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Endocytosed nanoparticles hold endosomes and stimulate binucleated cells formation

文献类型：期刊论文

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作者Xia L(夏林); Gu WH(古伟宏); Zhang MY(张铭倚); Chang YN(常亚男); Chen K(陈奎); Bai X(白雪); Li J(李娟); Li S(李珊); Xing GM(邢更妹); Xia, L
刊名PARTICLE AND FIBRE TOXICOLOGY ; PARTICLE AND FIBRE TOXICOLOGY
出版日期2016 ; 2016
卷号13页码:-
关键词Nanoparticles Nanoparticles Endocytic Endosome Large vesicle-like structures Binucleated cell Endocytic Endosome Large vesicle-like structures Binucleated cell
ISSN号1743-8977
DOI10.1186/s12989-016-0173-1 ; 10.1186/s12989-016-0173-1
通讯作者李珊 ; 李珊 ; 邢更妹 ; 邢更妹
文献子类Article
英文摘要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 mu g/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 mu g/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.; 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 mu g/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 mu g/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.
WOS关键词RECYCLING ENDOSOME ; CLEAVAGE FURROW ; LATE MITOSIS ; CYTOKINESIS ; BINDING ; MECHANISM ; PROTEIN ; GOLGI ; EEA1
语种英语 ; 英语
WOS记录号WOS:000389782600001 ; WOS:000389782600001
源URL[http://ir.ihep.ac.cn/handle/311005/260480]  
专题高能物理研究所_多学科研究中心
作者单位中国科学院高能物理研究所
推荐引用方式
GB/T 7714		 Xia L,Gu WH,Zhang MY,et al. Endocytosed nanoparticles hold endosomes and stimulate binucleated cells formation, Endocytosed nanoparticles hold endosomes and stimulate binucleated cells formation[J]. PARTICLE AND FIBRE TOXICOLOGY, PARTICLE AND FIBRE TOXICOLOGY,2016, 2016,13, 13:-, 63.
APA 夏林.,古伟宏.,张铭倚.,常亚男.,陈奎.,...&Xing, GM.(2016).Endocytosed nanoparticles hold endosomes and stimulate binucleated cells formation.PARTICLE AND FIBRE TOXICOLOGY,13,-.
MLA 夏林,et al."Endocytosed nanoparticles hold endosomes and stimulate binucleated cells formation".PARTICLE AND FIBRE TOXICOLOGY 13(2016):-.

入库方式： OAI收割

来源：高能物理研究所

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