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Detection of large extracellular silver nanoparticle rings observed during mitosis using darkfield microscopy
During studies on the absorption and interactions between silver nanoparticles and mammalian cells grown in vitro it was observed that large extracellular rings of silver nanoparticles were deposited on the microscope slide, many located near post-mitotic cells. Silver nanoparticles (AgNP, 80nm), co...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7707489/ https://www.ncbi.nlm.nih.gov/pubmed/33259485 http://dx.doi.org/10.1371/journal.pone.0240268 |
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author | Zucker, Robert M. Ortenzio, Jayna Degn, Laura L. Boyes, William K. |
author_facet | Zucker, Robert M. Ortenzio, Jayna Degn, Laura L. Boyes, William K. |
author_sort | Zucker, Robert M. |
collection | PubMed |
description | During studies on the absorption and interactions between silver nanoparticles and mammalian cells grown in vitro it was observed that large extracellular rings of silver nanoparticles were deposited on the microscope slide, many located near post-mitotic cells. Silver nanoparticles (AgNP, 80nm), coated with citrate, were incubated at concentrations of 0.3 to 30 μg/ml with a human-derived culture of retinal pigment epithelial cells (ARPE-19) and observed using darkfield and fluorescent microscopy, 24 h after treatment. Approximately cell-sized extracellular rings of deposited AgNP were observed on the slides among a field of dispersed individual AgNP. The mean diameter of 45 nanoparticles circles was 62.5 +/-12 microns. Ring structures were frequently observed near what appeared to be post-mitotic daughter cells, giving rise to the possibility that cell membrane fragments were deposited on the slide during mitosis, and those fragments selectively attracted and retained silver nanoparticles from suspension in the cell culture medium. These circular structures were observable for the following technical reasons: 1) darkfield microscope could observe single nanoparticles below 100 nm in size, 2) a large concentration (10(8) and 10(9)) of nanoparticles was used in these experiments 3) negatively charged nanoparticles were attracted to adhesion membrane proteins remaining on the slide from mitosis. The observation of silver nanoparticles attracted to apparent remnants of cellular mitosis could be a useful tool for the study of normal and abnormal mitosis. |
format | Online Article Text |
id | pubmed-7707489 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-77074892020-12-08 Detection of large extracellular silver nanoparticle rings observed during mitosis using darkfield microscopy Zucker, Robert M. Ortenzio, Jayna Degn, Laura L. Boyes, William K. PLoS One Research Article During studies on the absorption and interactions between silver nanoparticles and mammalian cells grown in vitro it was observed that large extracellular rings of silver nanoparticles were deposited on the microscope slide, many located near post-mitotic cells. Silver nanoparticles (AgNP, 80nm), coated with citrate, were incubated at concentrations of 0.3 to 30 μg/ml with a human-derived culture of retinal pigment epithelial cells (ARPE-19) and observed using darkfield and fluorescent microscopy, 24 h after treatment. Approximately cell-sized extracellular rings of deposited AgNP were observed on the slides among a field of dispersed individual AgNP. The mean diameter of 45 nanoparticles circles was 62.5 +/-12 microns. Ring structures were frequently observed near what appeared to be post-mitotic daughter cells, giving rise to the possibility that cell membrane fragments were deposited on the slide during mitosis, and those fragments selectively attracted and retained silver nanoparticles from suspension in the cell culture medium. These circular structures were observable for the following technical reasons: 1) darkfield microscope could observe single nanoparticles below 100 nm in size, 2) a large concentration (10(8) and 10(9)) of nanoparticles was used in these experiments 3) negatively charged nanoparticles were attracted to adhesion membrane proteins remaining on the slide from mitosis. The observation of silver nanoparticles attracted to apparent remnants of cellular mitosis could be a useful tool for the study of normal and abnormal mitosis. Public Library of Science 2020-12-01 /pmc/articles/PMC7707489/ /pubmed/33259485 http://dx.doi.org/10.1371/journal.pone.0240268 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication. |
spellingShingle | Research Article Zucker, Robert M. Ortenzio, Jayna Degn, Laura L. Boyes, William K. Detection of large extracellular silver nanoparticle rings observed during mitosis using darkfield microscopy |
title | Detection of large extracellular silver nanoparticle rings observed during mitosis using darkfield microscopy |
title_full | Detection of large extracellular silver nanoparticle rings observed during mitosis using darkfield microscopy |
title_fullStr | Detection of large extracellular silver nanoparticle rings observed during mitosis using darkfield microscopy |
title_full_unstemmed | Detection of large extracellular silver nanoparticle rings observed during mitosis using darkfield microscopy |
title_short | Detection of large extracellular silver nanoparticle rings observed during mitosis using darkfield microscopy |
title_sort | detection of large extracellular silver nanoparticle rings observed during mitosis using darkfield microscopy |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7707489/ https://www.ncbi.nlm.nih.gov/pubmed/33259485 http://dx.doi.org/10.1371/journal.pone.0240268 |
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