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Material-driven fibronectin assembly for high-efficiency presentation of growth factors
Growth factors (GFs) are powerful signaling molecules with the potential to drive regenerative strategies, including bone repair and vascularization. However, GFs are typically delivered in soluble format at supraphysiological doses because of rapid clearance and limited therapeutic impact. These hi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5001810/ https://www.ncbi.nlm.nih.gov/pubmed/27574702 http://dx.doi.org/10.1126/sciadv.1600188 |
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author | Llopis-Hernández, Virginia Cantini, Marco González-García, Cristina Cheng, Zhe A. Yang, Jingli Tsimbouri, Penelope M García, Andrés J. Dalby, Matthew J. Salmerón-Sánchez, Manuel |
author_facet | Llopis-Hernández, Virginia Cantini, Marco González-García, Cristina Cheng, Zhe A. Yang, Jingli Tsimbouri, Penelope M García, Andrés J. Dalby, Matthew J. Salmerón-Sánchez, Manuel |
author_sort | Llopis-Hernández, Virginia |
collection | PubMed |
description | Growth factors (GFs) are powerful signaling molecules with the potential to drive regenerative strategies, including bone repair and vascularization. However, GFs are typically delivered in soluble format at supraphysiological doses because of rapid clearance and limited therapeutic impact. These high doses have serious side effects and are expensive. Although it is well established that GF interactions with extracellular matrix proteins such as fibronectin control GF presentation and activity, a translation-ready approach to unlocking GF potential has not been realized. We demonstrate a simple, robust, and controlled material-based approach to enhance the activity of GFs during tissue healing. The underlying mechanism is based on spontaneous fibrillar organization of fibronectin driven by adsorption onto the polymer poly(ethyl acrylate). Fibrillar fibronectin on this polymer, but not a globular conformation obtained on control polymers, promotes synergistic presentation of integrin-binding sites and bound bone morphogenetic protein 2 (BMP-2), which enhances mesenchymal stem cell osteogenesis in vitro and drives full regeneration of a nonhealing bone defect in vivo at low GF concentrations. This simple and translatable technology could unlock the full regenerative potential of GF therapies while improving safety and cost-effectiveness. |
format | Online Article Text |
id | pubmed-5001810 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-50018102016-08-29 Material-driven fibronectin assembly for high-efficiency presentation of growth factors Llopis-Hernández, Virginia Cantini, Marco González-García, Cristina Cheng, Zhe A. Yang, Jingli Tsimbouri, Penelope M García, Andrés J. Dalby, Matthew J. Salmerón-Sánchez, Manuel Sci Adv Research Articles Growth factors (GFs) are powerful signaling molecules with the potential to drive regenerative strategies, including bone repair and vascularization. However, GFs are typically delivered in soluble format at supraphysiological doses because of rapid clearance and limited therapeutic impact. These high doses have serious side effects and are expensive. Although it is well established that GF interactions with extracellular matrix proteins such as fibronectin control GF presentation and activity, a translation-ready approach to unlocking GF potential has not been realized. We demonstrate a simple, robust, and controlled material-based approach to enhance the activity of GFs during tissue healing. The underlying mechanism is based on spontaneous fibrillar organization of fibronectin driven by adsorption onto the polymer poly(ethyl acrylate). Fibrillar fibronectin on this polymer, but not a globular conformation obtained on control polymers, promotes synergistic presentation of integrin-binding sites and bound bone morphogenetic protein 2 (BMP-2), which enhances mesenchymal stem cell osteogenesis in vitro and drives full regeneration of a nonhealing bone defect in vivo at low GF concentrations. This simple and translatable technology could unlock the full regenerative potential of GF therapies while improving safety and cost-effectiveness. American Association for the Advancement of Science 2016-08-26 /pmc/articles/PMC5001810/ /pubmed/27574702 http://dx.doi.org/10.1126/sciadv.1600188 Text en Copyright © 2016, The Authors http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Llopis-Hernández, Virginia Cantini, Marco González-García, Cristina Cheng, Zhe A. Yang, Jingli Tsimbouri, Penelope M García, Andrés J. Dalby, Matthew J. Salmerón-Sánchez, Manuel Material-driven fibronectin assembly for high-efficiency presentation of growth factors |
title | Material-driven fibronectin assembly for high-efficiency presentation of growth factors |
title_full | Material-driven fibronectin assembly for high-efficiency presentation of growth factors |
title_fullStr | Material-driven fibronectin assembly for high-efficiency presentation of growth factors |
title_full_unstemmed | Material-driven fibronectin assembly for high-efficiency presentation of growth factors |
title_short | Material-driven fibronectin assembly for high-efficiency presentation of growth factors |
title_sort | material-driven fibronectin assembly for high-efficiency presentation of growth factors |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5001810/ https://www.ncbi.nlm.nih.gov/pubmed/27574702 http://dx.doi.org/10.1126/sciadv.1600188 |
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