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Generation of embryonic stem cells derived from the inner cell mass of blastocysts of outbred ICR mice

Embryonic stem cells (ESCs) derived from outbred mice which share several genetic characteristics similar to humans have been requested for developing stem cell-based bioengineering techniques directly applicable to humans. Here, we report the generation of ESCs derived from the inner cell mass of b...

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Autores principales: Han, Na Rae, Baek, Song, Kim, Hwa-Young, Lee, Kwon Young, Yun, Jung Im, Choi, Jung Hoon, Lee, Eunsong, Park, Choon-Keun, Lee, Seung Tae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7241472/
https://www.ncbi.nlm.nih.gov/pubmed/32489688
http://dx.doi.org/10.1080/19768354.2020.1752306
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author Han, Na Rae
Baek, Song
Kim, Hwa-Young
Lee, Kwon Young
Yun, Jung Im
Choi, Jung Hoon
Lee, Eunsong
Park, Choon-Keun
Lee, Seung Tae
author_facet Han, Na Rae
Baek, Song
Kim, Hwa-Young
Lee, Kwon Young
Yun, Jung Im
Choi, Jung Hoon
Lee, Eunsong
Park, Choon-Keun
Lee, Seung Tae
author_sort Han, Na Rae
collection PubMed
description Embryonic stem cells (ESCs) derived from outbred mice which share several genetic characteristics similar to humans have been requested for developing stem cell-based bioengineering techniques directly applicable to humans. Here, we report the generation of ESCs derived from the inner cell mass of blastocysts retrieved from 9-week-old female outbred ICR mice mated with 9-week-old male outbred ICR mice ((ICR)ESCs). Similar to those from 129/Ola mouse blastocysts ((E14)ESCs), the established (ICR)ESCs showed inherent characteristics of ESCs except for partial and weak protein expression and activity of alkaline phosphatase. Moreover, (ICR)ESCs were not originated from embryonic germ cells or pluripotent cells that may co-exist in outbred ICR strain-derived mouse embryonic fibroblasts ((ICR)MEFs) used for deriving colonies from inner cell mass of outbred ICR mouse blastocysts. Furthermore, instead of outbred (ICR)MEFs, hybrid (B6CBAF1)MEFs as feeder cells could sufficiently support in vitro maintenance of (ICR)ESC self-renewal. Additionally, (ICR)ESC-specific characteristics (self-renewal, pluripotency, and chromosomal normality) were observed in (ICR)ESCs cultured for 40th subpassages (164 days) on (B6CBAF1)MEFs without any alterations. These results confirmed the successful establishment of ESCs derived from outbred ICR mice, and indicated that self-renewal and pluripotency of the established (ICR)ESCs could be maintained on (B6CBAF1)MEFs in culture.
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spelling pubmed-72414722020-06-01 Generation of embryonic stem cells derived from the inner cell mass of blastocysts of outbred ICR mice Han, Na Rae Baek, Song Kim, Hwa-Young Lee, Kwon Young Yun, Jung Im Choi, Jung Hoon Lee, Eunsong Park, Choon-Keun Lee, Seung Tae Anim Cells Syst (Seoul) Developmental Biology Embryonic stem cells (ESCs) derived from outbred mice which share several genetic characteristics similar to humans have been requested for developing stem cell-based bioengineering techniques directly applicable to humans. Here, we report the generation of ESCs derived from the inner cell mass of blastocysts retrieved from 9-week-old female outbred ICR mice mated with 9-week-old male outbred ICR mice ((ICR)ESCs). Similar to those from 129/Ola mouse blastocysts ((E14)ESCs), the established (ICR)ESCs showed inherent characteristics of ESCs except for partial and weak protein expression and activity of alkaline phosphatase. Moreover, (ICR)ESCs were not originated from embryonic germ cells or pluripotent cells that may co-exist in outbred ICR strain-derived mouse embryonic fibroblasts ((ICR)MEFs) used for deriving colonies from inner cell mass of outbred ICR mouse blastocysts. Furthermore, instead of outbred (ICR)MEFs, hybrid (B6CBAF1)MEFs as feeder cells could sufficiently support in vitro maintenance of (ICR)ESC self-renewal. Additionally, (ICR)ESC-specific characteristics (self-renewal, pluripotency, and chromosomal normality) were observed in (ICR)ESCs cultured for 40th subpassages (164 days) on (B6CBAF1)MEFs without any alterations. These results confirmed the successful establishment of ESCs derived from outbred ICR mice, and indicated that self-renewal and pluripotency of the established (ICR)ESCs could be maintained on (B6CBAF1)MEFs in culture. Taylor & Francis 2020-04-16 /pmc/articles/PMC7241472/ /pubmed/32489688 http://dx.doi.org/10.1080/19768354.2020.1752306 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Developmental Biology
Han, Na Rae
Baek, Song
Kim, Hwa-Young
Lee, Kwon Young
Yun, Jung Im
Choi, Jung Hoon
Lee, Eunsong
Park, Choon-Keun
Lee, Seung Tae
Generation of embryonic stem cells derived from the inner cell mass of blastocysts of outbred ICR mice
title Generation of embryonic stem cells derived from the inner cell mass of blastocysts of outbred ICR mice
title_full Generation of embryonic stem cells derived from the inner cell mass of blastocysts of outbred ICR mice
title_fullStr Generation of embryonic stem cells derived from the inner cell mass of blastocysts of outbred ICR mice
title_full_unstemmed Generation of embryonic stem cells derived from the inner cell mass of blastocysts of outbred ICR mice
title_short Generation of embryonic stem cells derived from the inner cell mass of blastocysts of outbred ICR mice
title_sort generation of embryonic stem cells derived from the inner cell mass of blastocysts of outbred icr mice
topic Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7241472/
https://www.ncbi.nlm.nih.gov/pubmed/32489688
http://dx.doi.org/10.1080/19768354.2020.1752306
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