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Platelet-derived extracellular vesicles promote osteoinduction of mesenchymal stromal cells

AIMS: Platelet concentrates, like platelet-rich plasma (PRP) and platelet lysate (PL), are widely used in regenerative medicine, especially in bone regeneration. However, the lack of standard procedures and controls leads to high variability in the obtained results, limiting their regular clinical u...

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Autores principales: Antich-Rosselló, Miquel, Forteza-Genestra, Maria Antònia, Calvo, Javier, Gayà, Antoni, Monjo, Marta, Ramis, Joana M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The British Editorial Society of Bone & Joint Surgery 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7563034/
https://www.ncbi.nlm.nih.gov/pubmed/33101656
http://dx.doi.org/10.1302/2046-3758.910.BJR-2020-0111.R2
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author Antich-Rosselló, Miquel
Forteza-Genestra, Maria Antònia
Calvo, Javier
Gayà, Antoni
Monjo, Marta
Ramis, Joana M.
author_facet Antich-Rosselló, Miquel
Forteza-Genestra, Maria Antònia
Calvo, Javier
Gayà, Antoni
Monjo, Marta
Ramis, Joana M.
author_sort Antich-Rosselló, Miquel
collection PubMed
description AIMS: Platelet concentrates, like platelet-rich plasma (PRP) and platelet lysate (PL), are widely used in regenerative medicine, especially in bone regeneration. However, the lack of standard procedures and controls leads to high variability in the obtained results, limiting their regular clinical use. Here, we propose the use of platelet-derived extracellular vesicles (EVs) as an off-the-shelf alternative for PRP and PL for bone regeneration. In this article, we evaluate the effect of PL-derived EVs on the biocompatibility and differentiation of mesenchymal stromal cells (MSCs). METHODS: EVs were obtained first by ultracentrifugation (UC) and then by size exclusion chromatography (SEC) from non-activated PL. EVs were characterized by transmission electron microscopy, nanoparticle tracking analysis, and the expression of CD9 and CD63 markers by western blot. The effect of the obtained EVs on osteoinduction was evaluated in vitro on human umbilical cord MSCs by messenger RNA (mRNA) expression analysis of bone markers, alkaline phosphatase activity (ALP), and calcium (Ca(2+)) content. RESULTS: Osteogenic differentiation of MSCs was confirmed when treated with UC-isolated EVs. In order to disprove that the effect was due to co-isolated proteins, EVs were isolated by SEC. Purer EVs were obtained and proved to maintain the differentiation effect on MSCs and showed a dose-dependent response. CONCLUSION: PL-derived EVs present an osteogenic capability comparable to PL treatments, emerging as an alternative able to overcome PL and PRP limitations. Cite this article: Bone Joint Res 2020;9(10):667–674.
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spelling pubmed-75630342020-10-23 Platelet-derived extracellular vesicles promote osteoinduction of mesenchymal stromal cells Antich-Rosselló, Miquel Forteza-Genestra, Maria Antònia Calvo, Javier Gayà, Antoni Monjo, Marta Ramis, Joana M. Bone Joint Res Bone Biology AIMS: Platelet concentrates, like platelet-rich plasma (PRP) and platelet lysate (PL), are widely used in regenerative medicine, especially in bone regeneration. However, the lack of standard procedures and controls leads to high variability in the obtained results, limiting their regular clinical use. Here, we propose the use of platelet-derived extracellular vesicles (EVs) as an off-the-shelf alternative for PRP and PL for bone regeneration. In this article, we evaluate the effect of PL-derived EVs on the biocompatibility and differentiation of mesenchymal stromal cells (MSCs). METHODS: EVs were obtained first by ultracentrifugation (UC) and then by size exclusion chromatography (SEC) from non-activated PL. EVs were characterized by transmission electron microscopy, nanoparticle tracking analysis, and the expression of CD9 and CD63 markers by western blot. The effect of the obtained EVs on osteoinduction was evaluated in vitro on human umbilical cord MSCs by messenger RNA (mRNA) expression analysis of bone markers, alkaline phosphatase activity (ALP), and calcium (Ca(2+)) content. RESULTS: Osteogenic differentiation of MSCs was confirmed when treated with UC-isolated EVs. In order to disprove that the effect was due to co-isolated proteins, EVs were isolated by SEC. Purer EVs were obtained and proved to maintain the differentiation effect on MSCs and showed a dose-dependent response. CONCLUSION: PL-derived EVs present an osteogenic capability comparable to PL treatments, emerging as an alternative able to overcome PL and PRP limitations. Cite this article: Bone Joint Res 2020;9(10):667–674. The British Editorial Society of Bone & Joint Surgery 2020-10-16 /pmc/articles/PMC7563034/ /pubmed/33101656 http://dx.doi.org/10.1302/2046-3758.910.BJR-2020-0111.R2 Text en © 2020 Author(s) et al. https://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (CC BY-NC-ND 4.0) licence, which permits the copying and redistribution of the work only, and provided the original author and source are credited. See https://creativecommons.org/licenses/by-nc-nd/4.0/.
spellingShingle Bone Biology
Antich-Rosselló, Miquel
Forteza-Genestra, Maria Antònia
Calvo, Javier
Gayà, Antoni
Monjo, Marta
Ramis, Joana M.
Platelet-derived extracellular vesicles promote osteoinduction of mesenchymal stromal cells
title Platelet-derived extracellular vesicles promote osteoinduction of mesenchymal stromal cells
title_full Platelet-derived extracellular vesicles promote osteoinduction of mesenchymal stromal cells
title_fullStr Platelet-derived extracellular vesicles promote osteoinduction of mesenchymal stromal cells
title_full_unstemmed Platelet-derived extracellular vesicles promote osteoinduction of mesenchymal stromal cells
title_short Platelet-derived extracellular vesicles promote osteoinduction of mesenchymal stromal cells
title_sort platelet-derived extracellular vesicles promote osteoinduction of mesenchymal stromal cells
topic Bone Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7563034/
https://www.ncbi.nlm.nih.gov/pubmed/33101656
http://dx.doi.org/10.1302/2046-3758.910.BJR-2020-0111.R2
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