Cargando…
Human umbilical cord mesenchymal stem cell treatment alleviates symptoms in an atopic dermatitis-like mouse model
BACKGROUND: Atopic dermatitis (AD) is one of the most common immune and inflammatory skin disorders, leading to insufferable itching and skin abnormalities that seriously affect life quality of patients. There are still huge unmet needs for long-term and effective disease control, despite currently...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10227992/ https://www.ncbi.nlm.nih.gov/pubmed/37248497 http://dx.doi.org/10.1186/s13287-023-03365-w |
_version_ | 1785050881206517760 |
---|---|
author | Hua, Chunting Liang, Qichang Chen, Siji Zhu, Jiang Tang, Yi Chen, Xianzhen Song, Yinjing van der Veen, Stijn Cheng, Hao |
author_facet | Hua, Chunting Liang, Qichang Chen, Siji Zhu, Jiang Tang, Yi Chen, Xianzhen Song, Yinjing van der Veen, Stijn Cheng, Hao |
author_sort | Hua, Chunting |
collection | PubMed |
description | BACKGROUND: Atopic dermatitis (AD) is one of the most common immune and inflammatory skin disorders, leading to insufferable itching and skin abnormalities that seriously affect life quality of patients. There are still huge unmet needs for long-term and effective disease control, despite currently available therapies. Evidenced by some preclinical and clinical studies of AD treatment with stem cells, stem cell treatment could significantly and effectively ameliorate AD symptoms. OBJECTIVES: To elucidate underlying mechanisms of how stem cells therapy alleviates AD-like symptoms. METHODS: An AD-like mouse model was constructed and treated with mesenchymal stem cells (MSCs) subcutaneously or subcutaneously combined with intravenously. The differentially expressed genes were sorted out from RNA sequencing results of dorsal skin and blood. RESULTS: Two injection routes of MSCs could alleviate AD-like symptoms and pathologic changes of the skin and immune organs. RNA sequencing of dorsal skin sections and blood provided gene expression signatures for amelioration of skin defects, inflammatory and immune modulation by MSCs, as well as common AD molecular markers for the skin and blood, which may benefit for clinical diagnosis. IL-1β and its signaling pathway were specifically found to be associated with the development of AD-like dermatitis lesions. MSC treatment effectively inhibited the JAK-STAT pathway and receptors of IL-4, IL-13, IL-17, and IgE. CONCLUSIONS: MSC therapy could regulate abnormal immune and inflammatory status in AD. Mechanistic exploration will contribute to the development of personalized AD treatment based on MSCs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-023-03365-w. |
format | Online Article Text |
id | pubmed-10227992 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-102279922023-05-31 Human umbilical cord mesenchymal stem cell treatment alleviates symptoms in an atopic dermatitis-like mouse model Hua, Chunting Liang, Qichang Chen, Siji Zhu, Jiang Tang, Yi Chen, Xianzhen Song, Yinjing van der Veen, Stijn Cheng, Hao Stem Cell Res Ther Research BACKGROUND: Atopic dermatitis (AD) is one of the most common immune and inflammatory skin disorders, leading to insufferable itching and skin abnormalities that seriously affect life quality of patients. There are still huge unmet needs for long-term and effective disease control, despite currently available therapies. Evidenced by some preclinical and clinical studies of AD treatment with stem cells, stem cell treatment could significantly and effectively ameliorate AD symptoms. OBJECTIVES: To elucidate underlying mechanisms of how stem cells therapy alleviates AD-like symptoms. METHODS: An AD-like mouse model was constructed and treated with mesenchymal stem cells (MSCs) subcutaneously or subcutaneously combined with intravenously. The differentially expressed genes were sorted out from RNA sequencing results of dorsal skin and blood. RESULTS: Two injection routes of MSCs could alleviate AD-like symptoms and pathologic changes of the skin and immune organs. RNA sequencing of dorsal skin sections and blood provided gene expression signatures for amelioration of skin defects, inflammatory and immune modulation by MSCs, as well as common AD molecular markers for the skin and blood, which may benefit for clinical diagnosis. IL-1β and its signaling pathway were specifically found to be associated with the development of AD-like dermatitis lesions. MSC treatment effectively inhibited the JAK-STAT pathway and receptors of IL-4, IL-13, IL-17, and IgE. CONCLUSIONS: MSC therapy could regulate abnormal immune and inflammatory status in AD. Mechanistic exploration will contribute to the development of personalized AD treatment based on MSCs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-023-03365-w. BioMed Central 2023-05-29 /pmc/articles/PMC10227992/ /pubmed/37248497 http://dx.doi.org/10.1186/s13287-023-03365-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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 | Research Hua, Chunting Liang, Qichang Chen, Siji Zhu, Jiang Tang, Yi Chen, Xianzhen Song, Yinjing van der Veen, Stijn Cheng, Hao Human umbilical cord mesenchymal stem cell treatment alleviates symptoms in an atopic dermatitis-like mouse model |
title | Human umbilical cord mesenchymal stem cell treatment alleviates symptoms in an atopic dermatitis-like mouse model |
title_full | Human umbilical cord mesenchymal stem cell treatment alleviates symptoms in an atopic dermatitis-like mouse model |
title_fullStr | Human umbilical cord mesenchymal stem cell treatment alleviates symptoms in an atopic dermatitis-like mouse model |
title_full_unstemmed | Human umbilical cord mesenchymal stem cell treatment alleviates symptoms in an atopic dermatitis-like mouse model |
title_short | Human umbilical cord mesenchymal stem cell treatment alleviates symptoms in an atopic dermatitis-like mouse model |
title_sort | human umbilical cord mesenchymal stem cell treatment alleviates symptoms in an atopic dermatitis-like mouse model |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10227992/ https://www.ncbi.nlm.nih.gov/pubmed/37248497 http://dx.doi.org/10.1186/s13287-023-03365-w |
work_keys_str_mv | AT huachunting humanumbilicalcordmesenchymalstemcelltreatmentalleviatessymptomsinanatopicdermatitislikemousemodel AT liangqichang humanumbilicalcordmesenchymalstemcelltreatmentalleviatessymptomsinanatopicdermatitislikemousemodel AT chensiji humanumbilicalcordmesenchymalstemcelltreatmentalleviatessymptomsinanatopicdermatitislikemousemodel AT zhujiang humanumbilicalcordmesenchymalstemcelltreatmentalleviatessymptomsinanatopicdermatitislikemousemodel AT tangyi humanumbilicalcordmesenchymalstemcelltreatmentalleviatessymptomsinanatopicdermatitislikemousemodel AT chenxianzhen humanumbilicalcordmesenchymalstemcelltreatmentalleviatessymptomsinanatopicdermatitislikemousemodel AT songyinjing humanumbilicalcordmesenchymalstemcelltreatmentalleviatessymptomsinanatopicdermatitislikemousemodel AT vanderveenstijn humanumbilicalcordmesenchymalstemcelltreatmentalleviatessymptomsinanatopicdermatitislikemousemodel AT chenghao humanumbilicalcordmesenchymalstemcelltreatmentalleviatessymptomsinanatopicdermatitislikemousemodel |