Cargando…

Systematic dielectrophoretic analysis of the Ara-C-induced NB4 cell apoptosis combined with gene expression profiling

Dielectrophoresis (DEP) can be used to noninvasively measure the dielectric state of the cell, and this data can be used to monitor cell health or apoptosis. In this study, we followed events associated with cytosine arabinoside (Ara-C)-induced apoptosis in NB4 cells using DEP analysis. Our data sho...

Descripción completa

Detalles Bibliográficos
Autores principales: Lv, Yi, Zeng, Lingqin, Zhang, Guanbin, Xu, Youchun, Lu, Ying, Mitchelson, Keith, Cheng, Jing, Xing, Wanli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3700913/
https://www.ncbi.nlm.nih.gov/pubmed/23847416
http://dx.doi.org/10.2147/IJN.S31678
_version_ 1782275559271694336
author Lv, Yi
Zeng, Lingqin
Zhang, Guanbin
Xu, Youchun
Lu, Ying
Mitchelson, Keith
Cheng, Jing
Xing, Wanli
author_facet Lv, Yi
Zeng, Lingqin
Zhang, Guanbin
Xu, Youchun
Lu, Ying
Mitchelson, Keith
Cheng, Jing
Xing, Wanli
author_sort Lv, Yi
collection PubMed
description Dielectrophoresis (DEP) can be used to noninvasively measure the dielectric state of the cell, and this data can be used to monitor cell health or apoptosis. In this study, we followed events associated with cytosine arabinoside (Ara-C)-induced apoptosis in NB4 cells using DEP analysis. Our data showed that the membrane capacitance of NB4 cells decreases from 9.42 to 7.63 mF/m(2) in the first 2 hours following treatment with Ara-C, and that this decreased capacitance persists for >12 hours. Additionally, cytoplasmic conductivity decreases from 0.217 to 0.190 S/m within 2 hours of Ara-C treatment; this level is maintained for a short period of time before decreasing. We also investigated these events molecularly at the level of gene expression using microarray analysis and showed that the expression of genes related to membrane capacitance and cytoplasmic conductivity change dramatically as early as 2 hours post-Ara-C treatment, and further demonstrated a temporal relationship between the dielectric properties and key events in apoptosis. This study, integrating physical electrical properties of the cell membrane and cytoplasm with those of conductivity-related gene networks, provides new insights into the molecular mechanisms underlying the initiation of apoptosis, establishing a systematic foundation for DEP application in follow-up drug screening and development of medicines for treating leukemia.
format Online
Article
Text
id pubmed-3700913
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Dove Medical Press
record_format MEDLINE/PubMed
spelling pubmed-37009132013-07-11 Systematic dielectrophoretic analysis of the Ara-C-induced NB4 cell apoptosis combined with gene expression profiling Lv, Yi Zeng, Lingqin Zhang, Guanbin Xu, Youchun Lu, Ying Mitchelson, Keith Cheng, Jing Xing, Wanli Int J Nanomedicine Original Research Dielectrophoresis (DEP) can be used to noninvasively measure the dielectric state of the cell, and this data can be used to monitor cell health or apoptosis. In this study, we followed events associated with cytosine arabinoside (Ara-C)-induced apoptosis in NB4 cells using DEP analysis. Our data showed that the membrane capacitance of NB4 cells decreases from 9.42 to 7.63 mF/m(2) in the first 2 hours following treatment with Ara-C, and that this decreased capacitance persists for >12 hours. Additionally, cytoplasmic conductivity decreases from 0.217 to 0.190 S/m within 2 hours of Ara-C treatment; this level is maintained for a short period of time before decreasing. We also investigated these events molecularly at the level of gene expression using microarray analysis and showed that the expression of genes related to membrane capacitance and cytoplasmic conductivity change dramatically as early as 2 hours post-Ara-C treatment, and further demonstrated a temporal relationship between the dielectric properties and key events in apoptosis. This study, integrating physical electrical properties of the cell membrane and cytoplasm with those of conductivity-related gene networks, provides new insights into the molecular mechanisms underlying the initiation of apoptosis, establishing a systematic foundation for DEP application in follow-up drug screening and development of medicines for treating leukemia. Dove Medical Press 2013 2013-06-28 /pmc/articles/PMC3700913/ /pubmed/23847416 http://dx.doi.org/10.2147/IJN.S31678 Text en © 2013 Lv et al, publisher and licensee Dove Medical Press Ltd This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Original Research
Lv, Yi
Zeng, Lingqin
Zhang, Guanbin
Xu, Youchun
Lu, Ying
Mitchelson, Keith
Cheng, Jing
Xing, Wanli
Systematic dielectrophoretic analysis of the Ara-C-induced NB4 cell apoptosis combined with gene expression profiling
title Systematic dielectrophoretic analysis of the Ara-C-induced NB4 cell apoptosis combined with gene expression profiling
title_full Systematic dielectrophoretic analysis of the Ara-C-induced NB4 cell apoptosis combined with gene expression profiling
title_fullStr Systematic dielectrophoretic analysis of the Ara-C-induced NB4 cell apoptosis combined with gene expression profiling
title_full_unstemmed Systematic dielectrophoretic analysis of the Ara-C-induced NB4 cell apoptosis combined with gene expression profiling
title_short Systematic dielectrophoretic analysis of the Ara-C-induced NB4 cell apoptosis combined with gene expression profiling
title_sort systematic dielectrophoretic analysis of the ara-c-induced nb4 cell apoptosis combined with gene expression profiling
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3700913/
https://www.ncbi.nlm.nih.gov/pubmed/23847416
http://dx.doi.org/10.2147/IJN.S31678
work_keys_str_mv AT lvyi systematicdielectrophoreticanalysisofthearacinducednb4cellapoptosiscombinedwithgeneexpressionprofiling
AT zenglingqin systematicdielectrophoreticanalysisofthearacinducednb4cellapoptosiscombinedwithgeneexpressionprofiling
AT zhangguanbin systematicdielectrophoreticanalysisofthearacinducednb4cellapoptosiscombinedwithgeneexpressionprofiling
AT xuyouchun systematicdielectrophoreticanalysisofthearacinducednb4cellapoptosiscombinedwithgeneexpressionprofiling
AT luying systematicdielectrophoreticanalysisofthearacinducednb4cellapoptosiscombinedwithgeneexpressionprofiling
AT mitchelsonkeith systematicdielectrophoreticanalysisofthearacinducednb4cellapoptosiscombinedwithgeneexpressionprofiling
AT chengjing systematicdielectrophoreticanalysisofthearacinducednb4cellapoptosiscombinedwithgeneexpressionprofiling
AT xingwanli systematicdielectrophoreticanalysisofthearacinducednb4cellapoptosiscombinedwithgeneexpressionprofiling