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Regenerative effects of human chondrocyte sheets in a xenogeneic transplantation model using immune‐deficient rats

Although cell transplantation has attracted much attention in regenerative medicine, animal models continue to be used in translational research to evaluate safety and efficacy because cell sources and transplantation modalities are so diverse. In the present study, we investigated the regenerative...

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Autores principales: Takizawa, Daichi, Sato, Masato, Okada, Eri, Takahashi, Takumi, Maehara, Miki, Tominaga, Ayako, Sogo, Yasuyuki, Toyoda, Eriko, Watanabe, Masahiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7540669/
https://www.ncbi.nlm.nih.gov/pubmed/32652894
http://dx.doi.org/10.1002/term.3101
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author Takizawa, Daichi
Sato, Masato
Okada, Eri
Takahashi, Takumi
Maehara, Miki
Tominaga, Ayako
Sogo, Yasuyuki
Toyoda, Eriko
Watanabe, Masahiko
author_facet Takizawa, Daichi
Sato, Masato
Okada, Eri
Takahashi, Takumi
Maehara, Miki
Tominaga, Ayako
Sogo, Yasuyuki
Toyoda, Eriko
Watanabe, Masahiko
author_sort Takizawa, Daichi
collection PubMed
description Although cell transplantation has attracted much attention in regenerative medicine, animal models continue to be used in translational research to evaluate safety and efficacy because cell sources and transplantation modalities are so diverse. In the present study, we investigated the regenerative effects of human chondrocyte sheets on articular cartilage in a xenogeneic transplantation model using immune‐deficient rats. Osteochondral defects were created in the knee joints of immune‐deficient rats that were treated as Group A, untreated (without transplantation); Group B, transplantation of a layered chondrocyte sheet containing 5.0 × 10(5) cells (layered chondrocyte sheet transplantation); Group C, transplantation of a synoviocyte sheet containing 5.0 × 10(5) cells (synoviocyte sheet transplantation); or Group D, transplantation of both a synoviocyte sheet plus a layered chondrocyte sheet, each containing 5.0 × 10(5) cells (synoviocyte sheet plus layered chondrocyte sheet transplantation). Histological evaluation demonstrated that Group B showed cartilage regeneration with hyaline cartilage and fibrocartilage. In Groups C and D, the defect was filled with fibrous tissue but no hyaline cartilage. Transplanted cells were detected at 4 and 12 weeks after transplantation, but the number of cells had decreased at 12 weeks. Our results indicate that layered chondrocyte sheet transplantation contributes to articular cartilage regeneration; this model proved useful for evaluating these regenerative effects.
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spelling pubmed-75406692020-10-15 Regenerative effects of human chondrocyte sheets in a xenogeneic transplantation model using immune‐deficient rats Takizawa, Daichi Sato, Masato Okada, Eri Takahashi, Takumi Maehara, Miki Tominaga, Ayako Sogo, Yasuyuki Toyoda, Eriko Watanabe, Masahiko J Tissue Eng Regen Med Research Articles Although cell transplantation has attracted much attention in regenerative medicine, animal models continue to be used in translational research to evaluate safety and efficacy because cell sources and transplantation modalities are so diverse. In the present study, we investigated the regenerative effects of human chondrocyte sheets on articular cartilage in a xenogeneic transplantation model using immune‐deficient rats. Osteochondral defects were created in the knee joints of immune‐deficient rats that were treated as Group A, untreated (without transplantation); Group B, transplantation of a layered chondrocyte sheet containing 5.0 × 10(5) cells (layered chondrocyte sheet transplantation); Group C, transplantation of a synoviocyte sheet containing 5.0 × 10(5) cells (synoviocyte sheet transplantation); or Group D, transplantation of both a synoviocyte sheet plus a layered chondrocyte sheet, each containing 5.0 × 10(5) cells (synoviocyte sheet plus layered chondrocyte sheet transplantation). Histological evaluation demonstrated that Group B showed cartilage regeneration with hyaline cartilage and fibrocartilage. In Groups C and D, the defect was filled with fibrous tissue but no hyaline cartilage. Transplanted cells were detected at 4 and 12 weeks after transplantation, but the number of cells had decreased at 12 weeks. Our results indicate that layered chondrocyte sheet transplantation contributes to articular cartilage regeneration; this model proved useful for evaluating these regenerative effects. John Wiley and Sons Inc. 2020-07-22 2020-09 /pmc/articles/PMC7540669/ /pubmed/32652894 http://dx.doi.org/10.1002/term.3101 Text en © 2020 The Authors. Journal of Tissue Engineering and Regenerative Medicine published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Takizawa, Daichi
Sato, Masato
Okada, Eri
Takahashi, Takumi
Maehara, Miki
Tominaga, Ayako
Sogo, Yasuyuki
Toyoda, Eriko
Watanabe, Masahiko
Regenerative effects of human chondrocyte sheets in a xenogeneic transplantation model using immune‐deficient rats
title Regenerative effects of human chondrocyte sheets in a xenogeneic transplantation model using immune‐deficient rats
title_full Regenerative effects of human chondrocyte sheets in a xenogeneic transplantation model using immune‐deficient rats
title_fullStr Regenerative effects of human chondrocyte sheets in a xenogeneic transplantation model using immune‐deficient rats
title_full_unstemmed Regenerative effects of human chondrocyte sheets in a xenogeneic transplantation model using immune‐deficient rats
title_short Regenerative effects of human chondrocyte sheets in a xenogeneic transplantation model using immune‐deficient rats
title_sort regenerative effects of human chondrocyte sheets in a xenogeneic transplantation model using immune‐deficient rats
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7540669/
https://www.ncbi.nlm.nih.gov/pubmed/32652894
http://dx.doi.org/10.1002/term.3101
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