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Pretreatment with a γ-Secretase Inhibitor Prevents Tumor-like Overgrowth in Human iPSC-Derived Transplants for Spinal Cord Injury
Neural stem/progenitor cells (NS/PCs) derived from human induced pluripotent stem cells (hiPSCs) are considered to be a promising cell source for cell-based interventions that target CNS disorders. We previously reported that transplanting certain hiPSC-NS/PCs in the spinal cord results in tumor-lik...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5063571/ https://www.ncbi.nlm.nih.gov/pubmed/27666789 http://dx.doi.org/10.1016/j.stemcr.2016.08.015 |
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author | Okubo, Toshiki Iwanami, Akio Kohyama, Jun Itakura, Go Kawabata, Soya Nishiyama, Yuichiro Sugai, Keiko Ozaki, Masahiro Iida, Tsuyoshi Matsubayashi, Kohei Matsumoto, Morio Nakamura, Masaya Okano, Hideyuki |
author_facet | Okubo, Toshiki Iwanami, Akio Kohyama, Jun Itakura, Go Kawabata, Soya Nishiyama, Yuichiro Sugai, Keiko Ozaki, Masahiro Iida, Tsuyoshi Matsubayashi, Kohei Matsumoto, Morio Nakamura, Masaya Okano, Hideyuki |
author_sort | Okubo, Toshiki |
collection | PubMed |
description | Neural stem/progenitor cells (NS/PCs) derived from human induced pluripotent stem cells (hiPSCs) are considered to be a promising cell source for cell-based interventions that target CNS disorders. We previously reported that transplanting certain hiPSC-NS/PCs in the spinal cord results in tumor-like overgrowth of hiPSC-NS/PCs and subsequent deterioration of motor function. Remnant immature cells should be removed or induced into more mature cell types to avoid adverse effects of hiPSC-NS/PC transplantation. Because Notch signaling plays a role in maintaining NS/PCs, we evaluated the effects of γ-secretase inhibitor (GSI) and found that pretreating hiPSC-NS/PCs with GSI promoted neuronal differentiation and maturation in vitro, and GSI pretreatment also reduced the overgrowth of transplanted hiPSC-NS/PCs and inhibited the deterioration of motor function in vivo. These results indicate that pretreatment with hiPSC-NS/PCs decreases the proliferative capacity of transplanted hiPSC-NS/PCs, triggers neuronal commitment, and improves the safety of hiPSC-based approaches in regenerative medicine. |
format | Online Article Text |
id | pubmed-5063571 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-50635712016-10-19 Pretreatment with a γ-Secretase Inhibitor Prevents Tumor-like Overgrowth in Human iPSC-Derived Transplants for Spinal Cord Injury Okubo, Toshiki Iwanami, Akio Kohyama, Jun Itakura, Go Kawabata, Soya Nishiyama, Yuichiro Sugai, Keiko Ozaki, Masahiro Iida, Tsuyoshi Matsubayashi, Kohei Matsumoto, Morio Nakamura, Masaya Okano, Hideyuki Stem Cell Reports Article Neural stem/progenitor cells (NS/PCs) derived from human induced pluripotent stem cells (hiPSCs) are considered to be a promising cell source for cell-based interventions that target CNS disorders. We previously reported that transplanting certain hiPSC-NS/PCs in the spinal cord results in tumor-like overgrowth of hiPSC-NS/PCs and subsequent deterioration of motor function. Remnant immature cells should be removed or induced into more mature cell types to avoid adverse effects of hiPSC-NS/PC transplantation. Because Notch signaling plays a role in maintaining NS/PCs, we evaluated the effects of γ-secretase inhibitor (GSI) and found that pretreating hiPSC-NS/PCs with GSI promoted neuronal differentiation and maturation in vitro, and GSI pretreatment also reduced the overgrowth of transplanted hiPSC-NS/PCs and inhibited the deterioration of motor function in vivo. These results indicate that pretreatment with hiPSC-NS/PCs decreases the proliferative capacity of transplanted hiPSC-NS/PCs, triggers neuronal commitment, and improves the safety of hiPSC-based approaches in regenerative medicine. Elsevier 2016-09-22 /pmc/articles/PMC5063571/ /pubmed/27666789 http://dx.doi.org/10.1016/j.stemcr.2016.08.015 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Okubo, Toshiki Iwanami, Akio Kohyama, Jun Itakura, Go Kawabata, Soya Nishiyama, Yuichiro Sugai, Keiko Ozaki, Masahiro Iida, Tsuyoshi Matsubayashi, Kohei Matsumoto, Morio Nakamura, Masaya Okano, Hideyuki Pretreatment with a γ-Secretase Inhibitor Prevents Tumor-like Overgrowth in Human iPSC-Derived Transplants for Spinal Cord Injury |
title | Pretreatment with a γ-Secretase Inhibitor Prevents Tumor-like Overgrowth in Human iPSC-Derived Transplants for Spinal Cord Injury |
title_full | Pretreatment with a γ-Secretase Inhibitor Prevents Tumor-like Overgrowth in Human iPSC-Derived Transplants for Spinal Cord Injury |
title_fullStr | Pretreatment with a γ-Secretase Inhibitor Prevents Tumor-like Overgrowth in Human iPSC-Derived Transplants for Spinal Cord Injury |
title_full_unstemmed | Pretreatment with a γ-Secretase Inhibitor Prevents Tumor-like Overgrowth in Human iPSC-Derived Transplants for Spinal Cord Injury |
title_short | Pretreatment with a γ-Secretase Inhibitor Prevents Tumor-like Overgrowth in Human iPSC-Derived Transplants for Spinal Cord Injury |
title_sort | pretreatment with a γ-secretase inhibitor prevents tumor-like overgrowth in human ipsc-derived transplants for spinal cord injury |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5063571/ https://www.ncbi.nlm.nih.gov/pubmed/27666789 http://dx.doi.org/10.1016/j.stemcr.2016.08.015 |
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