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Endocytosed nanoparticles hold endosomes and stimulate binucleated cells formation

BACKGROUND: Nanotechnology developed rapidly in cellular diagnosis and treatment, the endocytic system was an important pathway for targeting cell. In the research of developing macrophages as drug carriers or important therapeutic targets, an interesting phenomenon, internalized nanoparticles induc...

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Autores principales: Xia, Lin, Gu, Weihong, Zhang, Mingyi, Chang, Ya-Nan, Chen, Kui, Bai, Xue, Yu, Lai, Li, Juan, Li, Shan, Xing, Gengmei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5127043/
https://www.ncbi.nlm.nih.gov/pubmed/27899122
http://dx.doi.org/10.1186/s12989-016-0173-1
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author Xia, Lin
Gu, Weihong
Zhang, Mingyi
Chang, Ya-Nan
Chen, Kui
Bai, Xue
Yu, Lai
Li, Juan
Li, Shan
Xing, Gengmei
author_facet Xia, Lin
Gu, Weihong
Zhang, Mingyi
Chang, Ya-Nan
Chen, Kui
Bai, Xue
Yu, Lai
Li, Juan
Li, Shan
Xing, Gengmei
author_sort Xia, Lin
collection PubMed
description BACKGROUND: Nanotechnology developed rapidly in cellular diagnosis and treatment, the endocytic system was an important pathway for targeting cell. In the research of developing macrophages as drug carriers or important therapeutic targets, an interesting phenomenon, internalized nanoparticles induced to form binucleated macrophages, was found although the particles dose did not cause obvious cytotoxicity. RESULTS: Under 25 μg/ml, internalized 30 nm polystyrene beads(30 nm Ps nanoparticles) induced the formation of binucleated macrophages when they entered into endosomes via the endocytic pathway. These internalized 30 nm Ps nanoparticles (25 μg/ml) and 30 nm Au-NPs (1.575 ng/ml) also induced markedly rise of binucleated cell rates in A549, HePG-2 and HCT116. This endosome, aggregated anionic polystyrene particles were dispersed and bound on inner membrane, was induced to form a large vesicle-like structure (LVLS). This phenomenon blocked transport of the particles from the endosome to lysosome and therefore restricted endosomal membrane trafficking through the transport vesicles. Early endosome antigen-1 and Ras-related protein-11 expressions were upregulated; however, the localized distributions of these pivotal proteins were altered. We hypothesized that these LVLS were held by the internalized and dispersed particles decreasing the amount of cell membrane available to support the completion of cytokinesis. In addition, altered distributions of pivotal proteins prevented transfer vesicles from fusion and hampered the separation of daughter cells. CONCLUSIONS: 30 nm Ps nanoparticles induced formation of LVLS, blocked the vesicle transport in endocytic system and the distributions of regular proteins required in cytokinesis which led to binucleated cells of macrophages. Markedly raised binucleated rate was also observed in human lung adenocarcinoma epithelial cell line(A549), human hepatoma cell line(HePG-2) and human colorectal cancer cell line(HCT116) treated by 30 nm Ps nanoparticles and Au-NPs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12989-016-0173-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-51270432016-12-08 Endocytosed nanoparticles hold endosomes and stimulate binucleated cells formation Xia, Lin Gu, Weihong Zhang, Mingyi Chang, Ya-Nan Chen, Kui Bai, Xue Yu, Lai Li, Juan Li, Shan Xing, Gengmei Part Fibre Toxicol Research BACKGROUND: Nanotechnology developed rapidly in cellular diagnosis and treatment, the endocytic system was an important pathway for targeting cell. In the research of developing macrophages as drug carriers or important therapeutic targets, an interesting phenomenon, internalized nanoparticles induced to form binucleated macrophages, was found although the particles dose did not cause obvious cytotoxicity. RESULTS: Under 25 μg/ml, internalized 30 nm polystyrene beads(30 nm Ps nanoparticles) induced the formation of binucleated macrophages when they entered into endosomes via the endocytic pathway. These internalized 30 nm Ps nanoparticles (25 μg/ml) and 30 nm Au-NPs (1.575 ng/ml) also induced markedly rise of binucleated cell rates in A549, HePG-2 and HCT116. This endosome, aggregated anionic polystyrene particles were dispersed and bound on inner membrane, was induced to form a large vesicle-like structure (LVLS). This phenomenon blocked transport of the particles from the endosome to lysosome and therefore restricted endosomal membrane trafficking through the transport vesicles. Early endosome antigen-1 and Ras-related protein-11 expressions were upregulated; however, the localized distributions of these pivotal proteins were altered. We hypothesized that these LVLS were held by the internalized and dispersed particles decreasing the amount of cell membrane available to support the completion of cytokinesis. In addition, altered distributions of pivotal proteins prevented transfer vesicles from fusion and hampered the separation of daughter cells. CONCLUSIONS: 30 nm Ps nanoparticles induced formation of LVLS, blocked the vesicle transport in endocytic system and the distributions of regular proteins required in cytokinesis which led to binucleated cells of macrophages. Markedly raised binucleated rate was also observed in human lung adenocarcinoma epithelial cell line(A549), human hepatoma cell line(HePG-2) and human colorectal cancer cell line(HCT116) treated by 30 nm Ps nanoparticles and Au-NPs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12989-016-0173-1) contains supplementary material, which is available to authorized users. BioMed Central 2016-11-29 /pmc/articles/PMC5127043/ /pubmed/27899122 http://dx.doi.org/10.1186/s12989-016-0173-1 Text en © The Author(s). 2016 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Xia, Lin
Gu, Weihong
Zhang, Mingyi
Chang, Ya-Nan
Chen, Kui
Bai, Xue
Yu, Lai
Li, Juan
Li, Shan
Xing, Gengmei
Endocytosed nanoparticles hold endosomes and stimulate binucleated cells formation
title Endocytosed nanoparticles hold endosomes and stimulate binucleated cells formation
title_full Endocytosed nanoparticles hold endosomes and stimulate binucleated cells formation
title_fullStr Endocytosed nanoparticles hold endosomes and stimulate binucleated cells formation
title_full_unstemmed Endocytosed nanoparticles hold endosomes and stimulate binucleated cells formation
title_short Endocytosed nanoparticles hold endosomes and stimulate binucleated cells formation
title_sort endocytosed nanoparticles hold endosomes and stimulate binucleated cells formation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5127043/
https://www.ncbi.nlm.nih.gov/pubmed/27899122
http://dx.doi.org/10.1186/s12989-016-0173-1
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