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Promising Low-Toxicity of Viologen-Phosphorus Dendrimers against Embryonic Mouse Hippocampal Cells
A new class of viologen-phosphorus dendrimers (VPDs) has been recently shown to possess the ability to inhibit neurodegenerative processes in vitro. Nevertheless, in the Central Nervous Systems domain, there is little information on their impact on cell functions, especially on neuronal cells. In th...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270227/ https://www.ncbi.nlm.nih.gov/pubmed/24084024 http://dx.doi.org/10.3390/molecules181012222 |
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author | Lazniewska, Joanna Janaszewska, Anna Miłowska, Katarzyna Caminade, Anne-Marie Mignani, Serge Katir, Nadia Kadib, Abdelkrim El Bryszewska, Maria Majoral, Jean-Pierre Gabryelak, Teresa Klajnert-Maculewicz, Barbara |
author_facet | Lazniewska, Joanna Janaszewska, Anna Miłowska, Katarzyna Caminade, Anne-Marie Mignani, Serge Katir, Nadia Kadib, Abdelkrim El Bryszewska, Maria Majoral, Jean-Pierre Gabryelak, Teresa Klajnert-Maculewicz, Barbara |
author_sort | Lazniewska, Joanna |
collection | PubMed |
description | A new class of viologen-phosphorus dendrimers (VPDs) has been recently shown to possess the ability to inhibit neurodegenerative processes in vitro. Nevertheless, in the Central Nervous Systems domain, there is little information on their impact on cell functions, especially on neuronal cells. In this work, we examined the influence of two VPD (VPD1 and VPD3) of zero generation (G0) on murine hippocampal cell line (named mHippoE-18). Extended analyses of cell responses to these nanomolecules comprised cytotoxicity test, reactive oxygen species (ROS) generation studies, mitochondrial membrane potential (ΔΨm) assay, cell death detection, cell morphology assessment, cell cycle studies, as well as measurements of catalase (CAT) activity and glutathione (GSH) level. The results indicate that VPD1 is more toxic than VPD3. However, these two tested dendrimers did not cause a strong cellular response, and induced a low level of apoptosis. Interestingly, VPD1 and VPD3 treatment led to a small decline in ROS level compared to untreated cells, which correlated with slightly increased catalase activity. This result indicates that the VPDs can indirectly lower the level of ROS in cells. Summarising, low-cytotoxicity on mHippoE-18 cells together with their ability to quench ROS, make the VPDs very promising nanodevices for future applications in the biomedical field as nanocarriers and/or drugs per se. |
format | Online Article Text |
id | pubmed-6270227 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62702272018-12-18 Promising Low-Toxicity of Viologen-Phosphorus Dendrimers against Embryonic Mouse Hippocampal Cells Lazniewska, Joanna Janaszewska, Anna Miłowska, Katarzyna Caminade, Anne-Marie Mignani, Serge Katir, Nadia Kadib, Abdelkrim El Bryszewska, Maria Majoral, Jean-Pierre Gabryelak, Teresa Klajnert-Maculewicz, Barbara Molecules Article A new class of viologen-phosphorus dendrimers (VPDs) has been recently shown to possess the ability to inhibit neurodegenerative processes in vitro. Nevertheless, in the Central Nervous Systems domain, there is little information on their impact on cell functions, especially on neuronal cells. In this work, we examined the influence of two VPD (VPD1 and VPD3) of zero generation (G0) on murine hippocampal cell line (named mHippoE-18). Extended analyses of cell responses to these nanomolecules comprised cytotoxicity test, reactive oxygen species (ROS) generation studies, mitochondrial membrane potential (ΔΨm) assay, cell death detection, cell morphology assessment, cell cycle studies, as well as measurements of catalase (CAT) activity and glutathione (GSH) level. The results indicate that VPD1 is more toxic than VPD3. However, these two tested dendrimers did not cause a strong cellular response, and induced a low level of apoptosis. Interestingly, VPD1 and VPD3 treatment led to a small decline in ROS level compared to untreated cells, which correlated with slightly increased catalase activity. This result indicates that the VPDs can indirectly lower the level of ROS in cells. Summarising, low-cytotoxicity on mHippoE-18 cells together with their ability to quench ROS, make the VPDs very promising nanodevices for future applications in the biomedical field as nanocarriers and/or drugs per se. MDPI 2013-09-30 /pmc/articles/PMC6270227/ /pubmed/24084024 http://dx.doi.org/10.3390/molecules181012222 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Lazniewska, Joanna Janaszewska, Anna Miłowska, Katarzyna Caminade, Anne-Marie Mignani, Serge Katir, Nadia Kadib, Abdelkrim El Bryszewska, Maria Majoral, Jean-Pierre Gabryelak, Teresa Klajnert-Maculewicz, Barbara Promising Low-Toxicity of Viologen-Phosphorus Dendrimers against Embryonic Mouse Hippocampal Cells |
title | Promising Low-Toxicity of Viologen-Phosphorus Dendrimers against Embryonic Mouse Hippocampal Cells |
title_full | Promising Low-Toxicity of Viologen-Phosphorus Dendrimers against Embryonic Mouse Hippocampal Cells |
title_fullStr | Promising Low-Toxicity of Viologen-Phosphorus Dendrimers against Embryonic Mouse Hippocampal Cells |
title_full_unstemmed | Promising Low-Toxicity of Viologen-Phosphorus Dendrimers against Embryonic Mouse Hippocampal Cells |
title_short | Promising Low-Toxicity of Viologen-Phosphorus Dendrimers against Embryonic Mouse Hippocampal Cells |
title_sort | promising low-toxicity of viologen-phosphorus dendrimers against embryonic mouse hippocampal cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270227/ https://www.ncbi.nlm.nih.gov/pubmed/24084024 http://dx.doi.org/10.3390/molecules181012222 |
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