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Proliferation and differentiation of stem cells in contact with eluate from fibrin-rich plasma membrane

OBJECTIVE: To evaluate the ability of the eluate from fibrin-rich plasma (FRP) membrane to induce proliferation and differentiation of isolated human adipose-derived stem cells (ASCs) into chondrocytes. METHOD: FRP membranes were obtained by centrifugation of peripheral blood from two healthy donors...

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Autores principales: Souza, Fernanda Gimenez de, Fernandes, Beatriz Luci, Rebelatto, Carmen Lucia Kuniyoshi, Aguiar, Alessandra Melo de, Fracaro, Letícia, Brofman, Paulo Roberto Slud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5771793/
https://www.ncbi.nlm.nih.gov/pubmed/29367906
http://dx.doi.org/10.1016/j.rboe.2017.12.004
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author Souza, Fernanda Gimenez de
Fernandes, Beatriz Luci
Rebelatto, Carmen Lucia Kuniyoshi
Aguiar, Alessandra Melo de
Fracaro, Letícia
Brofman, Paulo Roberto Slud
author_facet Souza, Fernanda Gimenez de
Fernandes, Beatriz Luci
Rebelatto, Carmen Lucia Kuniyoshi
Aguiar, Alessandra Melo de
Fracaro, Letícia
Brofman, Paulo Roberto Slud
author_sort Souza, Fernanda Gimenez de
collection PubMed
description OBJECTIVE: To evaluate the ability of the eluate from fibrin-rich plasma (FRP) membrane to induce proliferation and differentiation of isolated human adipose-derived stem cells (ASCs) into chondrocytes. METHOD: FRP membranes were obtained by centrifugation of peripheral blood from two healthy donors, cut, and maintained in culture plate wells for 48 h to prepare the fibrin eluate. The SCATh were isolated from adipose tissue by collagenase digestion solution, and expanded in vitro. Cells were expanded and treated with DMEM-F12 culture, a commercial media for chondrogenic differentiation, and eluate from FRP membrane for three days, and labeled with BrdU for quantitative assessment of cell proliferation using the High-Content Operetta(®) imaging system. For the chondrogenic differentiation assay, the SCATh were grown in micromass for 21 days and stained with toluidine blue and aggrecan for qualitative evaluation by light microscopy. The statistical analysis was performed using ANOVA and Tukey's test. RESULTS: There was a greater proliferation of cells treated with the eluate from FRP membrane compared to the other two treatments, where the ANOVA test showed significance (p < 0.001). The differentiation into chondrocytes was visualized by the presence of mucopolysaccharide in the matrix of the cells marked in blue toluidine and aggrecan. CONCLUSIONS: Treatment with eluate from FRP membrane stimulated cell proliferation and induced differentiation of the stem cells into chondrocytes, suggesting a potential application of FRP membranes in hyaline cartilage regeneration therapies.
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spelling pubmed-57717932018-01-24 Proliferation and differentiation of stem cells in contact with eluate from fibrin-rich plasma membrane Souza, Fernanda Gimenez de Fernandes, Beatriz Luci Rebelatto, Carmen Lucia Kuniyoshi Aguiar, Alessandra Melo de Fracaro, Letícia Brofman, Paulo Roberto Slud Rev Bras Ortop Original Article OBJECTIVE: To evaluate the ability of the eluate from fibrin-rich plasma (FRP) membrane to induce proliferation and differentiation of isolated human adipose-derived stem cells (ASCs) into chondrocytes. METHOD: FRP membranes were obtained by centrifugation of peripheral blood from two healthy donors, cut, and maintained in culture plate wells for 48 h to prepare the fibrin eluate. The SCATh were isolated from adipose tissue by collagenase digestion solution, and expanded in vitro. Cells were expanded and treated with DMEM-F12 culture, a commercial media for chondrogenic differentiation, and eluate from FRP membrane for three days, and labeled with BrdU for quantitative assessment of cell proliferation using the High-Content Operetta(®) imaging system. For the chondrogenic differentiation assay, the SCATh were grown in micromass for 21 days and stained with toluidine blue and aggrecan for qualitative evaluation by light microscopy. The statistical analysis was performed using ANOVA and Tukey's test. RESULTS: There was a greater proliferation of cells treated with the eluate from FRP membrane compared to the other two treatments, where the ANOVA test showed significance (p < 0.001). The differentiation into chondrocytes was visualized by the presence of mucopolysaccharide in the matrix of the cells marked in blue toluidine and aggrecan. CONCLUSIONS: Treatment with eluate from FRP membrane stimulated cell proliferation and induced differentiation of the stem cells into chondrocytes, suggesting a potential application of FRP membranes in hyaline cartilage regeneration therapies. Elsevier 2017-12-12 /pmc/articles/PMC5771793/ /pubmed/29367906 http://dx.doi.org/10.1016/j.rboe.2017.12.004 Text en © 2017 Sociedade Brasileira de Ortopedia e Traumatologia. Published by Elsevier Editora Ltda. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Souza, Fernanda Gimenez de
Fernandes, Beatriz Luci
Rebelatto, Carmen Lucia Kuniyoshi
Aguiar, Alessandra Melo de
Fracaro, Letícia
Brofman, Paulo Roberto Slud
Proliferation and differentiation of stem cells in contact with eluate from fibrin-rich plasma membrane
title Proliferation and differentiation of stem cells in contact with eluate from fibrin-rich plasma membrane
title_full Proliferation and differentiation of stem cells in contact with eluate from fibrin-rich plasma membrane
title_fullStr Proliferation and differentiation of stem cells in contact with eluate from fibrin-rich plasma membrane
title_full_unstemmed Proliferation and differentiation of stem cells in contact with eluate from fibrin-rich plasma membrane
title_short Proliferation and differentiation of stem cells in contact with eluate from fibrin-rich plasma membrane
title_sort proliferation and differentiation of stem cells in contact with eluate from fibrin-rich plasma membrane
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5771793/
https://www.ncbi.nlm.nih.gov/pubmed/29367906
http://dx.doi.org/10.1016/j.rboe.2017.12.004
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