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Acoustic modification of collagen hydrogels facilitates cellular remodeling
Developing tunable biomaterials that have the capacity to recreate the physical and biochemical characteristics of native extracellular matrices (ECMs) with spatial fidelity is important for a variety of biomedical, biological, and clinical applications. Several factors have made the ECM protein, co...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6853634/ https://www.ncbi.nlm.nih.gov/pubmed/31723936 http://dx.doi.org/10.1016/j.mtbio.2019.100018 |
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author | Norris, E.G. Dalecki, D. Hocking, D.C. |
author_facet | Norris, E.G. Dalecki, D. Hocking, D.C. |
author_sort | Norris, E.G. |
collection | PubMed |
description | Developing tunable biomaterials that have the capacity to recreate the physical and biochemical characteristics of native extracellular matrices (ECMs) with spatial fidelity is important for a variety of biomedical, biological, and clinical applications. Several factors have made the ECM protein, collagen I, an attractive biomaterial, including its ease of isolation, low antigenicity and toxicity, and biodegradability. However, current collagen gel formulations fail to recapitulate the range of collagen structures observed in native tissues, presenting a significant challenge in achieving the full potential of collagen-based biomaterials. Collagen fiber structure can be manipulated in vitro through mechanical forces, environmental factors, or thermal mechanisms. Here, we describe a new ultrasound-based fabrication technology that exploits the ability of ultrasound to generate localized mechanical forces to control the collagen fiber microstructure non-invasively. The results indicate that exposing soluble collagen to ultrasound (7.8 or 8.8 MHz; 3.2–10 W/cm(2)) during hydrogel formation leads to local variations in collagen fiber structure and organization that support increased levels of cell migration. Furthermore, multiphoton imaging revealed increased cell-mediated collagen remodeling of ultrasound-exposed but not sham-exposed hydrogels, including formation of multicellular aggregates, collagen fiber bundle contraction, and increased binding of collagen hybridizing peptides. Skin explant cultures obtained from diabetic mice showed similar enhancement of cell-mediated remodeling of ultrasound-exposed but not sham-exposed collagen hydrogels. Using the mechanical forces associated with ultrasound to induce local changes in collagen fibril structure and organization to functionalize native biomaterials is a promising non-invasive and non-toxic technology for tissue engineering and regenerative medicine. |
format | Online Article Text |
id | pubmed-6853634 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-68536342019-11-13 Acoustic modification of collagen hydrogels facilitates cellular remodeling Norris, E.G. Dalecki, D. Hocking, D.C. Mater Today Bio Full Length Article Developing tunable biomaterials that have the capacity to recreate the physical and biochemical characteristics of native extracellular matrices (ECMs) with spatial fidelity is important for a variety of biomedical, biological, and clinical applications. Several factors have made the ECM protein, collagen I, an attractive biomaterial, including its ease of isolation, low antigenicity and toxicity, and biodegradability. However, current collagen gel formulations fail to recapitulate the range of collagen structures observed in native tissues, presenting a significant challenge in achieving the full potential of collagen-based biomaterials. Collagen fiber structure can be manipulated in vitro through mechanical forces, environmental factors, or thermal mechanisms. Here, we describe a new ultrasound-based fabrication technology that exploits the ability of ultrasound to generate localized mechanical forces to control the collagen fiber microstructure non-invasively. The results indicate that exposing soluble collagen to ultrasound (7.8 or 8.8 MHz; 3.2–10 W/cm(2)) during hydrogel formation leads to local variations in collagen fiber structure and organization that support increased levels of cell migration. Furthermore, multiphoton imaging revealed increased cell-mediated collagen remodeling of ultrasound-exposed but not sham-exposed hydrogels, including formation of multicellular aggregates, collagen fiber bundle contraction, and increased binding of collagen hybridizing peptides. Skin explant cultures obtained from diabetic mice showed similar enhancement of cell-mediated remodeling of ultrasound-exposed but not sham-exposed collagen hydrogels. Using the mechanical forces associated with ultrasound to induce local changes in collagen fibril structure and organization to functionalize native biomaterials is a promising non-invasive and non-toxic technology for tissue engineering and regenerative medicine. Elsevier 2019-07-22 /pmc/articles/PMC6853634/ /pubmed/31723936 http://dx.doi.org/10.1016/j.mtbio.2019.100018 Text en © 2019 The Author(s) 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 | Full Length Article Norris, E.G. Dalecki, D. Hocking, D.C. Acoustic modification of collagen hydrogels facilitates cellular remodeling |
title | Acoustic modification of collagen hydrogels facilitates cellular remodeling |
title_full | Acoustic modification of collagen hydrogels facilitates cellular remodeling |
title_fullStr | Acoustic modification of collagen hydrogels facilitates cellular remodeling |
title_full_unstemmed | Acoustic modification of collagen hydrogels facilitates cellular remodeling |
title_short | Acoustic modification of collagen hydrogels facilitates cellular remodeling |
title_sort | acoustic modification of collagen hydrogels facilitates cellular remodeling |
topic | Full Length Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6853634/ https://www.ncbi.nlm.nih.gov/pubmed/31723936 http://dx.doi.org/10.1016/j.mtbio.2019.100018 |
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