Detection of cellular responses to toxicants by dielectrophoresis

The dielectrophoretic (DEP) crossover method has been applied to the detection of cell responses to toxicants. Time and dose responses of the human cultured leukemia (HL-60) line were measured for paraquat, styrene oxide (SO), N-nitroso-N-methylurea (NMU) and puromycin. These toxicants were chosen b...

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Main Authors: Kanatip Ratanachoo, Peter R.C. Gascoyne, Mathuros Ruchirawat
Other Authors: Chulabhorn Research Institute
Format: Article
Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/20049
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spelling th-mahidol.200492018-07-24T09:56:32Z Detection of cellular responses to toxicants by dielectrophoresis Kanatip Ratanachoo Peter R.C. Gascoyne Mathuros Ruchirawat Chulabhorn Research Institute University of Texas MD Anderson Cancer Center Mahidol University Biochemistry, Genetics and Molecular Biology The dielectrophoretic (DEP) crossover method has been applied to the detection of cell responses to toxicants. Time and dose responses of the human cultured leukemia (HL-60) line were measured for paraquat, styrene oxide (SO), N-nitroso-N-methylurea (NMU) and puromycin. These toxicants were chosen because of their different predominant mechanisms of action, namely membrane free radical attack, simultaneous membrane and nucleic acid attack, nucleic acid alkylation, and protein synthesis inhibition, respectively. For all treatments, the specific membrane capacitance (Cmem) of the cells decreased while the specific membrane conductance (Gmem) increased in dose- and time-dependent manners. The DEP responses correlated sensitively with alterations in cell surface morphology, especially folds, microvilli, and blebs, observed by scanning electron microscopy. The DEP method was more sensitive to agents that had a direct action on the membrane than to agents for which membrane alterations were secondary. The responses to paraquat and SO, which directly damaged the cell membrane, could be detected 15 min after exposure, while those for puromycin and NMU, which acted on intracellular targets, could be detected after 30 min. The detection times and dose sensitivity results showed that the DEP method is much faster and more sensitive than conventional cell and higher organism viability testing techniques. The feasibility of producing small instruments for toxicity detection and screening based on cellular dielectric responses is discussed. © 2002 Elsevier Science B.V. All rights reserved. 2018-07-24T02:56:32Z 2018-07-24T02:56:32Z 2002-08-31 Article Biochimica et Biophysica Acta - Biomembranes. Vol.1564, No.2 (2002), 449-458 10.1016/S0005-2736(02)00494-7 00052736 2-s2.0-0037206163 https://repository.li.mahidol.ac.th/handle/123456789/20049 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0037206163&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Biochemistry, Genetics and Molecular Biology
spellingShingle Biochemistry, Genetics and Molecular Biology
Kanatip Ratanachoo
Peter R.C. Gascoyne
Mathuros Ruchirawat
Detection of cellular responses to toxicants by dielectrophoresis
description The dielectrophoretic (DEP) crossover method has been applied to the detection of cell responses to toxicants. Time and dose responses of the human cultured leukemia (HL-60) line were measured for paraquat, styrene oxide (SO), N-nitroso-N-methylurea (NMU) and puromycin. These toxicants were chosen because of their different predominant mechanisms of action, namely membrane free radical attack, simultaneous membrane and nucleic acid attack, nucleic acid alkylation, and protein synthesis inhibition, respectively. For all treatments, the specific membrane capacitance (Cmem) of the cells decreased while the specific membrane conductance (Gmem) increased in dose- and time-dependent manners. The DEP responses correlated sensitively with alterations in cell surface morphology, especially folds, microvilli, and blebs, observed by scanning electron microscopy. The DEP method was more sensitive to agents that had a direct action on the membrane than to agents for which membrane alterations were secondary. The responses to paraquat and SO, which directly damaged the cell membrane, could be detected 15 min after exposure, while those for puromycin and NMU, which acted on intracellular targets, could be detected after 30 min. The detection times and dose sensitivity results showed that the DEP method is much faster and more sensitive than conventional cell and higher organism viability testing techniques. The feasibility of producing small instruments for toxicity detection and screening based on cellular dielectric responses is discussed. © 2002 Elsevier Science B.V. All rights reserved.
author2 Chulabhorn Research Institute
author_facet Chulabhorn Research Institute
Kanatip Ratanachoo
Peter R.C. Gascoyne
Mathuros Ruchirawat
format Article
author Kanatip Ratanachoo
Peter R.C. Gascoyne
Mathuros Ruchirawat
author_sort Kanatip Ratanachoo
title Detection of cellular responses to toxicants by dielectrophoresis
title_short Detection of cellular responses to toxicants by dielectrophoresis
title_full Detection of cellular responses to toxicants by dielectrophoresis
title_fullStr Detection of cellular responses to toxicants by dielectrophoresis
title_full_unstemmed Detection of cellular responses to toxicants by dielectrophoresis
title_sort detection of cellular responses to toxicants by dielectrophoresis
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/20049
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