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The Effect of Co(0.2)Mn(0.8)Fe(2)O(4) Ferrite Nanoparticles on the C2 Canine Mastocytoma Cell Line and Adipose-Derived Mesenchymal Stromal Stem Cells (ASCs) Cultured Under a Static Magnetic Field: Possible Implications in the Treatment of Dog Mastocytoma

Cobalt manganese ferrite nanoparticles have application potential in the biomedical field, however there is limited information concerning the biological response. The aim of this work was to investigate the cytotoxic potential of cobalt-manganese ferrite nanoparticles in canine mastocytoma tumor ce...

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Autores principales: Marycz, K., Marędziak, M., Lewandowski, D., Zachanowicz, E., Zięcina, A., Wiglusz, R. J., Pązik, R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5434168/
https://www.ncbi.nlm.nih.gov/pubmed/28580034
http://dx.doi.org/10.1007/s12195-017-0480-0
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author Marycz, K.
Marędziak, M.
Lewandowski, D.
Zachanowicz, E.
Zięcina, A.
Wiglusz, R. J.
Pązik, R.
author_facet Marycz, K.
Marędziak, M.
Lewandowski, D.
Zachanowicz, E.
Zięcina, A.
Wiglusz, R. J.
Pązik, R.
author_sort Marycz, K.
collection PubMed
description Cobalt manganese ferrite nanoparticles have application potential in the biomedical field, however there is limited information concerning the biological response. The aim of this work was to investigate the cytotoxic potential of cobalt-manganese ferrite nanoparticles in canine mastocytoma tumor cells (C2) and adipose-derived mesenchymal stromal stem cells (ASCs) cultured under a static magnetic field (MF). In this study, we investigated the viability and proliferation rate of ASC and C2 cells cultured with Co(0.2)Mn(0.8)Fe(2)O(4) nanoparticles under 0.5T MF. We observed cells morphology and measured intracellular ROS generation. Thermal observations were used to characterize the thermotrophic cell behavior in different condition and RNA level of heat shock proteins and apoptotic genes was measured. Nanoparticles reduced cell viability, caused cell damage, i.e., through the formation of reactive oxygen species (ROS) and increased transcriptional level of apoptotic genes (Bcl-2, Bax, p53, p21). In addition, we have found that C2 mastocytoma cells cultured with metal oxide nanoparticles under MF exhibited unexpected biological responses, including thermotolerance and apoptotic response induced by the expression of heat shock proteins and ROS produced under a MF. Our results suggest that stimulation using MF and Co(0.2)Mn(0.8)Fe(2)O(4) nanoparticles is involved in mechanisms associated with controlling cell proliferative potential signaling events. We can state that significant differences between normal and cancer cells in response to nanoparticles and MF are apparent. Our results show that nanoparticles and MF elevate the temperature in vitro in tumor cells, thereby increasing the expression of ROS as well as heat shock proteins. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s12195-017-0480-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-54341682017-05-31 The Effect of Co(0.2)Mn(0.8)Fe(2)O(4) Ferrite Nanoparticles on the C2 Canine Mastocytoma Cell Line and Adipose-Derived Mesenchymal Stromal Stem Cells (ASCs) Cultured Under a Static Magnetic Field: Possible Implications in the Treatment of Dog Mastocytoma Marycz, K. Marędziak, M. Lewandowski, D. Zachanowicz, E. Zięcina, A. Wiglusz, R. J. Pązik, R. Cell Mol Bioeng Article Cobalt manganese ferrite nanoparticles have application potential in the biomedical field, however there is limited information concerning the biological response. The aim of this work was to investigate the cytotoxic potential of cobalt-manganese ferrite nanoparticles in canine mastocytoma tumor cells (C2) and adipose-derived mesenchymal stromal stem cells (ASCs) cultured under a static magnetic field (MF). In this study, we investigated the viability and proliferation rate of ASC and C2 cells cultured with Co(0.2)Mn(0.8)Fe(2)O(4) nanoparticles under 0.5T MF. We observed cells morphology and measured intracellular ROS generation. Thermal observations were used to characterize the thermotrophic cell behavior in different condition and RNA level of heat shock proteins and apoptotic genes was measured. Nanoparticles reduced cell viability, caused cell damage, i.e., through the formation of reactive oxygen species (ROS) and increased transcriptional level of apoptotic genes (Bcl-2, Bax, p53, p21). In addition, we have found that C2 mastocytoma cells cultured with metal oxide nanoparticles under MF exhibited unexpected biological responses, including thermotolerance and apoptotic response induced by the expression of heat shock proteins and ROS produced under a MF. Our results suggest that stimulation using MF and Co(0.2)Mn(0.8)Fe(2)O(4) nanoparticles is involved in mechanisms associated with controlling cell proliferative potential signaling events. We can state that significant differences between normal and cancer cells in response to nanoparticles and MF are apparent. Our results show that nanoparticles and MF elevate the temperature in vitro in tumor cells, thereby increasing the expression of ROS as well as heat shock proteins. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s12195-017-0480-0) contains supplementary material, which is available to authorized users. Springer US 2017-02-21 /pmc/articles/PMC5434168/ /pubmed/28580034 http://dx.doi.org/10.1007/s12195-017-0480-0 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Article
Marycz, K.
Marędziak, M.
Lewandowski, D.
Zachanowicz, E.
Zięcina, A.
Wiglusz, R. J.
Pązik, R.
The Effect of Co(0.2)Mn(0.8)Fe(2)O(4) Ferrite Nanoparticles on the C2 Canine Mastocytoma Cell Line and Adipose-Derived Mesenchymal Stromal Stem Cells (ASCs) Cultured Under a Static Magnetic Field: Possible Implications in the Treatment of Dog Mastocytoma
title The Effect of Co(0.2)Mn(0.8)Fe(2)O(4) Ferrite Nanoparticles on the C2 Canine Mastocytoma Cell Line and Adipose-Derived Mesenchymal Stromal Stem Cells (ASCs) Cultured Under a Static Magnetic Field: Possible Implications in the Treatment of Dog Mastocytoma
title_full The Effect of Co(0.2)Mn(0.8)Fe(2)O(4) Ferrite Nanoparticles on the C2 Canine Mastocytoma Cell Line and Adipose-Derived Mesenchymal Stromal Stem Cells (ASCs) Cultured Under a Static Magnetic Field: Possible Implications in the Treatment of Dog Mastocytoma
title_fullStr The Effect of Co(0.2)Mn(0.8)Fe(2)O(4) Ferrite Nanoparticles on the C2 Canine Mastocytoma Cell Line and Adipose-Derived Mesenchymal Stromal Stem Cells (ASCs) Cultured Under a Static Magnetic Field: Possible Implications in the Treatment of Dog Mastocytoma
title_full_unstemmed The Effect of Co(0.2)Mn(0.8)Fe(2)O(4) Ferrite Nanoparticles on the C2 Canine Mastocytoma Cell Line and Adipose-Derived Mesenchymal Stromal Stem Cells (ASCs) Cultured Under a Static Magnetic Field: Possible Implications in the Treatment of Dog Mastocytoma
title_short The Effect of Co(0.2)Mn(0.8)Fe(2)O(4) Ferrite Nanoparticles on the C2 Canine Mastocytoma Cell Line and Adipose-Derived Mesenchymal Stromal Stem Cells (ASCs) Cultured Under a Static Magnetic Field: Possible Implications in the Treatment of Dog Mastocytoma
title_sort effect of co(0.2)mn(0.8)fe(2)o(4) ferrite nanoparticles on the c2 canine mastocytoma cell line and adipose-derived mesenchymal stromal stem cells (ascs) cultured under a static magnetic field: possible implications in the treatment of dog mastocytoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5434168/
https://www.ncbi.nlm.nih.gov/pubmed/28580034
http://dx.doi.org/10.1007/s12195-017-0480-0
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