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Promoting Effect of Basic Fibroblast Growth Factor in Synovial Mesenchymal Stem Cell-Based Cartilage Regeneration

Synovial mesenchymal stem cell (SMSC) is the promising cell source of cartilage regeneration but has several issues to overcome such as limited cell proliferation and heterogeneity of cartilage regeneration ability. Previous reports demonstrated that basic fibroblast growth factor (bFGF) can promote...

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Autores principales: Okamura, Gensuke, Ebina, Kosuke, Hirao, Makoto, Chijimatsu, Ryota, Yonetani, Yasukazu, Etani, Yuki, Miyama, Akira, Takami, Kenji, Goshima, Atsushi, Yoshikawa, Hideki, Ishimoto, Takuya, Nakano, Takayoshi, Hamada, Masayuki, Kanamoto, Takashi, Nakata, Ken
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7796036/
https://www.ncbi.nlm.nih.gov/pubmed/33396695
http://dx.doi.org/10.3390/ijms22010300
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author Okamura, Gensuke
Ebina, Kosuke
Hirao, Makoto
Chijimatsu, Ryota
Yonetani, Yasukazu
Etani, Yuki
Miyama, Akira
Takami, Kenji
Goshima, Atsushi
Yoshikawa, Hideki
Ishimoto, Takuya
Nakano, Takayoshi
Hamada, Masayuki
Kanamoto, Takashi
Nakata, Ken
author_facet Okamura, Gensuke
Ebina, Kosuke
Hirao, Makoto
Chijimatsu, Ryota
Yonetani, Yasukazu
Etani, Yuki
Miyama, Akira
Takami, Kenji
Goshima, Atsushi
Yoshikawa, Hideki
Ishimoto, Takuya
Nakano, Takayoshi
Hamada, Masayuki
Kanamoto, Takashi
Nakata, Ken
author_sort Okamura, Gensuke
collection PubMed
description Synovial mesenchymal stem cell (SMSC) is the promising cell source of cartilage regeneration but has several issues to overcome such as limited cell proliferation and heterogeneity of cartilage regeneration ability. Previous reports demonstrated that basic fibroblast growth factor (bFGF) can promote proliferation and cartilage differentiation potential of MSCs in vitro, although no reports show its beneficial effect in vivo. The purpose of this study is to investigate the promoting effect of bFGF on cartilage regeneration using human SMSC in vivo. SMSCs were cultured with or without bFGF in a growth medium, and 2 × 10(5) cells were aggregated to form a synovial pellet. Synovial pellets were implanted into osteochondral defects induced in the femoral trochlea of severe combined immunodeficient mice, and histological evaluation was performed after eight weeks. The presence of implanted SMSCs was confirmed by the observation of human vimentin immunostaining-positive cells. Interestingly, broad lacunae structures and cartilage substrate stained by Safranin-O were observed only in the bFGF (+) group. The bFGF (+) group had significantly higher O’Driscoll scores in the cartilage repair than the bFGF (−) group. The addition of bFGF to SMSC growth culture may be a useful treatment option to promote cartilage regeneration in vivo.
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spelling pubmed-77960362021-01-10 Promoting Effect of Basic Fibroblast Growth Factor in Synovial Mesenchymal Stem Cell-Based Cartilage Regeneration Okamura, Gensuke Ebina, Kosuke Hirao, Makoto Chijimatsu, Ryota Yonetani, Yasukazu Etani, Yuki Miyama, Akira Takami, Kenji Goshima, Atsushi Yoshikawa, Hideki Ishimoto, Takuya Nakano, Takayoshi Hamada, Masayuki Kanamoto, Takashi Nakata, Ken Int J Mol Sci Article Synovial mesenchymal stem cell (SMSC) is the promising cell source of cartilage regeneration but has several issues to overcome such as limited cell proliferation and heterogeneity of cartilage regeneration ability. Previous reports demonstrated that basic fibroblast growth factor (bFGF) can promote proliferation and cartilage differentiation potential of MSCs in vitro, although no reports show its beneficial effect in vivo. The purpose of this study is to investigate the promoting effect of bFGF on cartilage regeneration using human SMSC in vivo. SMSCs were cultured with or without bFGF in a growth medium, and 2 × 10(5) cells were aggregated to form a synovial pellet. Synovial pellets were implanted into osteochondral defects induced in the femoral trochlea of severe combined immunodeficient mice, and histological evaluation was performed after eight weeks. The presence of implanted SMSCs was confirmed by the observation of human vimentin immunostaining-positive cells. Interestingly, broad lacunae structures and cartilage substrate stained by Safranin-O were observed only in the bFGF (+) group. The bFGF (+) group had significantly higher O’Driscoll scores in the cartilage repair than the bFGF (−) group. The addition of bFGF to SMSC growth culture may be a useful treatment option to promote cartilage regeneration in vivo. MDPI 2020-12-30 /pmc/articles/PMC7796036/ /pubmed/33396695 http://dx.doi.org/10.3390/ijms22010300 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Okamura, Gensuke
Ebina, Kosuke
Hirao, Makoto
Chijimatsu, Ryota
Yonetani, Yasukazu
Etani, Yuki
Miyama, Akira
Takami, Kenji
Goshima, Atsushi
Yoshikawa, Hideki
Ishimoto, Takuya
Nakano, Takayoshi
Hamada, Masayuki
Kanamoto, Takashi
Nakata, Ken
Promoting Effect of Basic Fibroblast Growth Factor in Synovial Mesenchymal Stem Cell-Based Cartilage Regeneration
title Promoting Effect of Basic Fibroblast Growth Factor in Synovial Mesenchymal Stem Cell-Based Cartilage Regeneration
title_full Promoting Effect of Basic Fibroblast Growth Factor in Synovial Mesenchymal Stem Cell-Based Cartilage Regeneration
title_fullStr Promoting Effect of Basic Fibroblast Growth Factor in Synovial Mesenchymal Stem Cell-Based Cartilage Regeneration
title_full_unstemmed Promoting Effect of Basic Fibroblast Growth Factor in Synovial Mesenchymal Stem Cell-Based Cartilage Regeneration
title_short Promoting Effect of Basic Fibroblast Growth Factor in Synovial Mesenchymal Stem Cell-Based Cartilage Regeneration
title_sort promoting effect of basic fibroblast growth factor in synovial mesenchymal stem cell-based cartilage regeneration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7796036/
https://www.ncbi.nlm.nih.gov/pubmed/33396695
http://dx.doi.org/10.3390/ijms22010300
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