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Directing Stem Cell Commitment by Amorphous Calcium Phosphate Nanoparticles Incorporated in PLGA: Relevance of the Free Calcium Ion Concentration

The microenvironment of mesenchymal stem cells (MSCs) is responsible for the modulation in MSC commitment. Nanocomposites with an inorganic and an organic component have been investigated, and osteogenesis of MSCs has been attributed to inorganic phases such as calcium phosphate under several condit...

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Autores principales: Gröninger, Olivier, Hess, Samuel, Mohn, Dirk, Schneider, Elia, Stark, Wendelin, Märsmann, Sonja, Wolint, Petra, Calcagni, Maurizio, Cinelli, Paolo, Buschmann, Johanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7177725/
https://www.ncbi.nlm.nih.gov/pubmed/32283864
http://dx.doi.org/10.3390/ijms21072627
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author Gröninger, Olivier
Hess, Samuel
Mohn, Dirk
Schneider, Elia
Stark, Wendelin
Märsmann, Sonja
Wolint, Petra
Calcagni, Maurizio
Cinelli, Paolo
Buschmann, Johanna
author_facet Gröninger, Olivier
Hess, Samuel
Mohn, Dirk
Schneider, Elia
Stark, Wendelin
Märsmann, Sonja
Wolint, Petra
Calcagni, Maurizio
Cinelli, Paolo
Buschmann, Johanna
author_sort Gröninger, Olivier
collection PubMed
description The microenvironment of mesenchymal stem cells (MSCs) is responsible for the modulation in MSC commitment. Nanocomposites with an inorganic and an organic component have been investigated, and osteogenesis of MSCs has been attributed to inorganic phases such as calcium phosphate under several conditions. Here, electrospun meshes and two-dimensional films of poly(lactic-co-glycolic acid) (PLGA) or nanocomposites of PLGA and amorphous calcium phosphate nanoparticles (PLGA/aCaP) seeded with human adipose-derived stem cells (ASCs) were analyzed for the expression of selected marker genes. In a two-week in vitro experiment, osteogenic commitment was not found to be favored on PLGA/aCaP compared to pure PLGA. Analysis of the medium revealed a significant reduction of the Ca(2+) concentration when incubated with PLGA/aCaP, caused by chemical precipitation of hydroxyapatite (HAp) on aCaP seeds of PLGA/aCaP. Upon offering a constant Ca(2+) concentration, however, the previously observed anti-osteogenic effect was reversed: alkaline phosphatase, an early osteogenic marker gene, was upregulated on PLGA/aCaP compared to pristine PLGA. Hence, in addition to the cell–material interaction, the material–medium interaction was also important for the stem cell commitment here, affecting the cell–medium interaction. Complex in vitro models should therefore consider all factors, as coupled impacts might emerge.
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spelling pubmed-71777252020-04-28 Directing Stem Cell Commitment by Amorphous Calcium Phosphate Nanoparticles Incorporated in PLGA: Relevance of the Free Calcium Ion Concentration Gröninger, Olivier Hess, Samuel Mohn, Dirk Schneider, Elia Stark, Wendelin Märsmann, Sonja Wolint, Petra Calcagni, Maurizio Cinelli, Paolo Buschmann, Johanna Int J Mol Sci Article The microenvironment of mesenchymal stem cells (MSCs) is responsible for the modulation in MSC commitment. Nanocomposites with an inorganic and an organic component have been investigated, and osteogenesis of MSCs has been attributed to inorganic phases such as calcium phosphate under several conditions. Here, electrospun meshes and two-dimensional films of poly(lactic-co-glycolic acid) (PLGA) or nanocomposites of PLGA and amorphous calcium phosphate nanoparticles (PLGA/aCaP) seeded with human adipose-derived stem cells (ASCs) were analyzed for the expression of selected marker genes. In a two-week in vitro experiment, osteogenic commitment was not found to be favored on PLGA/aCaP compared to pure PLGA. Analysis of the medium revealed a significant reduction of the Ca(2+) concentration when incubated with PLGA/aCaP, caused by chemical precipitation of hydroxyapatite (HAp) on aCaP seeds of PLGA/aCaP. Upon offering a constant Ca(2+) concentration, however, the previously observed anti-osteogenic effect was reversed: alkaline phosphatase, an early osteogenic marker gene, was upregulated on PLGA/aCaP compared to pristine PLGA. Hence, in addition to the cell–material interaction, the material–medium interaction was also important for the stem cell commitment here, affecting the cell–medium interaction. Complex in vitro models should therefore consider all factors, as coupled impacts might emerge. MDPI 2020-04-09 /pmc/articles/PMC7177725/ /pubmed/32283864 http://dx.doi.org/10.3390/ijms21072627 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Gröninger, Olivier
Hess, Samuel
Mohn, Dirk
Schneider, Elia
Stark, Wendelin
Märsmann, Sonja
Wolint, Petra
Calcagni, Maurizio
Cinelli, Paolo
Buschmann, Johanna
Directing Stem Cell Commitment by Amorphous Calcium Phosphate Nanoparticles Incorporated in PLGA: Relevance of the Free Calcium Ion Concentration
title Directing Stem Cell Commitment by Amorphous Calcium Phosphate Nanoparticles Incorporated in PLGA: Relevance of the Free Calcium Ion Concentration
title_full Directing Stem Cell Commitment by Amorphous Calcium Phosphate Nanoparticles Incorporated in PLGA: Relevance of the Free Calcium Ion Concentration
title_fullStr Directing Stem Cell Commitment by Amorphous Calcium Phosphate Nanoparticles Incorporated in PLGA: Relevance of the Free Calcium Ion Concentration
title_full_unstemmed Directing Stem Cell Commitment by Amorphous Calcium Phosphate Nanoparticles Incorporated in PLGA: Relevance of the Free Calcium Ion Concentration
title_short Directing Stem Cell Commitment by Amorphous Calcium Phosphate Nanoparticles Incorporated in PLGA: Relevance of the Free Calcium Ion Concentration
title_sort directing stem cell commitment by amorphous calcium phosphate nanoparticles incorporated in plga: relevance of the free calcium ion concentration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7177725/
https://www.ncbi.nlm.nih.gov/pubmed/32283864
http://dx.doi.org/10.3390/ijms21072627
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