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In vitro effects of nanoparticles on renal cells
BACKGROUND: The ability of nanoparticles to cross the lung-blood barrier suggests that they may translocate to blood and to targets distant from their portal of entry. Nevertheless, nanotoxicity in organs has received little attention. The purpose of this study was to evaluate nanotoxicity in renal...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2621238/ https://www.ncbi.nlm.nih.gov/pubmed/19099552 http://dx.doi.org/10.1186/1743-8977-5-22 |
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author | L'Azou, Béatrice Jorly, Joana On, Dinhill Sellier, Elisabeth Moisan, Frédéric Fleury-Feith, Jocelyne Cambar, Jean Brochard, Patrick Ohayon-Courtès, Céline |
author_facet | L'Azou, Béatrice Jorly, Joana On, Dinhill Sellier, Elisabeth Moisan, Frédéric Fleury-Feith, Jocelyne Cambar, Jean Brochard, Patrick Ohayon-Courtès, Céline |
author_sort | L'Azou, Béatrice |
collection | PubMed |
description | BACKGROUND: The ability of nanoparticles to cross the lung-blood barrier suggests that they may translocate to blood and to targets distant from their portal of entry. Nevertheless, nanotoxicity in organs has received little attention. The purpose of this study was to evaluate nanotoxicity in renal cells using in vitro models. Various carbon black (CB) (FW2–13 nm, Printex60-21 nm and LB101-95 nm) and titanium dioxide (TiO(2)-15 and TiO(2)-50 nm) nanoparticles were characterized on size by electron microscopy. We evaluated theirs effects on glomerular mesangial (IP15) and epithelial proximal tubular (LLC-PK(1)) renal cells, using light microscopy, WST-1 assay, immunofluorescence labeling and DCFH-DA for reactive oxygen species (ROS) assay. RESULTS: Nanoparticles induced a variety of cell responses. On both IP15 and LLC-PK(1 )cells, the smallest FW2 NP was found to be the most cytotoxic with classic dose-behavior. For the other NPs tested, different cytotoxic profiles were found, with LLC-PK(1 )cells being more sensitive than IP15 cells. Exposure to FW2 NPs, evidenced in our experiments as the most cytotoxic particle type, significantly enhanced production of ROS in both IP15 and LLC-PK(1 )cells. Immunofluorescence microscopy using latex beads indicated that depending on their size, the cells internalized particles, which accumulated in the cell cytoplasm. Additionally using transmission electronic microscope micrographs show nanoparticles inside the cells and trapped in vesicles. CONCLUSION: The present data constitute the first step towards determining in vitro dose effect of manufactured CB and TiO(2 )NPs in renal cells. Cytotoxicological assays using epithelial tubular and glomerular mesangial cell lines rapidly provide information and demonstrated that NP materials exhibit varying degrees of cytotoxicity. It seems clear that in vitro cellular systems will need to be further developed, standardized and validated (relative to in vivo effects) in order to provide useful screening data about the relative toxicity of nanoparticles. |
format | Text |
id | pubmed-2621238 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26212382009-01-13 In vitro effects of nanoparticles on renal cells L'Azou, Béatrice Jorly, Joana On, Dinhill Sellier, Elisabeth Moisan, Frédéric Fleury-Feith, Jocelyne Cambar, Jean Brochard, Patrick Ohayon-Courtès, Céline Part Fibre Toxicol Research BACKGROUND: The ability of nanoparticles to cross the lung-blood barrier suggests that they may translocate to blood and to targets distant from their portal of entry. Nevertheless, nanotoxicity in organs has received little attention. The purpose of this study was to evaluate nanotoxicity in renal cells using in vitro models. Various carbon black (CB) (FW2–13 nm, Printex60-21 nm and LB101-95 nm) and titanium dioxide (TiO(2)-15 and TiO(2)-50 nm) nanoparticles were characterized on size by electron microscopy. We evaluated theirs effects on glomerular mesangial (IP15) and epithelial proximal tubular (LLC-PK(1)) renal cells, using light microscopy, WST-1 assay, immunofluorescence labeling and DCFH-DA for reactive oxygen species (ROS) assay. RESULTS: Nanoparticles induced a variety of cell responses. On both IP15 and LLC-PK(1 )cells, the smallest FW2 NP was found to be the most cytotoxic with classic dose-behavior. For the other NPs tested, different cytotoxic profiles were found, with LLC-PK(1 )cells being more sensitive than IP15 cells. Exposure to FW2 NPs, evidenced in our experiments as the most cytotoxic particle type, significantly enhanced production of ROS in both IP15 and LLC-PK(1 )cells. Immunofluorescence microscopy using latex beads indicated that depending on their size, the cells internalized particles, which accumulated in the cell cytoplasm. Additionally using transmission electronic microscope micrographs show nanoparticles inside the cells and trapped in vesicles. CONCLUSION: The present data constitute the first step towards determining in vitro dose effect of manufactured CB and TiO(2 )NPs in renal cells. Cytotoxicological assays using epithelial tubular and glomerular mesangial cell lines rapidly provide information and demonstrated that NP materials exhibit varying degrees of cytotoxicity. It seems clear that in vitro cellular systems will need to be further developed, standardized and validated (relative to in vivo effects) in order to provide useful screening data about the relative toxicity of nanoparticles. BioMed Central 2008-12-19 /pmc/articles/PMC2621238/ /pubmed/19099552 http://dx.doi.org/10.1186/1743-8977-5-22 Text en Copyright © 2008 L'Azou et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research L'Azou, Béatrice Jorly, Joana On, Dinhill Sellier, Elisabeth Moisan, Frédéric Fleury-Feith, Jocelyne Cambar, Jean Brochard, Patrick Ohayon-Courtès, Céline In vitro effects of nanoparticles on renal cells |
title | In vitro effects of nanoparticles on renal cells |
title_full | In vitro effects of nanoparticles on renal cells |
title_fullStr | In vitro effects of nanoparticles on renal cells |
title_full_unstemmed | In vitro effects of nanoparticles on renal cells |
title_short | In vitro effects of nanoparticles on renal cells |
title_sort | in vitro effects of nanoparticles on renal cells |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2621238/ https://www.ncbi.nlm.nih.gov/pubmed/19099552 http://dx.doi.org/10.1186/1743-8977-5-22 |
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