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Fe-Cr-Nb-B Magnetic Particles and Adipose-Derived Mesenchymal Cells Trigger Cancer Cell Apoptosis by Magneto-Mechanical Actuation

Magnetic nanoparticles (MPs) are emerging as powerful and versatile tools for biotechnology, including cancer research and theranostic applications. Stem cell-mediated magnetic particle delivery has been previously recognized as a modality to target sites of malignancies. Here, we propose the use of...

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Autores principales: Chiriac, Horia, Minuti, Anca Emanuela, Stavila, Cristina, Herea, Dumitru-Daniel, Labusca, Luminita, Ababei, Gabriel, Stoian, George, Lupu, Nicoleta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10675303/
https://www.ncbi.nlm.nih.gov/pubmed/37999295
http://dx.doi.org/10.3390/nano13222941
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author Chiriac, Horia
Minuti, Anca Emanuela
Stavila, Cristina
Herea, Dumitru-Daniel
Labusca, Luminita
Ababei, Gabriel
Stoian, George
Lupu, Nicoleta
author_facet Chiriac, Horia
Minuti, Anca Emanuela
Stavila, Cristina
Herea, Dumitru-Daniel
Labusca, Luminita
Ababei, Gabriel
Stoian, George
Lupu, Nicoleta
author_sort Chiriac, Horia
collection PubMed
description Magnetic nanoparticles (MPs) are emerging as powerful and versatile tools for biotechnology, including cancer research and theranostic applications. Stem cell-mediated magnetic particle delivery has been previously recognized as a modality to target sites of malignancies. Here, we propose the use of adipose-derived mesenchymal cells (ADSC) for the targeted delivery of Fe-Cr-Nb-B magnetic particles to human osteosarcoma (HOS) cells and magneto-mechanical actuation (MMA) for targeting and destroying HOS cells. We show that MPs are easily incorporated by ADSCs and HOS cells, as confirmed by TEM images and a ferrozine assay. MP-loaded ADSCs display increased motility towards tumor cells compared with their unloaded counterparts. MMA of MP-loaded ADSCs induces HOS destruction, as confirmed by the MTT and live/dead assays. MMA enables the release of the MPs towards cancer cells, producing a significant decrease (about 80%) in HOS viability immediately after application. In contrast, normal human dermal fibroblasts’ (NHDFs) viability exposed to similar conditions remains high, showing a differential behavior of normal and malignant cells to MP load and MMA exposure. Taken together, the method could derive successful strategies for in vivo applications in targeting and destroying malignant cells while protecting normal cells.
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spelling pubmed-106753032023-11-14 Fe-Cr-Nb-B Magnetic Particles and Adipose-Derived Mesenchymal Cells Trigger Cancer Cell Apoptosis by Magneto-Mechanical Actuation Chiriac, Horia Minuti, Anca Emanuela Stavila, Cristina Herea, Dumitru-Daniel Labusca, Luminita Ababei, Gabriel Stoian, George Lupu, Nicoleta Nanomaterials (Basel) Article Magnetic nanoparticles (MPs) are emerging as powerful and versatile tools for biotechnology, including cancer research and theranostic applications. Stem cell-mediated magnetic particle delivery has been previously recognized as a modality to target sites of malignancies. Here, we propose the use of adipose-derived mesenchymal cells (ADSC) for the targeted delivery of Fe-Cr-Nb-B magnetic particles to human osteosarcoma (HOS) cells and magneto-mechanical actuation (MMA) for targeting and destroying HOS cells. We show that MPs are easily incorporated by ADSCs and HOS cells, as confirmed by TEM images and a ferrozine assay. MP-loaded ADSCs display increased motility towards tumor cells compared with their unloaded counterparts. MMA of MP-loaded ADSCs induces HOS destruction, as confirmed by the MTT and live/dead assays. MMA enables the release of the MPs towards cancer cells, producing a significant decrease (about 80%) in HOS viability immediately after application. In contrast, normal human dermal fibroblasts’ (NHDFs) viability exposed to similar conditions remains high, showing a differential behavior of normal and malignant cells to MP load and MMA exposure. Taken together, the method could derive successful strategies for in vivo applications in targeting and destroying malignant cells while protecting normal cells. MDPI 2023-11-14 /pmc/articles/PMC10675303/ /pubmed/37999295 http://dx.doi.org/10.3390/nano13222941 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Chiriac, Horia
Minuti, Anca Emanuela
Stavila, Cristina
Herea, Dumitru-Daniel
Labusca, Luminita
Ababei, Gabriel
Stoian, George
Lupu, Nicoleta
Fe-Cr-Nb-B Magnetic Particles and Adipose-Derived Mesenchymal Cells Trigger Cancer Cell Apoptosis by Magneto-Mechanical Actuation
title Fe-Cr-Nb-B Magnetic Particles and Adipose-Derived Mesenchymal Cells Trigger Cancer Cell Apoptosis by Magneto-Mechanical Actuation
title_full Fe-Cr-Nb-B Magnetic Particles and Adipose-Derived Mesenchymal Cells Trigger Cancer Cell Apoptosis by Magneto-Mechanical Actuation
title_fullStr Fe-Cr-Nb-B Magnetic Particles and Adipose-Derived Mesenchymal Cells Trigger Cancer Cell Apoptosis by Magneto-Mechanical Actuation
title_full_unstemmed Fe-Cr-Nb-B Magnetic Particles and Adipose-Derived Mesenchymal Cells Trigger Cancer Cell Apoptosis by Magneto-Mechanical Actuation
title_short Fe-Cr-Nb-B Magnetic Particles and Adipose-Derived Mesenchymal Cells Trigger Cancer Cell Apoptosis by Magneto-Mechanical Actuation
title_sort fe-cr-nb-b magnetic particles and adipose-derived mesenchymal cells trigger cancer cell apoptosis by magneto-mechanical actuation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10675303/
https://www.ncbi.nlm.nih.gov/pubmed/37999295
http://dx.doi.org/10.3390/nano13222941
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