Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Mahmoud, Elhussein Elbadry, Kamei, Naosuke, Shimizu, Ryo, Wakao, Shohei, Dezawa, Mari, Adachi, Nobuo, Ochi, Mitsuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
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
_version_ 1783278039874928640
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
work_keys_str_mv AT mahmoudelhusseinelbadry therapeuticpotentialofmultilineagedifferentiatingstressenduringcellsforosteochondralrepairinaratmodel
AT kameinaosuke therapeuticpotentialofmultilineagedifferentiatingstressenduringcellsforosteochondralrepairinaratmodel
AT shimizuryo therapeuticpotentialofmultilineagedifferentiatingstressenduringcellsforosteochondralrepairinaratmodel
AT wakaoshohei therapeuticpotentialofmultilineagedifferentiatingstressenduringcellsforosteochondralrepairinaratmodel
AT dezawamari therapeuticpotentialofmultilineagedifferentiatingstressenduringcellsforosteochondralrepairinaratmodel
AT adachinobuo therapeuticpotentialofmultilineagedifferentiatingstressenduringcellsforosteochondralrepairinaratmodel
AT ochimitsuo therapeuticpotentialofmultilineagedifferentiatingstressenduringcellsforosteochondralrepairinaratmodel