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The Effect of Human Platelet-Rich Plasma on Adipose-Derived Stem Cell Proliferation and Osteogenic Differentiation

Background: The cultured mesenchymal stem cells (MSC) have been used in many clinical trials; however, there are still some concerns about the cultural conditions. One concern is related to the use of FBS as a widely used xenogeneic supplement in the culture system. Human platelet-rich plasma (hPRP)...

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Autores principales: Tavakolinejad, Sima, Khosravi, Mohsen, Mashkani, Baratali, Ebrahimzadeh Bideskan, Alireza, Sanjar Mossavi, Nasser, Parizadeh, Seyyed Mohammad Reza, Hamidi Alamdari, Daryoush
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pasteur Institute of Iran 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4048479/
https://www.ncbi.nlm.nih.gov/pubmed/24842141
http://dx.doi.org/10.6091/ibj.1301.2014
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author Tavakolinejad, Sima
Khosravi, Mohsen
Mashkani, Baratali
Ebrahimzadeh Bideskan, Alireza
Sanjar Mossavi, Nasser
Parizadeh, Seyyed Mohammad Reza
Hamidi Alamdari, Daryoush
author_facet Tavakolinejad, Sima
Khosravi, Mohsen
Mashkani, Baratali
Ebrahimzadeh Bideskan, Alireza
Sanjar Mossavi, Nasser
Parizadeh, Seyyed Mohammad Reza
Hamidi Alamdari, Daryoush
author_sort Tavakolinejad, Sima
collection PubMed
description Background: The cultured mesenchymal stem cells (MSC) have been used in many clinical trials; however, there are still some concerns about the cultural conditions. One concern is related to the use of FBS as a widely used xenogeneic supplement in the culture system. Human platelet-rich plasma (hPRP) is a candidate replacement for FBS. In this study, the effect of hPRP on MSC proliferation and osteogenic differentiation has been evaluated. Methods: Human adipose-derived stem cells (hADSC) were expanded. Cells from the third passage were characterized by flow cytometric analysis and used for in vitro experiments. Resazurin and alizarin red stains were used for cell proliferation and osteogenic differentiation assays, respectively. Results: Treatment with hPRP resulted in a statistically significant increase in cell proliferation compare to the negative control group (P<0.001). Cell proliferation in the 15% hPRP group was also significantly higher than that in the 10% hPRP group (P<0.05). Additionally, it caused less osteogenic differentiation of the hADSC compared to the FBS (P<0.001), but in comparison to negative control, it caused acceptable mineralization (P<0.001). Conclusion: These findings indicate that hPRP not only improves the proliferation but also it can be a suitable substitution in osteogenic differentiation for clinical purposes. However, the clinical application value of hPRP still needs more investigation.
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spelling pubmed-40484792014-07-01 The Effect of Human Platelet-Rich Plasma on Adipose-Derived Stem Cell Proliferation and Osteogenic Differentiation Tavakolinejad, Sima Khosravi, Mohsen Mashkani, Baratali Ebrahimzadeh Bideskan, Alireza Sanjar Mossavi, Nasser Parizadeh, Seyyed Mohammad Reza Hamidi Alamdari, Daryoush Iran Biomed J Original Article Background: The cultured mesenchymal stem cells (MSC) have been used in many clinical trials; however, there are still some concerns about the cultural conditions. One concern is related to the use of FBS as a widely used xenogeneic supplement in the culture system. Human platelet-rich plasma (hPRP) is a candidate replacement for FBS. In this study, the effect of hPRP on MSC proliferation and osteogenic differentiation has been evaluated. Methods: Human adipose-derived stem cells (hADSC) were expanded. Cells from the third passage were characterized by flow cytometric analysis and used for in vitro experiments. Resazurin and alizarin red stains were used for cell proliferation and osteogenic differentiation assays, respectively. Results: Treatment with hPRP resulted in a statistically significant increase in cell proliferation compare to the negative control group (P<0.001). Cell proliferation in the 15% hPRP group was also significantly higher than that in the 10% hPRP group (P<0.05). Additionally, it caused less osteogenic differentiation of the hADSC compared to the FBS (P<0.001), but in comparison to negative control, it caused acceptable mineralization (P<0.001). Conclusion: These findings indicate that hPRP not only improves the proliferation but also it can be a suitable substitution in osteogenic differentiation for clinical purposes. However, the clinical application value of hPRP still needs more investigation. Pasteur Institute of Iran 2014-07 /pmc/articles/PMC4048479/ /pubmed/24842141 http://dx.doi.org/10.6091/ibj.1301.2014 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Tavakolinejad, Sima
Khosravi, Mohsen
Mashkani, Baratali
Ebrahimzadeh Bideskan, Alireza
Sanjar Mossavi, Nasser
Parizadeh, Seyyed Mohammad Reza
Hamidi Alamdari, Daryoush
The Effect of Human Platelet-Rich Plasma on Adipose-Derived Stem Cell Proliferation and Osteogenic Differentiation
title The Effect of Human Platelet-Rich Plasma on Adipose-Derived Stem Cell Proliferation and Osteogenic Differentiation
title_full The Effect of Human Platelet-Rich Plasma on Adipose-Derived Stem Cell Proliferation and Osteogenic Differentiation
title_fullStr The Effect of Human Platelet-Rich Plasma on Adipose-Derived Stem Cell Proliferation and Osteogenic Differentiation
title_full_unstemmed The Effect of Human Platelet-Rich Plasma on Adipose-Derived Stem Cell Proliferation and Osteogenic Differentiation
title_short The Effect of Human Platelet-Rich Plasma on Adipose-Derived Stem Cell Proliferation and Osteogenic Differentiation
title_sort effect of human platelet-rich plasma on adipose-derived stem cell proliferation and osteogenic differentiation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4048479/
https://www.ncbi.nlm.nih.gov/pubmed/24842141
http://dx.doi.org/10.6091/ibj.1301.2014
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