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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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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. |
format | Online Article Text |
id | pubmed-5127043 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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