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In vivo monitoring of remnant undifferentiated neural cells following human induced pluripotent stem cell‐derived neural stem/progenitor cells transplantation
Transplantation of human‐induced pluripotent stem cell‐derived neural stem/progenitor cells (hiPSC‐NS/PCs) is a promising treatment for a variety of neuropathological conditions. Although previous reports have indicated the effectiveness of hiPSC‐NS/PCs transplantation into the injured spinal cord o...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7103627/ https://www.ncbi.nlm.nih.gov/pubmed/31904914 http://dx.doi.org/10.1002/sctm.19-0150 |
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author | Tanimoto, Yuji Yamasaki, Tomoteru Nagoshi, Narihito Nishiyama, Yuichiro Nori, Satoshi Nishimura, Soraya Iida, Tsuyoshi Ozaki, Masahiro Tsuji, Osahiko Ji, Bin Aoki, Ichio Jinzaki, Masahiro Matsumoto, Morio Fujibayashi, Yasuhisa Zhang, Ming‐Rong Nakamura, Masaya Okano, Hideyuki |
author_facet | Tanimoto, Yuji Yamasaki, Tomoteru Nagoshi, Narihito Nishiyama, Yuichiro Nori, Satoshi Nishimura, Soraya Iida, Tsuyoshi Ozaki, Masahiro Tsuji, Osahiko Ji, Bin Aoki, Ichio Jinzaki, Masahiro Matsumoto, Morio Fujibayashi, Yasuhisa Zhang, Ming‐Rong Nakamura, Masaya Okano, Hideyuki |
author_sort | Tanimoto, Yuji |
collection | PubMed |
description | Transplantation of human‐induced pluripotent stem cell‐derived neural stem/progenitor cells (hiPSC‐NS/PCs) is a promising treatment for a variety of neuropathological conditions. Although previous reports have indicated the effectiveness of hiPSC‐NS/PCs transplantation into the injured spinal cord of rodents and nonhuman primates, long‐term observation of hiPSC‐NS/PCs post‐transplantation suggested some “unsafe” differentiation‐resistant properties, resulting in disordered overgrowth. These findings suggest that, even if “safe” NS/PCs are transplanted into the human central nervous system (CNS), the dynamics of cellular differentiation of stem cells should be noninvasively tracked to ensure safety. Positron emission tomography (PET) provides molecular‐functional information and helps to detect specific disease conditions. The current study was conducted to visualize Nestin (an NS/PC marker)‐positive undifferentiated neural cells in the CNS of immune‐deficient (nonobese diabetic‐severe combined immune‐deficient) mice after hiPSC‐NS/PCs transplantation with PET, using 18 kDa translocator protein (TSPO) ligands as labels. TSPO was recently found to be expressed in rodent NS/PCs, and its expression decreased with the progression of neuronal differentiation. We hypothesized that TSPO would also be present in hiPSC‐NS/PCs and expressed strongly in residual immature neural cells after transplantation. The results showed high levels of TSPO expression in immature hiPSC‐NS/PCs‐derived cells, and decreased TSPO expression as neural differentiation progressed in vitro. Furthermore, PET with [(18)F] FEDAC (a TSPO radioligand) was able to visualize the remnant undifferentiated hiPSC‐NS/PCs‐derived cells consisting of TSPO and Nestin(+) cells in vivo. These findings suggest that PET with [(18)F] FEDAC could play a key role in the safe clinical application of CNS repair in regenerative medicine. |
format | Online Article Text |
id | pubmed-7103627 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71036272020-03-31 In vivo monitoring of remnant undifferentiated neural cells following human induced pluripotent stem cell‐derived neural stem/progenitor cells transplantation Tanimoto, Yuji Yamasaki, Tomoteru Nagoshi, Narihito Nishiyama, Yuichiro Nori, Satoshi Nishimura, Soraya Iida, Tsuyoshi Ozaki, Masahiro Tsuji, Osahiko Ji, Bin Aoki, Ichio Jinzaki, Masahiro Matsumoto, Morio Fujibayashi, Yasuhisa Zhang, Ming‐Rong Nakamura, Masaya Okano, Hideyuki Stem Cells Transl Med Enabling Technologies for Cell‐based Clinical Translation Transplantation of human‐induced pluripotent stem cell‐derived neural stem/progenitor cells (hiPSC‐NS/PCs) is a promising treatment for a variety of neuropathological conditions. Although previous reports have indicated the effectiveness of hiPSC‐NS/PCs transplantation into the injured spinal cord of rodents and nonhuman primates, long‐term observation of hiPSC‐NS/PCs post‐transplantation suggested some “unsafe” differentiation‐resistant properties, resulting in disordered overgrowth. These findings suggest that, even if “safe” NS/PCs are transplanted into the human central nervous system (CNS), the dynamics of cellular differentiation of stem cells should be noninvasively tracked to ensure safety. Positron emission tomography (PET) provides molecular‐functional information and helps to detect specific disease conditions. The current study was conducted to visualize Nestin (an NS/PC marker)‐positive undifferentiated neural cells in the CNS of immune‐deficient (nonobese diabetic‐severe combined immune‐deficient) mice after hiPSC‐NS/PCs transplantation with PET, using 18 kDa translocator protein (TSPO) ligands as labels. TSPO was recently found to be expressed in rodent NS/PCs, and its expression decreased with the progression of neuronal differentiation. We hypothesized that TSPO would also be present in hiPSC‐NS/PCs and expressed strongly in residual immature neural cells after transplantation. The results showed high levels of TSPO expression in immature hiPSC‐NS/PCs‐derived cells, and decreased TSPO expression as neural differentiation progressed in vitro. Furthermore, PET with [(18)F] FEDAC (a TSPO radioligand) was able to visualize the remnant undifferentiated hiPSC‐NS/PCs‐derived cells consisting of TSPO and Nestin(+) cells in vivo. These findings suggest that PET with [(18)F] FEDAC could play a key role in the safe clinical application of CNS repair in regenerative medicine. John Wiley & Sons, Inc. 2020-01-06 /pmc/articles/PMC7103627/ /pubmed/31904914 http://dx.doi.org/10.1002/sctm.19-0150 Text en © 2020 The Authors. stem cells translational medicine published by Wiley Periodicals, Inc. on behalf of AlphaMed Press This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Enabling Technologies for Cell‐based Clinical Translation Tanimoto, Yuji Yamasaki, Tomoteru Nagoshi, Narihito Nishiyama, Yuichiro Nori, Satoshi Nishimura, Soraya Iida, Tsuyoshi Ozaki, Masahiro Tsuji, Osahiko Ji, Bin Aoki, Ichio Jinzaki, Masahiro Matsumoto, Morio Fujibayashi, Yasuhisa Zhang, Ming‐Rong Nakamura, Masaya Okano, Hideyuki In vivo monitoring of remnant undifferentiated neural cells following human induced pluripotent stem cell‐derived neural stem/progenitor cells transplantation |
title | In vivo monitoring of remnant undifferentiated neural cells following human induced pluripotent stem cell‐derived neural stem/progenitor cells transplantation |
title_full | In vivo monitoring of remnant undifferentiated neural cells following human induced pluripotent stem cell‐derived neural stem/progenitor cells transplantation |
title_fullStr | In vivo monitoring of remnant undifferentiated neural cells following human induced pluripotent stem cell‐derived neural stem/progenitor cells transplantation |
title_full_unstemmed | In vivo monitoring of remnant undifferentiated neural cells following human induced pluripotent stem cell‐derived neural stem/progenitor cells transplantation |
title_short | In vivo monitoring of remnant undifferentiated neural cells following human induced pluripotent stem cell‐derived neural stem/progenitor cells transplantation |
title_sort | in vivo monitoring of remnant undifferentiated neural cells following human induced pluripotent stem cell‐derived neural stem/progenitor cells transplantation |
topic | Enabling Technologies for Cell‐based Clinical Translation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7103627/ https://www.ncbi.nlm.nih.gov/pubmed/31904914 http://dx.doi.org/10.1002/sctm.19-0150 |
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