Detection of large extracellular silver nanoparticle rings observed during mitosis using darkfield microscopy.
Robert M ZuckerJayna OrtenzioLaura L DegnWilliam K BoyesPublished in: PloS one (2020)
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.
Keyphrases
- silver nanoparticles
- induced apoptosis
- high resolution
- label free
- cell cycle arrest
- endothelial cells
- single molecule
- cell cycle
- photodynamic therapy
- high throughput
- high speed
- endoplasmic reticulum stress
- quantum dots
- walled carbon nanotubes
- single cell
- stem cells
- escherichia coli
- signaling pathway
- cell death
- pseudomonas aeruginosa
- cystic fibrosis
- bone marrow
- diffusion weighted imaging
- induced pluripotent stem cells
- cell migration