Cargando…

Inhibition of Epithelial-Mesenchymal Transition Maintains Stemness in Human Amniotic Epithelial Cells

Human amniotic epithelial cells (hAECs), which are a type of placental stem cell, express stem cell marker genes and are capable of differentiating into all three germ layers under appropriate culture conditions. hAECs are known to undergo TGF-β-dependent epithelial-mesenchymal transition (EMT); how...

Descripción completa

Detalles Bibliográficos
Autores principales: Takano, Chika, Horie, Masafumi, Taiko, Isamu, Trinh, Quang Duy, Kanemaru, Kazunori, Komine-Aizawa, Shihoko, Hayakawa, Satoshi, Miki, Toshio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9622541/
https://www.ncbi.nlm.nih.gov/pubmed/35931939
http://dx.doi.org/10.1007/s12015-022-10420-1
_version_ 1784821793215741952
author Takano, Chika
Horie, Masafumi
Taiko, Isamu
Trinh, Quang Duy
Kanemaru, Kazunori
Komine-Aizawa, Shihoko
Hayakawa, Satoshi
Miki, Toshio
author_facet Takano, Chika
Horie, Masafumi
Taiko, Isamu
Trinh, Quang Duy
Kanemaru, Kazunori
Komine-Aizawa, Shihoko
Hayakawa, Satoshi
Miki, Toshio
author_sort Takano, Chika
collection PubMed
description Human amniotic epithelial cells (hAECs), which are a type of placental stem cell, express stem cell marker genes and are capable of differentiating into all three germ layers under appropriate culture conditions. hAECs are known to undergo TGF-β-dependent epithelial-mesenchymal transition (EMT); however, the impact of EMT on the stemness or differentiation of hAECs has not yet been determined. Here, we first confirmed that hAECs undergo EMT immediately after starting primary culture. Comprehensive transcriptome analysis using RNA-seq revealed that inhibition of TGF-β-dependent EMT maintained the expression of stemness-related genes, including NANOG and POU5F1, in hAECs. Moreover, the maintenance of stemness did not affect the nontumorigenic characteristics of hAECs. We showed for the first time that TGF-β-dependent EMT negatively affected the stemness of hAECs, providing novel insight into cellular processes of placental stem cells. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12015-022-10420-1.
format Online
Article
Text
id pubmed-9622541
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Springer US
record_format MEDLINE/PubMed
spelling pubmed-96225412022-11-02 Inhibition of Epithelial-Mesenchymal Transition Maintains Stemness in Human Amniotic Epithelial Cells Takano, Chika Horie, Masafumi Taiko, Isamu Trinh, Quang Duy Kanemaru, Kazunori Komine-Aizawa, Shihoko Hayakawa, Satoshi Miki, Toshio Stem Cell Rev Rep Article Human amniotic epithelial cells (hAECs), which are a type of placental stem cell, express stem cell marker genes and are capable of differentiating into all three germ layers under appropriate culture conditions. hAECs are known to undergo TGF-β-dependent epithelial-mesenchymal transition (EMT); however, the impact of EMT on the stemness or differentiation of hAECs has not yet been determined. Here, we first confirmed that hAECs undergo EMT immediately after starting primary culture. Comprehensive transcriptome analysis using RNA-seq revealed that inhibition of TGF-β-dependent EMT maintained the expression of stemness-related genes, including NANOG and POU5F1, in hAECs. Moreover, the maintenance of stemness did not affect the nontumorigenic characteristics of hAECs. We showed for the first time that TGF-β-dependent EMT negatively affected the stemness of hAECs, providing novel insight into cellular processes of placental stem cells. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12015-022-10420-1. Springer US 2022-08-06 2022 /pmc/articles/PMC9622541/ /pubmed/35931939 http://dx.doi.org/10.1007/s12015-022-10420-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Takano, Chika
Horie, Masafumi
Taiko, Isamu
Trinh, Quang Duy
Kanemaru, Kazunori
Komine-Aizawa, Shihoko
Hayakawa, Satoshi
Miki, Toshio
Inhibition of Epithelial-Mesenchymal Transition Maintains Stemness in Human Amniotic Epithelial Cells
title Inhibition of Epithelial-Mesenchymal Transition Maintains Stemness in Human Amniotic Epithelial Cells
title_full Inhibition of Epithelial-Mesenchymal Transition Maintains Stemness in Human Amniotic Epithelial Cells
title_fullStr Inhibition of Epithelial-Mesenchymal Transition Maintains Stemness in Human Amniotic Epithelial Cells
title_full_unstemmed Inhibition of Epithelial-Mesenchymal Transition Maintains Stemness in Human Amniotic Epithelial Cells
title_short Inhibition of Epithelial-Mesenchymal Transition Maintains Stemness in Human Amniotic Epithelial Cells
title_sort inhibition of epithelial-mesenchymal transition maintains stemness in human amniotic epithelial cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9622541/
https://www.ncbi.nlm.nih.gov/pubmed/35931939
http://dx.doi.org/10.1007/s12015-022-10420-1
work_keys_str_mv AT takanochika inhibitionofepithelialmesenchymaltransitionmaintainsstemnessinhumanamnioticepithelialcells
AT horiemasafumi inhibitionofepithelialmesenchymaltransitionmaintainsstemnessinhumanamnioticepithelialcells
AT taikoisamu inhibitionofepithelialmesenchymaltransitionmaintainsstemnessinhumanamnioticepithelialcells
AT trinhquangduy inhibitionofepithelialmesenchymaltransitionmaintainsstemnessinhumanamnioticepithelialcells
AT kanemarukazunori inhibitionofepithelialmesenchymaltransitionmaintainsstemnessinhumanamnioticepithelialcells
AT komineaizawashihoko inhibitionofepithelialmesenchymaltransitionmaintainsstemnessinhumanamnioticepithelialcells
AT hayakawasatoshi inhibitionofepithelialmesenchymaltransitionmaintainsstemnessinhumanamnioticepithelialcells
AT mikitoshio inhibitionofepithelialmesenchymaltransitionmaintainsstemnessinhumanamnioticepithelialcells