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Sweat gland organoids contribute to cutaneous wound healing and sweat gland regeneration

Sweat glands perform a vital thermoregulatory function in mammals. Like other skin components, they originate from epidermal progenitors. However, they have low regenerative potential in response to injury. We have established a sweat gland culture and expansion method using 3D organoids cultures. T...

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Autores principales: Diao, Jinmei, Liu, Juan, Wang, Shuyong, Chang, Mingyang, Wang, Xuan, Guo, Baolin, Yu, Qunfang, Yan, Fang, Su, Yuxin, Wang, Yunfang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411741/
https://www.ncbi.nlm.nih.gov/pubmed/30858357
http://dx.doi.org/10.1038/s41419-019-1485-5
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author Diao, Jinmei
Liu, Juan
Wang, Shuyong
Chang, Mingyang
Wang, Xuan
Guo, Baolin
Yu, Qunfang
Yan, Fang
Su, Yuxin
Wang, Yunfang
author_facet Diao, Jinmei
Liu, Juan
Wang, Shuyong
Chang, Mingyang
Wang, Xuan
Guo, Baolin
Yu, Qunfang
Yan, Fang
Su, Yuxin
Wang, Yunfang
author_sort Diao, Jinmei
collection PubMed
description Sweat glands perform a vital thermoregulatory function in mammals. Like other skin components, they originate from epidermal progenitors. However, they have low regenerative potential in response to injury. We have established a sweat gland culture and expansion method using 3D organoids cultures. The epithelial cells derived from sweat glands in dermis of adult mouse paw pads were embedded into Matrigel and formed sweat gland organoids (SGOs). These organoids maintained remarkable stem cell features and demonstrated differentiation capacity to give rise to either sweat gland cells (SGCs) or epidermal cells. Moreover, the bipotent SGO-derived cells could be induced into stratified epidermis structures at the air−liquid interface culture in a medium tailored for skin epidermal cells in vitro. The SGCs embedded in Matrigel tailored for sweat glands formed epithelial organoids, which expressed sweat-gland-specific markers, such as cytokeratin (CK) 18 and CK19, aquaporin (AQP) 5 and αATP. More importantly, they had potential of regeneration of epidermis and sweat gland when they were transplanted into the mouse back wound and claw pad with sweat gland injury, respectively. In summary, we established and optimized culture conditions for effective generation of mouse SGOs. These cells are candidates to restore impaired sweat gland tissue as well as to improve cutaneous skin regeneration.
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spelling pubmed-64117412019-03-12 Sweat gland organoids contribute to cutaneous wound healing and sweat gland regeneration Diao, Jinmei Liu, Juan Wang, Shuyong Chang, Mingyang Wang, Xuan Guo, Baolin Yu, Qunfang Yan, Fang Su, Yuxin Wang, Yunfang Cell Death Dis Article Sweat glands perform a vital thermoregulatory function in mammals. Like other skin components, they originate from epidermal progenitors. However, they have low regenerative potential in response to injury. We have established a sweat gland culture and expansion method using 3D organoids cultures. The epithelial cells derived from sweat glands in dermis of adult mouse paw pads were embedded into Matrigel and formed sweat gland organoids (SGOs). These organoids maintained remarkable stem cell features and demonstrated differentiation capacity to give rise to either sweat gland cells (SGCs) or epidermal cells. Moreover, the bipotent SGO-derived cells could be induced into stratified epidermis structures at the air−liquid interface culture in a medium tailored for skin epidermal cells in vitro. The SGCs embedded in Matrigel tailored for sweat glands formed epithelial organoids, which expressed sweat-gland-specific markers, such as cytokeratin (CK) 18 and CK19, aquaporin (AQP) 5 and αATP. More importantly, they had potential of regeneration of epidermis and sweat gland when they were transplanted into the mouse back wound and claw pad with sweat gland injury, respectively. In summary, we established and optimized culture conditions for effective generation of mouse SGOs. These cells are candidates to restore impaired sweat gland tissue as well as to improve cutaneous skin regeneration. Nature Publishing Group UK 2019-03-11 /pmc/articles/PMC6411741/ /pubmed/30858357 http://dx.doi.org/10.1038/s41419-019-1485-5 Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Diao, Jinmei
Liu, Juan
Wang, Shuyong
Chang, Mingyang
Wang, Xuan
Guo, Baolin
Yu, Qunfang
Yan, Fang
Su, Yuxin
Wang, Yunfang
Sweat gland organoids contribute to cutaneous wound healing and sweat gland regeneration
title Sweat gland organoids contribute to cutaneous wound healing and sweat gland regeneration
title_full Sweat gland organoids contribute to cutaneous wound healing and sweat gland regeneration
title_fullStr Sweat gland organoids contribute to cutaneous wound healing and sweat gland regeneration
title_full_unstemmed Sweat gland organoids contribute to cutaneous wound healing and sweat gland regeneration
title_short Sweat gland organoids contribute to cutaneous wound healing and sweat gland regeneration
title_sort sweat gland organoids contribute to cutaneous wound healing and sweat gland regeneration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411741/
https://www.ncbi.nlm.nih.gov/pubmed/30858357
http://dx.doi.org/10.1038/s41419-019-1485-5
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