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Three-dimensional Differentiated Human Mesenchymal Stem Cells Exhibit Robust Antifibrotic Potential and Ameliorates Mouse Liver Fibrosis
Recently, three-dimensional (3D)-cultured adipose mesenchymal stem cells (ASCs) have provided an effective therapy for liver fibrosis. This study aimed to enhance the potential of human ASCs for antifibrosis or hepatocyte regeneration using a 3D culture system and investigate their therapeutic mecha...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7876751/ https://www.ncbi.nlm.nih.gov/pubmed/33555212 http://dx.doi.org/10.1177/0963689720987525 |
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author | Choi, Ja Sung Park, Young-Jin Kim, Sung-Whan |
author_facet | Choi, Ja Sung Park, Young-Jin Kim, Sung-Whan |
author_sort | Choi, Ja Sung |
collection | PubMed |
description | Recently, three-dimensional (3D)-cultured adipose mesenchymal stem cells (ASCs) have provided an effective therapy for liver fibrosis. This study aimed to enhance the potential of human ASCs for antifibrosis or hepatocyte regeneration using a 3D culture system and investigate their therapeutic mechanism in experimental liver fibrosis. ASC-3Dc were generated in a 3D culture system and stimulated with four growth factors, namely epidermal growth factor, insulin-like growth factor (IGF)-1, fibroblast growth factor-2, and vascular endothelial growth factor-A. The expression levels of antifibrotic or hepatic regeneration factors were then measured using quantitative real-time polymerase chain reaction and enzyme-linked immunosorbent assay. The therapeutic effects of ASC-3Dc were determined using a liver fibrosis model induced by thioacetamide. Histological analysis was performed to elucidate the therapeutic mechanism. ASC-3Dc exhibited high levels of hepatocyte growth factor (HGF), IGF-1, stromal cell-derived factor (SDF)-1 genes, and protein expression. In addition, injecting ASC-3Dc significantly prevented hepatic fibrosis and improved liver function in vivo. Moreover, high numbers of ki-67-expressing hepatocytes were detected in the ASC-3Dc-injected livers. Albumin-expressing ASC-3Dc engrafted in fibrotic livers augmented HGF expression. Thus, short-term 3D-cultured ASCs may be a novel alternative to the conventional treatment for liver damage in clinical settings. |
format | Online Article Text |
id | pubmed-7876751 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-78767512021-02-22 Three-dimensional Differentiated Human Mesenchymal Stem Cells Exhibit Robust Antifibrotic Potential and Ameliorates Mouse Liver Fibrosis Choi, Ja Sung Park, Young-Jin Kim, Sung-Whan Cell Transplant Original Article Recently, three-dimensional (3D)-cultured adipose mesenchymal stem cells (ASCs) have provided an effective therapy for liver fibrosis. This study aimed to enhance the potential of human ASCs for antifibrosis or hepatocyte regeneration using a 3D culture system and investigate their therapeutic mechanism in experimental liver fibrosis. ASC-3Dc were generated in a 3D culture system and stimulated with four growth factors, namely epidermal growth factor, insulin-like growth factor (IGF)-1, fibroblast growth factor-2, and vascular endothelial growth factor-A. The expression levels of antifibrotic or hepatic regeneration factors were then measured using quantitative real-time polymerase chain reaction and enzyme-linked immunosorbent assay. The therapeutic effects of ASC-3Dc were determined using a liver fibrosis model induced by thioacetamide. Histological analysis was performed to elucidate the therapeutic mechanism. ASC-3Dc exhibited high levels of hepatocyte growth factor (HGF), IGF-1, stromal cell-derived factor (SDF)-1 genes, and protein expression. In addition, injecting ASC-3Dc significantly prevented hepatic fibrosis and improved liver function in vivo. Moreover, high numbers of ki-67-expressing hepatocytes were detected in the ASC-3Dc-injected livers. Albumin-expressing ASC-3Dc engrafted in fibrotic livers augmented HGF expression. Thus, short-term 3D-cultured ASCs may be a novel alternative to the conventional treatment for liver damage in clinical settings. SAGE Publications 2021-02-08 /pmc/articles/PMC7876751/ /pubmed/33555212 http://dx.doi.org/10.1177/0963689720987525 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Choi, Ja Sung Park, Young-Jin Kim, Sung-Whan Three-dimensional Differentiated Human Mesenchymal Stem Cells Exhibit Robust Antifibrotic Potential and Ameliorates Mouse Liver Fibrosis |
title | Three-dimensional Differentiated Human Mesenchymal Stem Cells Exhibit
Robust Antifibrotic Potential and Ameliorates Mouse Liver
Fibrosis |
title_full | Three-dimensional Differentiated Human Mesenchymal Stem Cells Exhibit
Robust Antifibrotic Potential and Ameliorates Mouse Liver
Fibrosis |
title_fullStr | Three-dimensional Differentiated Human Mesenchymal Stem Cells Exhibit
Robust Antifibrotic Potential and Ameliorates Mouse Liver
Fibrosis |
title_full_unstemmed | Three-dimensional Differentiated Human Mesenchymal Stem Cells Exhibit
Robust Antifibrotic Potential and Ameliorates Mouse Liver
Fibrosis |
title_short | Three-dimensional Differentiated Human Mesenchymal Stem Cells Exhibit
Robust Antifibrotic Potential and Ameliorates Mouse Liver
Fibrosis |
title_sort | three-dimensional differentiated human mesenchymal stem cells exhibit
robust antifibrotic potential and ameliorates mouse liver
fibrosis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7876751/ https://www.ncbi.nlm.nih.gov/pubmed/33555212 http://dx.doi.org/10.1177/0963689720987525 |
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