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Electrochemical control of bone microstructure on electroactive surfaces for modulation of stem cells and bone tissue engineering

Controlling stem cell behavior at the material interface is crucial for the development of novel technologies in stem cell biology and regenerative medicine. The composition and presentation of bio-factors on a surface strongly influence the activity of stem cells. Herein, we designed an electroacti...

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Autores principales: Cao, Danfeng, Martinez, Jose G., Anada, Risa, Hara, Emilio Satoshi, Kamioka, Hiroshi, Jager, Edwin W. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10013253/
https://www.ncbi.nlm.nih.gov/pubmed/36926200
http://dx.doi.org/10.1080/14686996.2023.2183710
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author Cao, Danfeng
Martinez, Jose G.
Anada, Risa
Hara, Emilio Satoshi
Kamioka, Hiroshi
Jager, Edwin W. H.
author_facet Cao, Danfeng
Martinez, Jose G.
Anada, Risa
Hara, Emilio Satoshi
Kamioka, Hiroshi
Jager, Edwin W. H.
author_sort Cao, Danfeng
collection PubMed
description Controlling stem cell behavior at the material interface is crucial for the development of novel technologies in stem cell biology and regenerative medicine. The composition and presentation of bio-factors on a surface strongly influence the activity of stem cells. Herein, we designed an electroactive surface that mimics the initial process of trabecular bone formation, by immobilizing chondrocyte-derived plasma membrane nanofragments (PMNFs) on its surface for rapid mineralization within 2 days. Moreover, the electroactive surface was based on the conducting polymer polypyrrole (PPy), which enabled dynamic control of the presentation of PMNFs on the surface via electrochemical redox switching, further resulting in the formation of bone minerals with different morphologies. Furthermore, bone minerals with contrasting surface morphologies had differential effects on the differentiation of human bone marrow-derived stem cells (hBMSCs) cultured on the surface. Together, this electroactive surface showed multifunctional characteristics, not only allowing dynamic control of PMNF presentation but also promoting the formation of bone minerals with different morphologies within 2 days. This electroactive substrate could be valuable for more precise control of stem cell growth and differentiation, and further development of more suitable microenvironments containing bone apatite for housing a bone marrow stem cell niche, such as biochips/bone-on-chips.
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spelling pubmed-100132532023-03-15 Electrochemical control of bone microstructure on electroactive surfaces for modulation of stem cells and bone tissue engineering Cao, Danfeng Martinez, Jose G. Anada, Risa Hara, Emilio Satoshi Kamioka, Hiroshi Jager, Edwin W. H. Sci Technol Adv Mater Bio-Inspired and Biomedical Materials Controlling stem cell behavior at the material interface is crucial for the development of novel technologies in stem cell biology and regenerative medicine. The composition and presentation of bio-factors on a surface strongly influence the activity of stem cells. Herein, we designed an electroactive surface that mimics the initial process of trabecular bone formation, by immobilizing chondrocyte-derived plasma membrane nanofragments (PMNFs) on its surface for rapid mineralization within 2 days. Moreover, the electroactive surface was based on the conducting polymer polypyrrole (PPy), which enabled dynamic control of the presentation of PMNFs on the surface via electrochemical redox switching, further resulting in the formation of bone minerals with different morphologies. Furthermore, bone minerals with contrasting surface morphologies had differential effects on the differentiation of human bone marrow-derived stem cells (hBMSCs) cultured on the surface. Together, this electroactive surface showed multifunctional characteristics, not only allowing dynamic control of PMNF presentation but also promoting the formation of bone minerals with different morphologies within 2 days. This electroactive substrate could be valuable for more precise control of stem cell growth and differentiation, and further development of more suitable microenvironments containing bone apatite for housing a bone marrow stem cell niche, such as biochips/bone-on-chips. Taylor & Francis 2023-03-10 /pmc/articles/PMC10013253/ /pubmed/36926200 http://dx.doi.org/10.1080/14686996.2023.2183710 Text en © 2023 The Author(s). Published by National Institute for Materials Science in partnership with Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Bio-Inspired and Biomedical Materials
Cao, Danfeng
Martinez, Jose G.
Anada, Risa
Hara, Emilio Satoshi
Kamioka, Hiroshi
Jager, Edwin W. H.
Electrochemical control of bone microstructure on electroactive surfaces for modulation of stem cells and bone tissue engineering
title Electrochemical control of bone microstructure on electroactive surfaces for modulation of stem cells and bone tissue engineering
title_full Electrochemical control of bone microstructure on electroactive surfaces for modulation of stem cells and bone tissue engineering
title_fullStr Electrochemical control of bone microstructure on electroactive surfaces for modulation of stem cells and bone tissue engineering
title_full_unstemmed Electrochemical control of bone microstructure on electroactive surfaces for modulation of stem cells and bone tissue engineering
title_short Electrochemical control of bone microstructure on electroactive surfaces for modulation of stem cells and bone tissue engineering
title_sort electrochemical control of bone microstructure on electroactive surfaces for modulation of stem cells and bone tissue engineering
topic Bio-Inspired and Biomedical Materials
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10013253/
https://www.ncbi.nlm.nih.gov/pubmed/36926200
http://dx.doi.org/10.1080/14686996.2023.2183710
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