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TNFAIP6 defines the MSC subpopulation with enhanced immune suppression activities
BACKGROUND: Mesenchymal stromal/stem cells (MSCs) have been intensively investigated in both pre-clinical and clinical studies. However, the therapeutic efficacy varies resulting from the heterogenicity of MSCs. Therefore, purifying the specific MSC subpopulation with specialized function is necessa...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9509641/ https://www.ncbi.nlm.nih.gov/pubmed/36153571 http://dx.doi.org/10.1186/s13287-022-03176-5 |
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author | Li, Lingyun Yang, Lei Chen, Xian Chen, Xiangjuan Diao, Lianghui Zeng, Yong Xu, Jianyong |
author_facet | Li, Lingyun Yang, Lei Chen, Xian Chen, Xiangjuan Diao, Lianghui Zeng, Yong Xu, Jianyong |
author_sort | Li, Lingyun |
collection | PubMed |
description | BACKGROUND: Mesenchymal stromal/stem cells (MSCs) have been intensively investigated in both pre-clinical and clinical studies. However, the therapeutic efficacy varies resulting from the heterogenicity of MSCs. Therefore, purifying the specific MSC subpopulation with specialized function is necessary for their therapeutic applications. METHODS: The large-scale RNA sequencing analysis was performed to identify potential cell markers for the mouse MSCs. Then, the immune suppression activities of the purified MSC subpopulation were assessed in vitro and in vivo. RESULTS: The TNFAIP6 (tumor necrosis factor alpha-induced protein 6) has been identified as a potential cell marker for mouse MSCs, irrespective of tissue origin and laboratory origin. The TNFAIP6(+) mouse MSCs showed enhanced immune suppression activities and improved therapeutic effects on the mouse model of acute inflammation, resulting from faster response to immune stimulation. CONCLUSIONS: Therefore, we have demonstrated that the TNFAIP6(+) MSC subpopulation has enhanced immune suppression capabilities. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-022-03176-5. |
format | Online Article Text |
id | pubmed-9509641 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-95096412022-09-26 TNFAIP6 defines the MSC subpopulation with enhanced immune suppression activities Li, Lingyun Yang, Lei Chen, Xian Chen, Xiangjuan Diao, Lianghui Zeng, Yong Xu, Jianyong Stem Cell Res Ther Research BACKGROUND: Mesenchymal stromal/stem cells (MSCs) have been intensively investigated in both pre-clinical and clinical studies. However, the therapeutic efficacy varies resulting from the heterogenicity of MSCs. Therefore, purifying the specific MSC subpopulation with specialized function is necessary for their therapeutic applications. METHODS: The large-scale RNA sequencing analysis was performed to identify potential cell markers for the mouse MSCs. Then, the immune suppression activities of the purified MSC subpopulation were assessed in vitro and in vivo. RESULTS: The TNFAIP6 (tumor necrosis factor alpha-induced protein 6) has been identified as a potential cell marker for mouse MSCs, irrespective of tissue origin and laboratory origin. The TNFAIP6(+) mouse MSCs showed enhanced immune suppression activities and improved therapeutic effects on the mouse model of acute inflammation, resulting from faster response to immune stimulation. CONCLUSIONS: Therefore, we have demonstrated that the TNFAIP6(+) MSC subpopulation has enhanced immune suppression capabilities. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-022-03176-5. BioMed Central 2022-09-24 /pmc/articles/PMC9509641/ /pubmed/36153571 http://dx.doi.org/10.1186/s13287-022-03176-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (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 Li, Lingyun Yang, Lei Chen, Xian Chen, Xiangjuan Diao, Lianghui Zeng, Yong Xu, Jianyong TNFAIP6 defines the MSC subpopulation with enhanced immune suppression activities |
title | TNFAIP6 defines the MSC subpopulation with enhanced immune suppression activities |
title_full | TNFAIP6 defines the MSC subpopulation with enhanced immune suppression activities |
title_fullStr | TNFAIP6 defines the MSC subpopulation with enhanced immune suppression activities |
title_full_unstemmed | TNFAIP6 defines the MSC subpopulation with enhanced immune suppression activities |
title_short | TNFAIP6 defines the MSC subpopulation with enhanced immune suppression activities |
title_sort | tnfaip6 defines the msc subpopulation with enhanced immune suppression activities |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9509641/ https://www.ncbi.nlm.nih.gov/pubmed/36153571 http://dx.doi.org/10.1186/s13287-022-03176-5 |
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