Cargando…
Human Astrocytes Model Derived from Induced Pluripotent Stem Cells
Induced pluripotent stem cell (iPSC)-based disease modeling has a great potential for uncovering the mechanisms of pathogenesis, especially in the case of neurodegenerative diseases where disease-susceptible cells can usually not be obtained from patients. So far, the iPSC-based modeling of neurodeg...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7763297/ https://www.ncbi.nlm.nih.gov/pubmed/33322219 http://dx.doi.org/10.3390/cells9122680 |
_version_ | 1783627985119608832 |
---|---|
author | Leventoux, Nicolas Morimoto, Satoru Imaizumi, Kent Sato, Yuta Takahashi, Shinichi Mashima, Kyoko Ishikawa, Mitsuru Sonn, Iki Kondo, Takahiro Watanabe, Hirotaka Okano, Hideyuki |
author_facet | Leventoux, Nicolas Morimoto, Satoru Imaizumi, Kent Sato, Yuta Takahashi, Shinichi Mashima, Kyoko Ishikawa, Mitsuru Sonn, Iki Kondo, Takahiro Watanabe, Hirotaka Okano, Hideyuki |
author_sort | Leventoux, Nicolas |
collection | PubMed |
description | Induced pluripotent stem cell (iPSC)-based disease modeling has a great potential for uncovering the mechanisms of pathogenesis, especially in the case of neurodegenerative diseases where disease-susceptible cells can usually not be obtained from patients. So far, the iPSC-based modeling of neurodegenerative diseases has mainly focused on neurons because the protocols for generating astrocytes from iPSCs have not been fully established. The growing evidence of astrocytes’ contribution to neurodegenerative diseases has underscored the lack of iPSC-derived astrocyte models. In the present study, we established a protocol to efficiently generate iPSC-derived astrocytes (iPasts), which were further characterized by RNA and protein expression profiles as well as functional assays. iPasts exhibited calcium dynamics and glutamate uptake activity comparable to human primary astrocytes. Moreover, when co-cultured with neurons, iPasts enhanced neuronal synaptic maturation. Our protocol can be used for modeling astrocyte-related disease phenotypes in vitro and further exploring the contribution of astrocytes to neurodegenerative diseases. |
format | Online Article Text |
id | pubmed-7763297 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77632972020-12-27 Human Astrocytes Model Derived from Induced Pluripotent Stem Cells Leventoux, Nicolas Morimoto, Satoru Imaizumi, Kent Sato, Yuta Takahashi, Shinichi Mashima, Kyoko Ishikawa, Mitsuru Sonn, Iki Kondo, Takahiro Watanabe, Hirotaka Okano, Hideyuki Cells Article Induced pluripotent stem cell (iPSC)-based disease modeling has a great potential for uncovering the mechanisms of pathogenesis, especially in the case of neurodegenerative diseases where disease-susceptible cells can usually not be obtained from patients. So far, the iPSC-based modeling of neurodegenerative diseases has mainly focused on neurons because the protocols for generating astrocytes from iPSCs have not been fully established. The growing evidence of astrocytes’ contribution to neurodegenerative diseases has underscored the lack of iPSC-derived astrocyte models. In the present study, we established a protocol to efficiently generate iPSC-derived astrocytes (iPasts), which were further characterized by RNA and protein expression profiles as well as functional assays. iPasts exhibited calcium dynamics and glutamate uptake activity comparable to human primary astrocytes. Moreover, when co-cultured with neurons, iPasts enhanced neuronal synaptic maturation. Our protocol can be used for modeling astrocyte-related disease phenotypes in vitro and further exploring the contribution of astrocytes to neurodegenerative diseases. MDPI 2020-12-13 /pmc/articles/PMC7763297/ /pubmed/33322219 http://dx.doi.org/10.3390/cells9122680 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Leventoux, Nicolas Morimoto, Satoru Imaizumi, Kent Sato, Yuta Takahashi, Shinichi Mashima, Kyoko Ishikawa, Mitsuru Sonn, Iki Kondo, Takahiro Watanabe, Hirotaka Okano, Hideyuki Human Astrocytes Model Derived from Induced Pluripotent Stem Cells |
title | Human Astrocytes Model Derived from Induced Pluripotent Stem Cells |
title_full | Human Astrocytes Model Derived from Induced Pluripotent Stem Cells |
title_fullStr | Human Astrocytes Model Derived from Induced Pluripotent Stem Cells |
title_full_unstemmed | Human Astrocytes Model Derived from Induced Pluripotent Stem Cells |
title_short | Human Astrocytes Model Derived from Induced Pluripotent Stem Cells |
title_sort | human astrocytes model derived from induced pluripotent stem cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7763297/ https://www.ncbi.nlm.nih.gov/pubmed/33322219 http://dx.doi.org/10.3390/cells9122680 |
work_keys_str_mv | AT leventouxnicolas humanastrocytesmodelderivedfrominducedpluripotentstemcells AT morimotosatoru humanastrocytesmodelderivedfrominducedpluripotentstemcells AT imaizumikent humanastrocytesmodelderivedfrominducedpluripotentstemcells AT satoyuta humanastrocytesmodelderivedfrominducedpluripotentstemcells AT takahashishinichi humanastrocytesmodelderivedfrominducedpluripotentstemcells AT mashimakyoko humanastrocytesmodelderivedfrominducedpluripotentstemcells AT ishikawamitsuru humanastrocytesmodelderivedfrominducedpluripotentstemcells AT sonniki humanastrocytesmodelderivedfrominducedpluripotentstemcells AT kondotakahiro humanastrocytesmodelderivedfrominducedpluripotentstemcells AT watanabehirotaka humanastrocytesmodelderivedfrominducedpluripotentstemcells AT okanohideyuki humanastrocytesmodelderivedfrominducedpluripotentstemcells |