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Role of chemical crosslinking in material-driven assembly of fibronectin (nano)networks: 2D surfaces and 3D scaffolds

Poly(ethyl acrylate) (PEA) induces the formation of biomimetic fibronectin (FN) (nano)networks upon simple adsorption from solutions, a process referred to as material-driven FN fibrillogenesis. The ability of PEA to organize FN has been demonstrated in 2D and 2.5D environments, but not as yet in 3D...

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Autores principales: Sabater i Serra, Roser, León-Boigues, Laia, Sánchez-Laosa, Antonio, Gómez-Estrada, Luis, Gómez Ribelles, José Luis, Salmeron-Sanchez, Manuel, Gallego Ferrer, Gloria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5109969/
https://www.ncbi.nlm.nih.gov/pubmed/27619185
http://dx.doi.org/10.1016/j.colsurfb.2016.08.044
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author Sabater i Serra, Roser
León-Boigues, Laia
Sánchez-Laosa, Antonio
Gómez-Estrada, Luis
Gómez Ribelles, José Luis
Salmeron-Sanchez, Manuel
Gallego Ferrer, Gloria
author_facet Sabater i Serra, Roser
León-Boigues, Laia
Sánchez-Laosa, Antonio
Gómez-Estrada, Luis
Gómez Ribelles, José Luis
Salmeron-Sanchez, Manuel
Gallego Ferrer, Gloria
author_sort Sabater i Serra, Roser
collection PubMed
description Poly(ethyl acrylate) (PEA) induces the formation of biomimetic fibronectin (FN) (nano)networks upon simple adsorption from solutions, a process referred to as material-driven FN fibrillogenesis. The ability of PEA to organize FN has been demonstrated in 2D and 2.5D environments, but not as yet in 3D scaffolds, which incorporate three-dimensionality and chemical crosslinkers that may influence its fibrillogenic potential. In this paper we show for the first time that while three-dimensionality does not interfere with PEA-induced FN fibrillogenesis, crosslinking does, and we determined the maximum amount of crosslinker that can be added to PEA to maintain FN fibrillogenesis. For this, we synthesised 2D substrates with different amounts of crosslinker (1–10% of ethylene glycol dimethacrylate) and studied the role of crosslinking in FN organization using AFM. The glass transition temperature was seen to increase with crosslinking density and, accordingly, polymer segmental mobility was reduced. The organization of FN after adsorption (formation of FN fibrils) and the availability of the FN cell-binding domain were found to be dependent on crosslinking density. Surface mobility was identified as a key parameter for FN supramolecular organization. PEA networks with up to 2% crosslinker organize the FN in a similar way to non-crosslinked PEA. Scaffolds prepared with 2% crosslinker also had FN (nano)networks assembled on their walls, showing PEA’s ability to induce FN fibrillogenesis in 3D environments as long as the amounts of crosslinker is low enough.
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spelling pubmed-51099692016-12-01 Role of chemical crosslinking in material-driven assembly of fibronectin (nano)networks: 2D surfaces and 3D scaffolds Sabater i Serra, Roser León-Boigues, Laia Sánchez-Laosa, Antonio Gómez-Estrada, Luis Gómez Ribelles, José Luis Salmeron-Sanchez, Manuel Gallego Ferrer, Gloria Colloids Surf B Biointerfaces Article Poly(ethyl acrylate) (PEA) induces the formation of biomimetic fibronectin (FN) (nano)networks upon simple adsorption from solutions, a process referred to as material-driven FN fibrillogenesis. The ability of PEA to organize FN has been demonstrated in 2D and 2.5D environments, but not as yet in 3D scaffolds, which incorporate three-dimensionality and chemical crosslinkers that may influence its fibrillogenic potential. In this paper we show for the first time that while three-dimensionality does not interfere with PEA-induced FN fibrillogenesis, crosslinking does, and we determined the maximum amount of crosslinker that can be added to PEA to maintain FN fibrillogenesis. For this, we synthesised 2D substrates with different amounts of crosslinker (1–10% of ethylene glycol dimethacrylate) and studied the role of crosslinking in FN organization using AFM. The glass transition temperature was seen to increase with crosslinking density and, accordingly, polymer segmental mobility was reduced. The organization of FN after adsorption (formation of FN fibrils) and the availability of the FN cell-binding domain were found to be dependent on crosslinking density. Surface mobility was identified as a key parameter for FN supramolecular organization. PEA networks with up to 2% crosslinker organize the FN in a similar way to non-crosslinked PEA. Scaffolds prepared with 2% crosslinker also had FN (nano)networks assembled on their walls, showing PEA’s ability to induce FN fibrillogenesis in 3D environments as long as the amounts of crosslinker is low enough. Elsevier 2016-12-01 /pmc/articles/PMC5109969/ /pubmed/27619185 http://dx.doi.org/10.1016/j.colsurfb.2016.08.044 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sabater i Serra, Roser
León-Boigues, Laia
Sánchez-Laosa, Antonio
Gómez-Estrada, Luis
Gómez Ribelles, José Luis
Salmeron-Sanchez, Manuel
Gallego Ferrer, Gloria
Role of chemical crosslinking in material-driven assembly of fibronectin (nano)networks: 2D surfaces and 3D scaffolds
title Role of chemical crosslinking in material-driven assembly of fibronectin (nano)networks: 2D surfaces and 3D scaffolds
title_full Role of chemical crosslinking in material-driven assembly of fibronectin (nano)networks: 2D surfaces and 3D scaffolds
title_fullStr Role of chemical crosslinking in material-driven assembly of fibronectin (nano)networks: 2D surfaces and 3D scaffolds
title_full_unstemmed Role of chemical crosslinking in material-driven assembly of fibronectin (nano)networks: 2D surfaces and 3D scaffolds
title_short Role of chemical crosslinking in material-driven assembly of fibronectin (nano)networks: 2D surfaces and 3D scaffolds
title_sort role of chemical crosslinking in material-driven assembly of fibronectin (nano)networks: 2d surfaces and 3d scaffolds
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5109969/
https://www.ncbi.nlm.nih.gov/pubmed/27619185
http://dx.doi.org/10.1016/j.colsurfb.2016.08.044
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