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...

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Main Authors: Robert M Zucker, Jayna Ortenzio, Laura L Degn, William K Boyes
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2020-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0240268
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spelling doaj-4f4e712773af49309ebf8e7ed749190f2021-03-04T12:50:00ZengPublic Library of Science (PLoS)PLoS ONE1932-62032020-01-011512e024026810.1371/journal.pone.0240268Detection of large extracellular silver nanoparticle rings observed during mitosis using darkfield microscopy.Robert M ZuckerJayna OrtenzioLaura L DegnWilliam K BoyesDuring 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 (108 and 109) 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.https://doi.org/10.1371/journal.pone.0240268
collection DOAJ
language English
format Article
sources DOAJ
author Robert M Zucker
Jayna Ortenzio
Laura L Degn
William K Boyes
spellingShingle Robert M Zucker
Jayna Ortenzio
Laura L Degn
William K Boyes
Detection of large extracellular silver nanoparticle rings observed during mitosis using darkfield microscopy.
PLoS ONE
author_facet Robert M Zucker
Jayna Ortenzio
Laura L Degn
William K Boyes
author_sort Robert M Zucker
title 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_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_sort detection of large extracellular silver nanoparticle rings observed during mitosis using darkfield microscopy.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2020-01-01
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 (108 and 109) 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.
url https://doi.org/10.1371/journal.pone.0240268
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