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Transcriptomic differences between human 8-cell-like cells reprogrammed with different methods

Embryonic genome activation (EGA) is a critical step in embryonic development. However, while EGA has been studied in mice using mouse 2-cell-like cells, human EGA remains incompletely elucidated due to the lack of an in vitro cell model recapitulating the early blastomere stage in humans. Recently,...

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Detalles Bibliográficos
Autores principales: Yoshihara, Masahito, Kere, Juha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10444576/
https://www.ncbi.nlm.nih.gov/pubmed/37478859
http://dx.doi.org/10.1016/j.stemcr.2023.06.009
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author Yoshihara, Masahito
Kere, Juha
author_facet Yoshihara, Masahito
Kere, Juha
author_sort Yoshihara, Masahito
collection PubMed
description Embryonic genome activation (EGA) is a critical step in embryonic development. However, while EGA has been studied in mice using mouse 2-cell-like cells, human EGA remains incompletely elucidated due to the lack of an in vitro cell model recapitulating the early blastomere stage in humans. Recently, five groups independently reported human 8-cell-like cells (8CLCs, also called induced blastomere-like cells) developed from pluripotent stem cells and used single-cell RNA sequencing (scRNA-seq) to specify their cellular identities. Here we summarize the methods developed to produce the 8CLCs and compare their transcriptomic profiles by integrating them with the scRNA-seq datasets of human embryos. These observations will allow comparison and validation of the models, stimulate further in-depth research to characterize the genes involved in human EGA and pre-implantation development, and facilitate studies on human embryogenesis.
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spelling pubmed-104445762023-08-24 Transcriptomic differences between human 8-cell-like cells reprogrammed with different methods Yoshihara, Masahito Kere, Juha Stem Cell Reports Report Embryonic genome activation (EGA) is a critical step in embryonic development. However, while EGA has been studied in mice using mouse 2-cell-like cells, human EGA remains incompletely elucidated due to the lack of an in vitro cell model recapitulating the early blastomere stage in humans. Recently, five groups independently reported human 8-cell-like cells (8CLCs, also called induced blastomere-like cells) developed from pluripotent stem cells and used single-cell RNA sequencing (scRNA-seq) to specify their cellular identities. Here we summarize the methods developed to produce the 8CLCs and compare their transcriptomic profiles by integrating them with the scRNA-seq datasets of human embryos. These observations will allow comparison and validation of the models, stimulate further in-depth research to characterize the genes involved in human EGA and pre-implantation development, and facilitate studies on human embryogenesis. Elsevier 2023-07-20 /pmc/articles/PMC10444576/ /pubmed/37478859 http://dx.doi.org/10.1016/j.stemcr.2023.06.009 Text en © 2023 The Authors https://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 Report
Yoshihara, Masahito
Kere, Juha
Transcriptomic differences between human 8-cell-like cells reprogrammed with different methods
title Transcriptomic differences between human 8-cell-like cells reprogrammed with different methods
title_full Transcriptomic differences between human 8-cell-like cells reprogrammed with different methods
title_fullStr Transcriptomic differences between human 8-cell-like cells reprogrammed with different methods
title_full_unstemmed Transcriptomic differences between human 8-cell-like cells reprogrammed with different methods
title_short Transcriptomic differences between human 8-cell-like cells reprogrammed with different methods
title_sort transcriptomic differences between human 8-cell-like cells reprogrammed with different methods
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10444576/
https://www.ncbi.nlm.nih.gov/pubmed/37478859
http://dx.doi.org/10.1016/j.stemcr.2023.06.009
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