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Induced Pluripotent Stem Cells Reprogrammed with Three Inhibitors Show Accelerated Differentiation Potentials with High Levels of 2-Cell Stage Marker Expression

Although pluripotent stem cells can generate various types of differentiated cells, it is unclear why lineage-committed stem/progenitor cells derived from pluripotent stem cells are decelerated and why the differentiation-resistant propensity of embryonic stem cell (ESC)/induced pluripotent stem cel...

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Autores principales: Nishihara, Koji, Shiga, Takahiro, Nakamura, Eri, Akiyama, Tomohiko, Sasaki, Takashi, Suzuki, Sadafumi, Ko, Minoru S.H., Tada, Norihiro, Okano, Hideyuki, Akamatsu, Wado
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6373546/
https://www.ncbi.nlm.nih.gov/pubmed/30713040
http://dx.doi.org/10.1016/j.stemcr.2018.12.018
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author Nishihara, Koji
Shiga, Takahiro
Nakamura, Eri
Akiyama, Tomohiko
Sasaki, Takashi
Suzuki, Sadafumi
Ko, Minoru S.H.
Tada, Norihiro
Okano, Hideyuki
Akamatsu, Wado
author_facet Nishihara, Koji
Shiga, Takahiro
Nakamura, Eri
Akiyama, Tomohiko
Sasaki, Takashi
Suzuki, Sadafumi
Ko, Minoru S.H.
Tada, Norihiro
Okano, Hideyuki
Akamatsu, Wado
author_sort Nishihara, Koji
collection PubMed
description Although pluripotent stem cells can generate various types of differentiated cells, it is unclear why lineage-committed stem/progenitor cells derived from pluripotent stem cells are decelerated and why the differentiation-resistant propensity of embryonic stem cell (ESC)/induced pluripotent stem cell (iPSC)-derived cells is predominant compared with the in vivo equivalents derived from embryonic/adult tissues. In this study, we demonstrated that iPSCs reprogrammed and maintained with three chemical inhibitors of the fibroblast growth factor 4-mitogen-activated protein kinase cascade and GSK3β (3i) could be differentiated into all three germ layers more efficiently than the iPSCs reprogrammed without the 3i chemicals, even though they were maintained with 3i chemicals once they were reprogrammed. Although the iPSCs reprogrammed with 3i had increased numbers of Zscan4-positive cells, the Zscan4-positive cells among iPSCs that were reprogrammed without 3i did not have an accelerated differentiation ability. These observations suggest that 3i exposure during the reprogramming period determines the accelerated differentiation/maturation potentials of iPSCs that are stably maintained at the distinct state.
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spelling pubmed-63735462019-02-25 Induced Pluripotent Stem Cells Reprogrammed with Three Inhibitors Show Accelerated Differentiation Potentials with High Levels of 2-Cell Stage Marker Expression Nishihara, Koji Shiga, Takahiro Nakamura, Eri Akiyama, Tomohiko Sasaki, Takashi Suzuki, Sadafumi Ko, Minoru S.H. Tada, Norihiro Okano, Hideyuki Akamatsu, Wado Stem Cell Reports Article Although pluripotent stem cells can generate various types of differentiated cells, it is unclear why lineage-committed stem/progenitor cells derived from pluripotent stem cells are decelerated and why the differentiation-resistant propensity of embryonic stem cell (ESC)/induced pluripotent stem cell (iPSC)-derived cells is predominant compared with the in vivo equivalents derived from embryonic/adult tissues. In this study, we demonstrated that iPSCs reprogrammed and maintained with three chemical inhibitors of the fibroblast growth factor 4-mitogen-activated protein kinase cascade and GSK3β (3i) could be differentiated into all three germ layers more efficiently than the iPSCs reprogrammed without the 3i chemicals, even though they were maintained with 3i chemicals once they were reprogrammed. Although the iPSCs reprogrammed with 3i had increased numbers of Zscan4-positive cells, the Zscan4-positive cells among iPSCs that were reprogrammed without 3i did not have an accelerated differentiation ability. These observations suggest that 3i exposure during the reprogramming period determines the accelerated differentiation/maturation potentials of iPSCs that are stably maintained at the distinct state. Elsevier 2019-01-31 /pmc/articles/PMC6373546/ /pubmed/30713040 http://dx.doi.org/10.1016/j.stemcr.2018.12.018 Text en © 2019 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
Nishihara, Koji
Shiga, Takahiro
Nakamura, Eri
Akiyama, Tomohiko
Sasaki, Takashi
Suzuki, Sadafumi
Ko, Minoru S.H.
Tada, Norihiro
Okano, Hideyuki
Akamatsu, Wado
Induced Pluripotent Stem Cells Reprogrammed with Three Inhibitors Show Accelerated Differentiation Potentials with High Levels of 2-Cell Stage Marker Expression
title Induced Pluripotent Stem Cells Reprogrammed with Three Inhibitors Show Accelerated Differentiation Potentials with High Levels of 2-Cell Stage Marker Expression
title_full Induced Pluripotent Stem Cells Reprogrammed with Three Inhibitors Show Accelerated Differentiation Potentials with High Levels of 2-Cell Stage Marker Expression
title_fullStr Induced Pluripotent Stem Cells Reprogrammed with Three Inhibitors Show Accelerated Differentiation Potentials with High Levels of 2-Cell Stage Marker Expression
title_full_unstemmed Induced Pluripotent Stem Cells Reprogrammed with Three Inhibitors Show Accelerated Differentiation Potentials with High Levels of 2-Cell Stage Marker Expression
title_short Induced Pluripotent Stem Cells Reprogrammed with Three Inhibitors Show Accelerated Differentiation Potentials with High Levels of 2-Cell Stage Marker Expression
title_sort induced pluripotent stem cells reprogrammed with three inhibitors show accelerated differentiation potentials with high levels of 2-cell stage marker expression
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6373546/
https://www.ncbi.nlm.nih.gov/pubmed/30713040
http://dx.doi.org/10.1016/j.stemcr.2018.12.018
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