Cargando…

Comparative study of the osteogenic potential of mesenchymal stem cells derived from different sources

BACKGROUND: Mesenchymal stem cells (MSCs) can regenerate missing tissues and treat diseases. Hence, the current work aimed to compare the proliferation rate and the osteogenic differentiation potential of bone marrow MSCs (BMSCs), gingival MSCs (GMSCs) and submandibular MSCs (SMSCs). MATERIAL AND ME...

Descripción completa

Detalles Bibliográficos
Autores principales: Aboushady, Iman M., Salem, Zeinab A., Sabry, Dina, Mohamed, Abbas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medicina Oral S.L. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5899816/
https://www.ncbi.nlm.nih.gov/pubmed/29670709
http://dx.doi.org/10.4317/jced.53957
_version_ 1783314315125719040
author Aboushady, Iman M.
Salem, Zeinab A.
Sabry, Dina
Mohamed, Abbas
author_facet Aboushady, Iman M.
Salem, Zeinab A.
Sabry, Dina
Mohamed, Abbas
author_sort Aboushady, Iman M.
collection PubMed
description BACKGROUND: Mesenchymal stem cells (MSCs) can regenerate missing tissues and treat diseases. Hence, the current work aimed to compare the proliferation rate and the osteogenic differentiation potential of bone marrow MSCs (BMSCs), gingival MSCs (GMSCs) and submandibular MSCs (SMSCs). MATERIAL AND METHODS: MSCs derived from bone marrow, gingiva and submandibular salivary gland were isolated and cultured from rats. The proliferation capacity was judged by MTT proliferation Assay. Osteogenic differentiation was assessed by Alzarin red stain and quantitative RT-PCR was performed for Runx-2 and MMP-13. RESULTS: The highest significant proliferation was estimated in the BMSCs compared to GMSCs and SMSCs (p-value was < 0.01). All studied cell types formed mineralized nodules as stained with Alizarin Red stain at the 3rd passage of differentiation. However, BMSCs seemed to generate the highest level of mineralization compared to GMSCs and SMSCs. RT-PCR revealed that the expression of Runx-2 and MMP-13 mRNAs was significantly increased in the BMSCs compared to GMSCs and SMSCs (p-value was < 0.01). CONCLUSIONS: BMSCs displayed maximum osteogenesis results followed by the GMSCs and lastly by the SGSCs. Thus, it could be recommended that GMSCs can be used as a second choice after BMSCs when bone tissue reconstruction is needed. Key words:Mesenchymal stem cells, osteogenic differentiation, Runx-2, MMP-13.
format Online
Article
Text
id pubmed-5899816
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Medicina Oral S.L.
record_format MEDLINE/PubMed
spelling pubmed-58998162018-04-18 Comparative study of the osteogenic potential of mesenchymal stem cells derived from different sources Aboushady, Iman M. Salem, Zeinab A. Sabry, Dina Mohamed, Abbas J Clin Exp Dent Research BACKGROUND: Mesenchymal stem cells (MSCs) can regenerate missing tissues and treat diseases. Hence, the current work aimed to compare the proliferation rate and the osteogenic differentiation potential of bone marrow MSCs (BMSCs), gingival MSCs (GMSCs) and submandibular MSCs (SMSCs). MATERIAL AND METHODS: MSCs derived from bone marrow, gingiva and submandibular salivary gland were isolated and cultured from rats. The proliferation capacity was judged by MTT proliferation Assay. Osteogenic differentiation was assessed by Alzarin red stain and quantitative RT-PCR was performed for Runx-2 and MMP-13. RESULTS: The highest significant proliferation was estimated in the BMSCs compared to GMSCs and SMSCs (p-value was < 0.01). All studied cell types formed mineralized nodules as stained with Alizarin Red stain at the 3rd passage of differentiation. However, BMSCs seemed to generate the highest level of mineralization compared to GMSCs and SMSCs. RT-PCR revealed that the expression of Runx-2 and MMP-13 mRNAs was significantly increased in the BMSCs compared to GMSCs and SMSCs (p-value was < 0.01). CONCLUSIONS: BMSCs displayed maximum osteogenesis results followed by the GMSCs and lastly by the SGSCs. Thus, it could be recommended that GMSCs can be used as a second choice after BMSCs when bone tissue reconstruction is needed. Key words:Mesenchymal stem cells, osteogenic differentiation, Runx-2, MMP-13. Medicina Oral S.L. 2018-01-01 /pmc/articles/PMC5899816/ /pubmed/29670709 http://dx.doi.org/10.4317/jced.53957 Text en Copyright: © 2018 Medicina Oral S.L. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Aboushady, Iman M.
Salem, Zeinab A.
Sabry, Dina
Mohamed, Abbas
Comparative study of the osteogenic potential of mesenchymal stem cells derived from different sources
title Comparative study of the osteogenic potential of mesenchymal stem cells derived from different sources
title_full Comparative study of the osteogenic potential of mesenchymal stem cells derived from different sources
title_fullStr Comparative study of the osteogenic potential of mesenchymal stem cells derived from different sources
title_full_unstemmed Comparative study of the osteogenic potential of mesenchymal stem cells derived from different sources
title_short Comparative study of the osteogenic potential of mesenchymal stem cells derived from different sources
title_sort comparative study of the osteogenic potential of mesenchymal stem cells derived from different sources
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5899816/
https://www.ncbi.nlm.nih.gov/pubmed/29670709
http://dx.doi.org/10.4317/jced.53957
work_keys_str_mv AT aboushadyimanm comparativestudyoftheosteogenicpotentialofmesenchymalstemcellsderivedfromdifferentsources
AT salemzeinaba comparativestudyoftheosteogenicpotentialofmesenchymalstemcellsderivedfromdifferentsources
AT sabrydina comparativestudyoftheosteogenicpotentialofmesenchymalstemcellsderivedfromdifferentsources
AT mohamedabbas comparativestudyoftheosteogenicpotentialofmesenchymalstemcellsderivedfromdifferentsources