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Establishment of Induced Pluripotent Stem Cells from Centenarians for Neurodegenerative Disease Research

Induced pluripotent stem cell (iPSC) technology can be used to model human disorders, create cell-based models of human diseases, including neurodegenerative diseases, and in establishing therapeutic strategies. To detect subtle cellular abnormalities associated with common late-onset disease in iPS...

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Detalles Bibliográficos
Autores principales: Yagi, Takuya, Kosakai, Arifumi, Ito, Daisuke, Okada, Yohei, Akamatsu, Wado, Nihei, Yoshihiro, Nabetani, Akira, Ishikawa, Fuyuki, Arai, Yasumichi, Hirose, Nobuyoshi, Okano, Hideyuki, Suzuki, Norihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3405135/
https://www.ncbi.nlm.nih.gov/pubmed/22848530
http://dx.doi.org/10.1371/journal.pone.0041572
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author Yagi, Takuya
Kosakai, Arifumi
Ito, Daisuke
Okada, Yohei
Akamatsu, Wado
Nihei, Yoshihiro
Nabetani, Akira
Ishikawa, Fuyuki
Arai, Yasumichi
Hirose, Nobuyoshi
Okano, Hideyuki
Suzuki, Norihiro
author_facet Yagi, Takuya
Kosakai, Arifumi
Ito, Daisuke
Okada, Yohei
Akamatsu, Wado
Nihei, Yoshihiro
Nabetani, Akira
Ishikawa, Fuyuki
Arai, Yasumichi
Hirose, Nobuyoshi
Okano, Hideyuki
Suzuki, Norihiro
author_sort Yagi, Takuya
collection PubMed
description Induced pluripotent stem cell (iPSC) technology can be used to model human disorders, create cell-based models of human diseases, including neurodegenerative diseases, and in establishing therapeutic strategies. To detect subtle cellular abnormalities associated with common late-onset disease in iPSCs, valid control iPSCs derived from healthy donors free of serious late-onset diseases are necessary. Here, we report the generation of iPSCs from fibroblasts obtained immediately postmortem from centenarian donors (106- and 109-years-old) who were extremely healthy until an advanced age. The iPSCs were generated using a conventional method involving OCT4, SOX2, KLF4, and c-MYC, and then differentiated into neuronal cells using a neurosphere method. The expression of molecules that play critical roles in late-onset neurodegenerative diseases by neurons differentiated from the centenarian-iPSCs was compared to that of neurons differentiated from iPSCs derived from familial Alzheimer's disease and familial Parkinson's disease (PARK4: triplication of the α synuclein gene) patients. The results indicated that our series of iPSCs would be useful in neurodegeneration research. The iPSCs we describe, which were derived from donors with exceptional longevity who were presumed to have no serious disease risk factors, would be useful in longevity research and as valid super-controls for use in studies of various late-onset diseases.
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spelling pubmed-34051352012-07-30 Establishment of Induced Pluripotent Stem Cells from Centenarians for Neurodegenerative Disease Research Yagi, Takuya Kosakai, Arifumi Ito, Daisuke Okada, Yohei Akamatsu, Wado Nihei, Yoshihiro Nabetani, Akira Ishikawa, Fuyuki Arai, Yasumichi Hirose, Nobuyoshi Okano, Hideyuki Suzuki, Norihiro PLoS One Research Article Induced pluripotent stem cell (iPSC) technology can be used to model human disorders, create cell-based models of human diseases, including neurodegenerative diseases, and in establishing therapeutic strategies. To detect subtle cellular abnormalities associated with common late-onset disease in iPSCs, valid control iPSCs derived from healthy donors free of serious late-onset diseases are necessary. Here, we report the generation of iPSCs from fibroblasts obtained immediately postmortem from centenarian donors (106- and 109-years-old) who were extremely healthy until an advanced age. The iPSCs were generated using a conventional method involving OCT4, SOX2, KLF4, and c-MYC, and then differentiated into neuronal cells using a neurosphere method. The expression of molecules that play critical roles in late-onset neurodegenerative diseases by neurons differentiated from the centenarian-iPSCs was compared to that of neurons differentiated from iPSCs derived from familial Alzheimer's disease and familial Parkinson's disease (PARK4: triplication of the α synuclein gene) patients. The results indicated that our series of iPSCs would be useful in neurodegeneration research. The iPSCs we describe, which were derived from donors with exceptional longevity who were presumed to have no serious disease risk factors, would be useful in longevity research and as valid super-controls for use in studies of various late-onset diseases. Public Library of Science 2012-07-25 /pmc/articles/PMC3405135/ /pubmed/22848530 http://dx.doi.org/10.1371/journal.pone.0041572 Text en Yagi et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Yagi, Takuya
Kosakai, Arifumi
Ito, Daisuke
Okada, Yohei
Akamatsu, Wado
Nihei, Yoshihiro
Nabetani, Akira
Ishikawa, Fuyuki
Arai, Yasumichi
Hirose, Nobuyoshi
Okano, Hideyuki
Suzuki, Norihiro
Establishment of Induced Pluripotent Stem Cells from Centenarians for Neurodegenerative Disease Research
title Establishment of Induced Pluripotent Stem Cells from Centenarians for Neurodegenerative Disease Research
title_full Establishment of Induced Pluripotent Stem Cells from Centenarians for Neurodegenerative Disease Research
title_fullStr Establishment of Induced Pluripotent Stem Cells from Centenarians for Neurodegenerative Disease Research
title_full_unstemmed Establishment of Induced Pluripotent Stem Cells from Centenarians for Neurodegenerative Disease Research
title_short Establishment of Induced Pluripotent Stem Cells from Centenarians for Neurodegenerative Disease Research
title_sort establishment of induced pluripotent stem cells from centenarians for neurodegenerative disease research
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3405135/
https://www.ncbi.nlm.nih.gov/pubmed/22848530
http://dx.doi.org/10.1371/journal.pone.0041572
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