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Inflammatory cytokines-stimulated human muscle stem cells ameliorate ulcerative colitis via the IDO-TSG6 axis

BACKGROUND: Muscle stem cells (MuSCs) are absolutely required for the formation, repair, and regeneration of skeletal muscle tissue. Increasing evidence demonstrated that tissue stem cells, especially mesenchymal stem cells (MSCs), can exert therapeutic effects on various degenerative and inflammato...

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Autores principales: Zhang, Shengchao, Fang, Jiankai, Liu, Zhanhong, Hou, Pengbo, Cao, Lijuan, Zhang, Yuyan, Liu, Rui, Li, Yanan, Shang, Qianwen, Chen, Yongjing, Feng, Chao, Wang, Guan, Melino, Gerry, Wang, Ying, Shao, Changshun, Shi, Yufang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7796621/
https://www.ncbi.nlm.nih.gov/pubmed/33422134
http://dx.doi.org/10.1186/s13287-020-02118-3
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author Zhang, Shengchao
Fang, Jiankai
Liu, Zhanhong
Hou, Pengbo
Cao, Lijuan
Zhang, Yuyan
Liu, Rui
Li, Yanan
Shang, Qianwen
Chen, Yongjing
Feng, Chao
Wang, Guan
Melino, Gerry
Wang, Ying
Shao, Changshun
Shi, Yufang
author_facet Zhang, Shengchao
Fang, Jiankai
Liu, Zhanhong
Hou, Pengbo
Cao, Lijuan
Zhang, Yuyan
Liu, Rui
Li, Yanan
Shang, Qianwen
Chen, Yongjing
Feng, Chao
Wang, Guan
Melino, Gerry
Wang, Ying
Shao, Changshun
Shi, Yufang
author_sort Zhang, Shengchao
collection PubMed
description BACKGROUND: Muscle stem cells (MuSCs) are absolutely required for the formation, repair, and regeneration of skeletal muscle tissue. Increasing evidence demonstrated that tissue stem cells, especially mesenchymal stem cells (MSCs), can exert therapeutic effects on various degenerative and inflammatory disorders based on their immunoregulatory properties. Human mesenchymal stem cells (hMSCs) treated with interferon-γ (IFN-γ) and tumor necrosis factor-α (TNF-α) were reported to possess anti-inflammatory functions by producing TNF-stimulated gene 6 (TSG-6). However, whether human muscle stem cells (hMuSCs) also possess TSG-6 mediated anti-inflammatory functions has not been explored. METHODS: The ulcerative colitis mouse model was established by subjecting mice to dextran sulfate sodium (DSS) in drinking water for 7 days. hMuSCs were pretreated with IFN-γ and TNF-α for 48 h and were then transplanted intravenously at day 2 of DSS administration. Body weights were monitored daily. Indoleamine 2,3-dioxygenase (IDO) and TSG-6 in hMuSCs were knocked down with short hairpin RNA (shRNA) and small interfering RNA (siRNA), respectively. Colon tissues were collected for length measurement and histopathological examination. The serum level of IL-6 in mice was measured by enzyme-linked immunosorbent assay (ELISA). Real-time PCR and Western blot analysis were performed to evaluate gene expression. RESULTS: hMuSCs treated with inflammatory factors significantly ameliorated inflammatory bowel disease (IBD) symptoms. IDO and TSG-6 were greatly upregulated and required for the beneficial effects of hMuSCs on IBD. Mechanistically, the tryptophan metabolites, kynurenine (KYN) or kynurenic acid (KYNA) produced by IDO, augmented the expression of TSG-6 through activating their common receptor aryl hydrocarbon receptor (AHR). CONCLUSION: Inflammatory cytokines-treated hMuSCs can alleviate DSS-induced colitis through IDO-mediated TSG-6 production. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-020-02118-3.
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spelling pubmed-77966212021-01-11 Inflammatory cytokines-stimulated human muscle stem cells ameliorate ulcerative colitis via the IDO-TSG6 axis Zhang, Shengchao Fang, Jiankai Liu, Zhanhong Hou, Pengbo Cao, Lijuan Zhang, Yuyan Liu, Rui Li, Yanan Shang, Qianwen Chen, Yongjing Feng, Chao Wang, Guan Melino, Gerry Wang, Ying Shao, Changshun Shi, Yufang Stem Cell Res Ther Research BACKGROUND: Muscle stem cells (MuSCs) are absolutely required for the formation, repair, and regeneration of skeletal muscle tissue. Increasing evidence demonstrated that tissue stem cells, especially mesenchymal stem cells (MSCs), can exert therapeutic effects on various degenerative and inflammatory disorders based on their immunoregulatory properties. Human mesenchymal stem cells (hMSCs) treated with interferon-γ (IFN-γ) and tumor necrosis factor-α (TNF-α) were reported to possess anti-inflammatory functions by producing TNF-stimulated gene 6 (TSG-6). However, whether human muscle stem cells (hMuSCs) also possess TSG-6 mediated anti-inflammatory functions has not been explored. METHODS: The ulcerative colitis mouse model was established by subjecting mice to dextran sulfate sodium (DSS) in drinking water for 7 days. hMuSCs were pretreated with IFN-γ and TNF-α for 48 h and were then transplanted intravenously at day 2 of DSS administration. Body weights were monitored daily. Indoleamine 2,3-dioxygenase (IDO) and TSG-6 in hMuSCs were knocked down with short hairpin RNA (shRNA) and small interfering RNA (siRNA), respectively. Colon tissues were collected for length measurement and histopathological examination. The serum level of IL-6 in mice was measured by enzyme-linked immunosorbent assay (ELISA). Real-time PCR and Western blot analysis were performed to evaluate gene expression. RESULTS: hMuSCs treated with inflammatory factors significantly ameliorated inflammatory bowel disease (IBD) symptoms. IDO and TSG-6 were greatly upregulated and required for the beneficial effects of hMuSCs on IBD. Mechanistically, the tryptophan metabolites, kynurenine (KYN) or kynurenic acid (KYNA) produced by IDO, augmented the expression of TSG-6 through activating their common receptor aryl hydrocarbon receptor (AHR). CONCLUSION: Inflammatory cytokines-treated hMuSCs can alleviate DSS-induced colitis through IDO-mediated TSG-6 production. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-020-02118-3. BioMed Central 2021-01-09 /pmc/articles/PMC7796621/ /pubmed/33422134 http://dx.doi.org/10.1186/s13287-020-02118-3 Text en © The Author(s) 2021 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 Research
Zhang, Shengchao
Fang, Jiankai
Liu, Zhanhong
Hou, Pengbo
Cao, Lijuan
Zhang, Yuyan
Liu, Rui
Li, Yanan
Shang, Qianwen
Chen, Yongjing
Feng, Chao
Wang, Guan
Melino, Gerry
Wang, Ying
Shao, Changshun
Shi, Yufang
Inflammatory cytokines-stimulated human muscle stem cells ameliorate ulcerative colitis via the IDO-TSG6 axis
title Inflammatory cytokines-stimulated human muscle stem cells ameliorate ulcerative colitis via the IDO-TSG6 axis
title_full Inflammatory cytokines-stimulated human muscle stem cells ameliorate ulcerative colitis via the IDO-TSG6 axis
title_fullStr Inflammatory cytokines-stimulated human muscle stem cells ameliorate ulcerative colitis via the IDO-TSG6 axis
title_full_unstemmed Inflammatory cytokines-stimulated human muscle stem cells ameliorate ulcerative colitis via the IDO-TSG6 axis
title_short Inflammatory cytokines-stimulated human muscle stem cells ameliorate ulcerative colitis via the IDO-TSG6 axis
title_sort inflammatory cytokines-stimulated human muscle stem cells ameliorate ulcerative colitis via the ido-tsg6 axis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7796621/
https://www.ncbi.nlm.nih.gov/pubmed/33422134
http://dx.doi.org/10.1186/s13287-020-02118-3
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