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Rapid assessment of early biophysical changes in K562 cells during apoptosis determined using dielectrophoresis
Apoptosis, or programmed cell death, is a vital cellular process responsible for causing cells to self-terminate at the end of their useful life. Abrogation of this process is commonly linked to cancer, and rapid detection of apoptosis in vitro is vital to the discovery of new anti-cancer drugs. In...
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Formato: | Texto |
Lenguaje: | English |
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Dove Medical Press
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2426800/ https://www.ncbi.nlm.nih.gov/pubmed/17717973 |
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author | Chin, Sue Hughes, Michael P Coley, Helen M Labeed, Fatima H |
author_facet | Chin, Sue Hughes, Michael P Coley, Helen M Labeed, Fatima H |
author_sort | Chin, Sue |
collection | PubMed |
description | Apoptosis, or programmed cell death, is a vital cellular process responsible for causing cells to self-terminate at the end of their useful life. Abrogation of this process is commonly linked to cancer, and rapid detection of apoptosis in vitro is vital to the discovery of new anti-cancer drugs. In this paper, we describe the application of the electrical phenomenon dielectrophoresis for detecting apoptosis at very early stages after drug induction, on the basis of changes in electrophysiological properties. Our studies have revealed that K562 (human myelogenous leukemia) cells show a persistent elevation in the cytoplasmic conductivity occurring as early as 30 minutes following exposure to staurosporine. This method therefore allows a far more rapid detection method than existing biochemical marker methods. |
format | Text |
id | pubmed-2426800 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-24268002008-06-20 Rapid assessment of early biophysical changes in K562 cells during apoptosis determined using dielectrophoresis Chin, Sue Hughes, Michael P Coley, Helen M Labeed, Fatima H Int J Nanomedicine Original Research Apoptosis, or programmed cell death, is a vital cellular process responsible for causing cells to self-terminate at the end of their useful life. Abrogation of this process is commonly linked to cancer, and rapid detection of apoptosis in vitro is vital to the discovery of new anti-cancer drugs. In this paper, we describe the application of the electrical phenomenon dielectrophoresis for detecting apoptosis at very early stages after drug induction, on the basis of changes in electrophysiological properties. Our studies have revealed that K562 (human myelogenous leukemia) cells show a persistent elevation in the cytoplasmic conductivity occurring as early as 30 minutes following exposure to staurosporine. This method therefore allows a far more rapid detection method than existing biochemical marker methods. Dove Medical Press 2006-09 /pmc/articles/PMC2426800/ /pubmed/17717973 Text en © 2006 Dove Medical Press Limited. All rights reserved |
spellingShingle | Original Research Chin, Sue Hughes, Michael P Coley, Helen M Labeed, Fatima H Rapid assessment of early biophysical changes in K562 cells during apoptosis determined using dielectrophoresis |
title | Rapid assessment of early biophysical changes in K562 cells during apoptosis determined using dielectrophoresis |
title_full | Rapid assessment of early biophysical changes in K562 cells during apoptosis determined using dielectrophoresis |
title_fullStr | Rapid assessment of early biophysical changes in K562 cells during apoptosis determined using dielectrophoresis |
title_full_unstemmed | Rapid assessment of early biophysical changes in K562 cells during apoptosis determined using dielectrophoresis |
title_short | Rapid assessment of early biophysical changes in K562 cells during apoptosis determined using dielectrophoresis |
title_sort | rapid assessment of early biophysical changes in k562 cells during apoptosis determined using dielectrophoresis |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2426800/ https://www.ncbi.nlm.nih.gov/pubmed/17717973 |
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