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Transcriptomic and Functional Evidence Show Similarities between Human Amniotic Epithelial Stem Cells and Keratinocytes

Amniotic epithelial stem cells (AESCs) are considered as potential alternatives to keratinocytes (KCs) in tissue-engineered skin substitutes used for treating skin damage. However, their clinical application is limited since similarities and distinctions between AESCs and KCs remain unclear. Herein,...

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Autores principales: Liu, Li-Ping, Zheng, Dong-Xu, Xu, Zheng-Fang, Zhou, Hu-Cheng, Wang, Yun-Cong, Zhou, Hang, Ge, Jian-Yun, Sako, Daisuke, Li, Mi, Akimoto, Kazunori, Li, Yu-Mei, Zheng, Yun-Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8750621/
https://www.ncbi.nlm.nih.gov/pubmed/35011631
http://dx.doi.org/10.3390/cells11010070
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author Liu, Li-Ping
Zheng, Dong-Xu
Xu, Zheng-Fang
Zhou, Hu-Cheng
Wang, Yun-Cong
Zhou, Hang
Ge, Jian-Yun
Sako, Daisuke
Li, Mi
Akimoto, Kazunori
Li, Yu-Mei
Zheng, Yun-Wen
author_facet Liu, Li-Ping
Zheng, Dong-Xu
Xu, Zheng-Fang
Zhou, Hu-Cheng
Wang, Yun-Cong
Zhou, Hang
Ge, Jian-Yun
Sako, Daisuke
Li, Mi
Akimoto, Kazunori
Li, Yu-Mei
Zheng, Yun-Wen
author_sort Liu, Li-Ping
collection PubMed
description Amniotic epithelial stem cells (AESCs) are considered as potential alternatives to keratinocytes (KCs) in tissue-engineered skin substitutes used for treating skin damage. However, their clinical application is limited since similarities and distinctions between AESCs and KCs remain unclear. Herein, a transcriptomics analysis and functional evaluation were used to understand the commonalities and differences between AESCs and KCs. RNA-sequencing revealed that AESCs are involved in multiple epidermis-associated biological processes shared by KCs and show more similarity to early stage immature KCs than to adult KCs. However, AESCs were observed to be heterogeneous, and some possessed hybrid mesenchymal and epithelial features distinct from KCs. A functional evaluation revealed that AESCs can phagocytose melanosomes transported by melanocytes in both 2D and 3D co-culture systems similar to KCs, which may help reconstitute pigmented skin. The overexpression of TP63 and activation of NOTCH signaling could promote AESC stemness and improve their differentiation features, respectively, bridging the gap between AESCs and KCs. These changes induced the convergence of AESC cell fate with KCs. In future, modified reprogramming strategies, such as the use of small molecules, may facilitate the further modulation human AESCs for use in skin regeneration.
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spelling pubmed-87506212022-01-12 Transcriptomic and Functional Evidence Show Similarities between Human Amniotic Epithelial Stem Cells and Keratinocytes Liu, Li-Ping Zheng, Dong-Xu Xu, Zheng-Fang Zhou, Hu-Cheng Wang, Yun-Cong Zhou, Hang Ge, Jian-Yun Sako, Daisuke Li, Mi Akimoto, Kazunori Li, Yu-Mei Zheng, Yun-Wen Cells Article Amniotic epithelial stem cells (AESCs) are considered as potential alternatives to keratinocytes (KCs) in tissue-engineered skin substitutes used for treating skin damage. However, their clinical application is limited since similarities and distinctions between AESCs and KCs remain unclear. Herein, a transcriptomics analysis and functional evaluation were used to understand the commonalities and differences between AESCs and KCs. RNA-sequencing revealed that AESCs are involved in multiple epidermis-associated biological processes shared by KCs and show more similarity to early stage immature KCs than to adult KCs. However, AESCs were observed to be heterogeneous, and some possessed hybrid mesenchymal and epithelial features distinct from KCs. A functional evaluation revealed that AESCs can phagocytose melanosomes transported by melanocytes in both 2D and 3D co-culture systems similar to KCs, which may help reconstitute pigmented skin. The overexpression of TP63 and activation of NOTCH signaling could promote AESC stemness and improve their differentiation features, respectively, bridging the gap between AESCs and KCs. These changes induced the convergence of AESC cell fate with KCs. In future, modified reprogramming strategies, such as the use of small molecules, may facilitate the further modulation human AESCs for use in skin regeneration. MDPI 2021-12-27 /pmc/articles/PMC8750621/ /pubmed/35011631 http://dx.doi.org/10.3390/cells11010070 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Liu, Li-Ping
Zheng, Dong-Xu
Xu, Zheng-Fang
Zhou, Hu-Cheng
Wang, Yun-Cong
Zhou, Hang
Ge, Jian-Yun
Sako, Daisuke
Li, Mi
Akimoto, Kazunori
Li, Yu-Mei
Zheng, Yun-Wen
Transcriptomic and Functional Evidence Show Similarities between Human Amniotic Epithelial Stem Cells and Keratinocytes
title Transcriptomic and Functional Evidence Show Similarities between Human Amniotic Epithelial Stem Cells and Keratinocytes
title_full Transcriptomic and Functional Evidence Show Similarities between Human Amniotic Epithelial Stem Cells and Keratinocytes
title_fullStr Transcriptomic and Functional Evidence Show Similarities between Human Amniotic Epithelial Stem Cells and Keratinocytes
title_full_unstemmed Transcriptomic and Functional Evidence Show Similarities between Human Amniotic Epithelial Stem Cells and Keratinocytes
title_short Transcriptomic and Functional Evidence Show Similarities between Human Amniotic Epithelial Stem Cells and Keratinocytes
title_sort transcriptomic and functional evidence show similarities between human amniotic epithelial stem cells and keratinocytes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8750621/
https://www.ncbi.nlm.nih.gov/pubmed/35011631
http://dx.doi.org/10.3390/cells11010070
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