Automated cell identification and tracking using nanoparticle moving-light-displays.

An automated technique for the identification, tracking and analysis of biological cells is presented. It is based on the use of nanoparticles, enclosed within intra-cellular vesicles, to produce clusters of discrete, point-like fluorescent, light sources within the cells. Computational analysis of...

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Main Authors: James A Tonkin, Paul Rees, Martyn R Brown, Rachel J Errington, Paul J Smith, Sally C Chappell, Huw D Summers
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22829889/pdf/?tool=EBI
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spelling doaj-9eca5d7beb7146dcb8f31eeb9942ddd42021-03-03T20:28:19ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0177e4083510.1371/journal.pone.0040835Automated cell identification and tracking using nanoparticle moving-light-displays.James A TonkinPaul ReesMartyn R BrownRachel J ErringtonPaul J SmithSally C ChappellHuw D SummersAn automated technique for the identification, tracking and analysis of biological cells is presented. It is based on the use of nanoparticles, enclosed within intra-cellular vesicles, to produce clusters of discrete, point-like fluorescent, light sources within the cells. Computational analysis of these light ensembles in successive time frames of a movie sequence, using k-means clustering and particle tracking algorithms, provides robust and automated discrimination of live cells and their motion and a quantitative measure of their proliferation. This approach is a cytometric version of the moving light display technique which is widely used for analyzing the biological motion of humans and animals. We use the endocytosis of CdTe/ZnS, core-shell quantum dots to produce the light displays within an A549, epithelial, lung cancer cell line, using time-lapse imaging with frame acquisition every 5 minutes over a 40 hour time period. The nanoparticle moving light displays provide simultaneous collection of cell motility data, resolution of mitotic traversal dynamics and identification of familial relationships allowing construction of multi-parameter lineage trees.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22829889/pdf/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author James A Tonkin
Paul Rees
Martyn R Brown
Rachel J Errington
Paul J Smith
Sally C Chappell
Huw D Summers
spellingShingle James A Tonkin
Paul Rees
Martyn R Brown
Rachel J Errington
Paul J Smith
Sally C Chappell
Huw D Summers
Automated cell identification and tracking using nanoparticle moving-light-displays.
PLoS ONE
author_facet James A Tonkin
Paul Rees
Martyn R Brown
Rachel J Errington
Paul J Smith
Sally C Chappell
Huw D Summers
author_sort James A Tonkin
title Automated cell identification and tracking using nanoparticle moving-light-displays.
title_short Automated cell identification and tracking using nanoparticle moving-light-displays.
title_full Automated cell identification and tracking using nanoparticle moving-light-displays.
title_fullStr Automated cell identification and tracking using nanoparticle moving-light-displays.
title_full_unstemmed Automated cell identification and tracking using nanoparticle moving-light-displays.
title_sort automated cell identification and tracking using nanoparticle moving-light-displays.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description An automated technique for the identification, tracking and analysis of biological cells is presented. It is based on the use of nanoparticles, enclosed within intra-cellular vesicles, to produce clusters of discrete, point-like fluorescent, light sources within the cells. Computational analysis of these light ensembles in successive time frames of a movie sequence, using k-means clustering and particle tracking algorithms, provides robust and automated discrimination of live cells and their motion and a quantitative measure of their proliferation. This approach is a cytometric version of the moving light display technique which is widely used for analyzing the biological motion of humans and animals. We use the endocytosis of CdTe/ZnS, core-shell quantum dots to produce the light displays within an A549, epithelial, lung cancer cell line, using time-lapse imaging with frame acquisition every 5 minutes over a 40 hour time period. The nanoparticle moving light displays provide simultaneous collection of cell motility data, resolution of mitotic traversal dynamics and identification of familial relationships allowing construction of multi-parameter lineage trees.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22829889/pdf/?tool=EBI
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AT sallycchappell automatedcellidentificationandtrackingusingnanoparticlemovinglightdisplays
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