapies for Parkinson’s disease (PD). The regulatory criteria for the clinical application of these therapies, however, have not been established. Here we show the results of our pre-clinical study, in which we evaluate the safety and efficacy of dopaminergic progenitors (DAPs) derived from a clinical-grade human iPSC line. We confirm the characteristics of DAPs by in vitro analyses. We also verify that the DAP population include no residual undifferentiated iPSCs or early neural stem cells and have no genetic aberration in cancer-related genes. Furthermore, in vivo studies using immunodeficient mice reveal no tumorigenicity or toxicity of the cells. When the DAPs are transplanted into the striatum of 6-OHDA-lesioned rats, the animals show behavioral improvement. Based on these results, we started a clinical trial to treat PD patients in 2018. |
format | Online Article Text |
id | pubmed-7338530 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73385302020-07-09 Pre-clinical study of induced pluripotent stem cell-derived dopaminergic progenitor cells for Parkinson’s disease Doi, Daisuke Magotani, Hiroaki Kikuchi, Tetsuhiro Ikeda, Megumi Hiramatsu, Satoe Yoshida, Kenji Amano, Naoki Nomura, Masaki Umekage, Masafumi Morizane, Asuka Takahashi, Jun Nat Commun Article Induced pluripotent stem cell (iPSC)-derived dopaminergic (DA) neurons are an expected source for cell-based therapies for Parkinson’s disease (PD). The regulatory criteria for the clinical application of these therapies, however, have not been established. Here we show the results of our pre-clinical study, in which we evaluate the safety and efficacy of dopaminergic progenitors (DAPs) derived from a clinical-grade human iPSC line. We confirm the characteristics of DAPs by in vitro analyses. We also verify that the DAP population include no residual undifferentiated iPSCs or early neural stem cells and have no genetic aberration in cancer-related genes. Furthermore, in vivo studies using immunodeficient mice reveal no tumorigenicity or toxicity of the cells. When the DAPs are transplanted into the striatum of 6-OHDA-lesioned rats, the animals show behavioral improvement. Based on these results, we started a clinical trial to treat PD patients in 2018. Nature Publishing Group UK 2020-07-06 /pmc/articles/PMC7338530/ /pubmed/32632153 http://dx.doi.org/10.1038/s41467-020-17165-w Text en © The Author(s) 2020 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 Doi, Daisuke Magotani, Hiroaki Kikuchi, Tetsuhiro Ikeda, Megumi Hiramatsu, Satoe Yoshida, Kenji Amano, Naoki Nomura, Masaki Umekage, Masafumi Morizane, Asuka Takahashi, Jun Pre-clinical study of induced pluripotent stem cell-derived dopaminergic progenitor cells for Parkinson’s disease |
title | Pre-clinical study of induced pluripotent stem cell-derived dopaminergic progenitor cells for Parkinson’s disease |
title_full | Pre-clinical study of induced pluripotent stem cell-derived dopaminergic progenitor cells for Parkinson’s disease |
title_fullStr | Pre-clinical study of induced pluripotent stem cell-derived dopaminergic progenitor cells for Parkinson’s disease |
title_full_unstemmed | Pre-clinical study of induced pluripotent stem cell-derived dopaminergic progenitor cells for Parkinson’s disease |
title_short | Pre-clinical study of induced pluripotent stem cell-derived dopaminergic progenitor cells for Parkinson’s disease |
title_sort | pre-clinical study of induced pluripotent stem cell-derived dopaminergic progenitor cells for parkinson’s disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7338530/ https://www.ncbi.nlm.nih.gov/pubmed/32632153 http://dx.doi.org/10.1038/s41467-020-17165-w |
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