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Therapeutic Potential of Multilineage-Differentiating Stress-Enduring Cells for Osteochondral Repair in a Rat Model
Multilineage-differentiating stress-enduring (Muse) cells are stage-specific embryonic antigen-3 (SSEA-3) positive cells existing in mesenchymal stem cell (MSC) populations. Muse cells have the pluripotency to differentiate into all germ layers as embryonic stem cells. In this study, we aimed to inv...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5682088/ https://www.ncbi.nlm.nih.gov/pubmed/29312455 http://dx.doi.org/10.1155/2017/8154569 |
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author | Mahmoud, Elhussein Elbadry Kamei, Naosuke Shimizu, Ryo Wakao, Shohei Dezawa, Mari Adachi, Nobuo Ochi, Mitsuo |
author_facet | Mahmoud, Elhussein Elbadry Kamei, Naosuke Shimizu, Ryo Wakao, Shohei Dezawa, Mari Adachi, Nobuo Ochi, Mitsuo |
author_sort | Mahmoud, Elhussein Elbadry |
collection | PubMed |
description | Multilineage-differentiating stress-enduring (Muse) cells are stage-specific embryonic antigen-3 (SSEA-3) positive cells existing in mesenchymal stem cell (MSC) populations. Muse cells have the pluripotency to differentiate into all germ layers as embryonic stem cells. In this study, we aimed to investigate the efficacy of Muse cell transplantation for osteochondral defect repair. Muse cells were isolated from human bone marrow MSCs. An osteochondral defect was created in the patellar groove of immunodeficient rats. After this, cell injection was performed, whereby rats were divided into 3 groups: the control group, the rats of which were given a PBS injection; the non-Muse group, which comprised 5 × 10(4) SSEA-3 negative non-Muse cells; and the Muse group, which comprised 5 × 10(4) SSEA-3 positive Muse cells. The white repaired tissue had a mostly smooth homogenous surface at 12 weeks after treatment in the Muse group, while no repair tissue was detected in the control and non-Muse groups. Histological assessments showed better repair at the cartilage defect sites in the Muse group compared to the other groups at 4 and 12 weeks after treatment. Muse cells could be a new promising cell source for the treatment of osteochondral defects. |
format | Online Article Text |
id | pubmed-5682088 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-56820882018-01-08 Therapeutic Potential of Multilineage-Differentiating Stress-Enduring Cells for Osteochondral Repair in a Rat Model Mahmoud, Elhussein Elbadry Kamei, Naosuke Shimizu, Ryo Wakao, Shohei Dezawa, Mari Adachi, Nobuo Ochi, Mitsuo Stem Cells Int Research Article Multilineage-differentiating stress-enduring (Muse) cells are stage-specific embryonic antigen-3 (SSEA-3) positive cells existing in mesenchymal stem cell (MSC) populations. Muse cells have the pluripotency to differentiate into all germ layers as embryonic stem cells. In this study, we aimed to investigate the efficacy of Muse cell transplantation for osteochondral defect repair. Muse cells were isolated from human bone marrow MSCs. An osteochondral defect was created in the patellar groove of immunodeficient rats. After this, cell injection was performed, whereby rats were divided into 3 groups: the control group, the rats of which were given a PBS injection; the non-Muse group, which comprised 5 × 10(4) SSEA-3 negative non-Muse cells; and the Muse group, which comprised 5 × 10(4) SSEA-3 positive Muse cells. The white repaired tissue had a mostly smooth homogenous surface at 12 weeks after treatment in the Muse group, while no repair tissue was detected in the control and non-Muse groups. Histological assessments showed better repair at the cartilage defect sites in the Muse group compared to the other groups at 4 and 12 weeks after treatment. Muse cells could be a new promising cell source for the treatment of osteochondral defects. Hindawi 2017 2017-10-29 /pmc/articles/PMC5682088/ /pubmed/29312455 http://dx.doi.org/10.1155/2017/8154569 Text en Copyright © 2017 Elhussein Elbadry Mahmoud et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Mahmoud, Elhussein Elbadry Kamei, Naosuke Shimizu, Ryo Wakao, Shohei Dezawa, Mari Adachi, Nobuo Ochi, Mitsuo Therapeutic Potential of Multilineage-Differentiating Stress-Enduring Cells for Osteochondral Repair in a Rat Model |
title | Therapeutic Potential of Multilineage-Differentiating Stress-Enduring Cells for Osteochondral Repair in a Rat Model |
title_full | Therapeutic Potential of Multilineage-Differentiating Stress-Enduring Cells for Osteochondral Repair in a Rat Model |
title_fullStr | Therapeutic Potential of Multilineage-Differentiating Stress-Enduring Cells for Osteochondral Repair in a Rat Model |
title_full_unstemmed | Therapeutic Potential of Multilineage-Differentiating Stress-Enduring Cells for Osteochondral Repair in a Rat Model |
title_short | Therapeutic Potential of Multilineage-Differentiating Stress-Enduring Cells for Osteochondral Repair in a Rat Model |
title_sort | therapeutic potential of multilineage-differentiating stress-enduring cells for osteochondral repair in a rat model |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5682088/ https://www.ncbi.nlm.nih.gov/pubmed/29312455 http://dx.doi.org/10.1155/2017/8154569 |
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