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Engineered combinatorial cell device for wound healing and bone regeneration

Growth factors are the key regulators that promote tissue regeneration and healing processes. While the effects of individual growth factors are well documented, a combination of multiple secreted growth factors underlies stem cell–mediated regeneration. To avoid the potential dangers and labor-inte...

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Autores principales: Kadunc Polajnar, Lucija, Lainšček, Duško, Gašperšič, Rok, Sušjan-Leite, Petra, Kovačič, Uroš, Butinar, Miha, Turk, Boris, Jerala, Roman, Hafner-Bratkovič, Iva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10206319/
https://www.ncbi.nlm.nih.gov/pubmed/37234478
http://dx.doi.org/10.3389/fbioe.2023.1168330
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author Kadunc Polajnar, Lucija
Lainšček, Duško
Gašperšič, Rok
Sušjan-Leite, Petra
Kovačič, Uroš
Butinar, Miha
Turk, Boris
Jerala, Roman
Hafner-Bratkovič, Iva
author_facet Kadunc Polajnar, Lucija
Lainšček, Duško
Gašperšič, Rok
Sušjan-Leite, Petra
Kovačič, Uroš
Butinar, Miha
Turk, Boris
Jerala, Roman
Hafner-Bratkovič, Iva
author_sort Kadunc Polajnar, Lucija
collection PubMed
description Growth factors are the key regulators that promote tissue regeneration and healing processes. While the effects of individual growth factors are well documented, a combination of multiple secreted growth factors underlies stem cell–mediated regeneration. To avoid the potential dangers and labor-intensive individual approach of stem cell therapy while maintaining their regeneration-promoting effects based on multiple secreted growth factors, we engineered a “mix-and-match” combinatorial platform based on a library of cell lines producing growth factors. Treatment with a combination of growth factors secreted by engineered mammalian cells was more efficient than with individual growth factors or even stem cell–conditioned medium in a gap closure assay. Furthermore, we implemented in a mouse model a device for allogenic cell therapy for an in situ production of growth factors, where it improved cutaneous wound healing. Augmented bone regeneration was achieved on calvarial bone defects in rats treated with a cell device secreting IGF, FGF, PDGF, TGF-β, and VEGF. In both in vivo models, the systemic concentration of secreted factors was negligible, demonstrating the local effect of the regeneration device. Finally, we introduced a genetic switch that enables temporal control over combinations of trophic factors released at different stages of regeneration mimicking the maturation of natural wound healing to improve therapy and prevent scar formation.
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spelling pubmed-102063192023-05-25 Engineered combinatorial cell device for wound healing and bone regeneration Kadunc Polajnar, Lucija Lainšček, Duško Gašperšič, Rok Sušjan-Leite, Petra Kovačič, Uroš Butinar, Miha Turk, Boris Jerala, Roman Hafner-Bratkovič, Iva Front Bioeng Biotechnol Bioengineering and Biotechnology Growth factors are the key regulators that promote tissue regeneration and healing processes. While the effects of individual growth factors are well documented, a combination of multiple secreted growth factors underlies stem cell–mediated regeneration. To avoid the potential dangers and labor-intensive individual approach of stem cell therapy while maintaining their regeneration-promoting effects based on multiple secreted growth factors, we engineered a “mix-and-match” combinatorial platform based on a library of cell lines producing growth factors. Treatment with a combination of growth factors secreted by engineered mammalian cells was more efficient than with individual growth factors or even stem cell–conditioned medium in a gap closure assay. Furthermore, we implemented in a mouse model a device for allogenic cell therapy for an in situ production of growth factors, where it improved cutaneous wound healing. Augmented bone regeneration was achieved on calvarial bone defects in rats treated with a cell device secreting IGF, FGF, PDGF, TGF-β, and VEGF. In both in vivo models, the systemic concentration of secreted factors was negligible, demonstrating the local effect of the regeneration device. Finally, we introduced a genetic switch that enables temporal control over combinations of trophic factors released at different stages of regeneration mimicking the maturation of natural wound healing to improve therapy and prevent scar formation. Frontiers Media S.A. 2023-05-10 /pmc/articles/PMC10206319/ /pubmed/37234478 http://dx.doi.org/10.3389/fbioe.2023.1168330 Text en Copyright © 2023 Kadunc Polajnar, Lainšček, Gašperšič, Sušjan-Leite, Kovačič, Butinar, Turk, Jerala and Hafner-Bratkovič. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Kadunc Polajnar, Lucija
Lainšček, Duško
Gašperšič, Rok
Sušjan-Leite, Petra
Kovačič, Uroš
Butinar, Miha
Turk, Boris
Jerala, Roman
Hafner-Bratkovič, Iva
Engineered combinatorial cell device for wound healing and bone regeneration
title Engineered combinatorial cell device for wound healing and bone regeneration
title_full Engineered combinatorial cell device for wound healing and bone regeneration
title_fullStr Engineered combinatorial cell device for wound healing and bone regeneration
title_full_unstemmed Engineered combinatorial cell device for wound healing and bone regeneration
title_short Engineered combinatorial cell device for wound healing and bone regeneration
title_sort engineered combinatorial cell device for wound healing and bone regeneration
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10206319/
https://www.ncbi.nlm.nih.gov/pubmed/37234478
http://dx.doi.org/10.3389/fbioe.2023.1168330
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