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PI3K/Akt signaling pathway is essential for de novo hair follicle regeneration

BACKGROUND: Cultured epidermal stem cells (Epi-SCs) and skin-derived precursors (SKPs) were capable of reconstituting functional hair follicles after implantation, while the signaling pathways that regulate neogenic hair follicle formation are poorly investigated. In this study, we aimed to understa...

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Autores principales: Chen, Yu, Fan, Zhimeng, Wang, Xiaoxiao, Mo, Miaohua, Zeng, Shu Bin, Xu, Ren-He, Wang, Xusheng, Wu, Yaojiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7118821/
https://www.ncbi.nlm.nih.gov/pubmed/32245516
http://dx.doi.org/10.1186/s13287-020-01650-6
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author Chen, Yu
Fan, Zhimeng
Wang, Xiaoxiao
Mo, Miaohua
Zeng, Shu Bin
Xu, Ren-He
Wang, Xusheng
Wu, Yaojiong
author_facet Chen, Yu
Fan, Zhimeng
Wang, Xiaoxiao
Mo, Miaohua
Zeng, Shu Bin
Xu, Ren-He
Wang, Xusheng
Wu, Yaojiong
author_sort Chen, Yu
collection PubMed
description BACKGROUND: Cultured epidermal stem cells (Epi-SCs) and skin-derived precursors (SKPs) were capable of reconstituting functional hair follicles after implantation, while the signaling pathways that regulate neogenic hair follicle formation are poorly investigated. In this study, we aimed to understand the interactions between Epi-SCs and SKPs during skin organoid formation and to uncover key signal pathways crucial for de novo hair follicle regeneration. METHODS: To track their fate after transplantation, Epi-SCs derived from neonatal C57BL/6 mice were labeled with tdTomato, and SKPs were isolated from neonatal C57BL/6/GFP mice. A mixture of Epi-SCs-tdTomato and SKPs-EGFP in Matrigel was observed under two-photon microscope in culture and after implantation into excisional wounds in nude mice, to observe dynamic migrations of the cells during hair follicle morphogenesis. Signaling communications between the two cell populations were examined by RNA-Seq analysis. Potential signaling pathways revealed by the analysis were validated by targeting the pathways using specific inhibitors to observe a functional loss in de novo hair follicle formation. RESULTS: Two-photon microscopy analysis indicated that when Epi-SCs and SKPs were mixed in Matrigel and cultured, they underwent dynamic migrations resulting in the formation of a bilayer skin-like structure (skin organoid), where Epi-SCs positioned themselves in the outer layer; when the mixture of Epi-SCs and SKPs was grafted into excisional wounds in nude mice, a bilayer structure resembling the epidermis and the dermis formed at the 5th day, and de novo hair follicles generated subsequently. RNA-Seq analysis of the two cell types after incubation in mixture revealed dramatic alterations in gene transcriptome, where PI3K-Akt signaling pathway in Epi-SCs was significantly upregulated; meanwhile, elevated expressions of several growth factors and cytokine potentially activating PI3K were found in SKPs, suggesting active reciprocal communications between them. In addition, inhibition of PI3K or Akt by specific inhibitors markedly suppressed the hair follicle regeneration mediated by Epi-SCs and SKPs. CONCLUSIONS: Our data indicate that the PI3K-Akt signaling pathway plays a crucial role in de novo hair follicle regeneration, and the finding may suggest potential therapeutic applications in enhancing hair regeneration.
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spelling pubmed-71188212020-04-07 PI3K/Akt signaling pathway is essential for de novo hair follicle regeneration Chen, Yu Fan, Zhimeng Wang, Xiaoxiao Mo, Miaohua Zeng, Shu Bin Xu, Ren-He Wang, Xusheng Wu, Yaojiong Stem Cell Res Ther Short Report BACKGROUND: Cultured epidermal stem cells (Epi-SCs) and skin-derived precursors (SKPs) were capable of reconstituting functional hair follicles after implantation, while the signaling pathways that regulate neogenic hair follicle formation are poorly investigated. In this study, we aimed to understand the interactions between Epi-SCs and SKPs during skin organoid formation and to uncover key signal pathways crucial for de novo hair follicle regeneration. METHODS: To track their fate after transplantation, Epi-SCs derived from neonatal C57BL/6 mice were labeled with tdTomato, and SKPs were isolated from neonatal C57BL/6/GFP mice. A mixture of Epi-SCs-tdTomato and SKPs-EGFP in Matrigel was observed under two-photon microscope in culture and after implantation into excisional wounds in nude mice, to observe dynamic migrations of the cells during hair follicle morphogenesis. Signaling communications between the two cell populations were examined by RNA-Seq analysis. Potential signaling pathways revealed by the analysis were validated by targeting the pathways using specific inhibitors to observe a functional loss in de novo hair follicle formation. RESULTS: Two-photon microscopy analysis indicated that when Epi-SCs and SKPs were mixed in Matrigel and cultured, they underwent dynamic migrations resulting in the formation of a bilayer skin-like structure (skin organoid), where Epi-SCs positioned themselves in the outer layer; when the mixture of Epi-SCs and SKPs was grafted into excisional wounds in nude mice, a bilayer structure resembling the epidermis and the dermis formed at the 5th day, and de novo hair follicles generated subsequently. RNA-Seq analysis of the two cell types after incubation in mixture revealed dramatic alterations in gene transcriptome, where PI3K-Akt signaling pathway in Epi-SCs was significantly upregulated; meanwhile, elevated expressions of several growth factors and cytokine potentially activating PI3K were found in SKPs, suggesting active reciprocal communications between them. In addition, inhibition of PI3K or Akt by specific inhibitors markedly suppressed the hair follicle regeneration mediated by Epi-SCs and SKPs. CONCLUSIONS: Our data indicate that the PI3K-Akt signaling pathway plays a crucial role in de novo hair follicle regeneration, and the finding may suggest potential therapeutic applications in enhancing hair regeneration. BioMed Central 2020-04-03 /pmc/articles/PMC7118821/ /pubmed/32245516 http://dx.doi.org/10.1186/s13287-020-01650-6 Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Short Report
Chen, Yu
Fan, Zhimeng
Wang, Xiaoxiao
Mo, Miaohua
Zeng, Shu Bin
Xu, Ren-He
Wang, Xusheng
Wu, Yaojiong
PI3K/Akt signaling pathway is essential for de novo hair follicle regeneration
title PI3K/Akt signaling pathway is essential for de novo hair follicle regeneration
title_full PI3K/Akt signaling pathway is essential for de novo hair follicle regeneration
title_fullStr PI3K/Akt signaling pathway is essential for de novo hair follicle regeneration
title_full_unstemmed PI3K/Akt signaling pathway is essential for de novo hair follicle regeneration
title_short PI3K/Akt signaling pathway is essential for de novo hair follicle regeneration
title_sort pi3k/akt signaling pathway is essential for de novo hair follicle regeneration
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7118821/
https://www.ncbi.nlm.nih.gov/pubmed/32245516
http://dx.doi.org/10.1186/s13287-020-01650-6
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