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Development of a novel, multi-analyte biosensor system for assaying cell division: Identification of cell proliferation/death precursor events

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dc.contributor.author Kintzios, S en
dc.contributor.author Marinopoulou, I en
dc.contributor.author Moschopoulou, G en
dc.contributor.author Mangana, O en
dc.contributor.author Nomikou, K en
dc.contributor.author Endo, K en
dc.contributor.author Papanastasiou, I en
dc.contributor.author Simonian, A en
dc.date.accessioned 2014-06-06T06:47:18Z
dc.date.available 2014-06-06T06:47:18Z
dc.date.issued 2006 en
dc.identifier.issn 09565663 en
dc.identifier.uri http://dx.doi.org/10.1016/j.bios.2005.04.022 en
dc.identifier.uri http://62.217.125.90/xmlui/handle/123456789/3510
dc.subject Bioelectric recognition assay (BERA) en
dc.subject Cell immobilization en
dc.subject Cell proliferation signal en
dc.subject Fluorescence microscopy en
dc.subject Oxidative stress en
dc.subject Superoxide dismutase en
dc.subject.other Bioassay en
dc.subject.other Bioelectric phenomena en
dc.subject.other Cell immobilization en
dc.subject.other Cells en
dc.subject.other Electrophysiology en
dc.subject.other Enzymes en
dc.subject.other Fluorescence en
dc.subject.other Optical microscopy en
dc.subject.other Oxidation en
dc.subject.other Bioelectric recognition assays (BERA) en
dc.subject.other Cell proliferation signals en
dc.subject.other Fluorescence microscopy en
dc.subject.other Oxidative stress en
dc.subject.other Superoxide dimutase en
dc.subject.other Biosensors en
dc.subject.other calcium alginate en
dc.subject.other glutathione en
dc.subject.other reactive oxygen metabolite en
dc.subject.other superoxide dismutase en
dc.subject.other article en
dc.subject.other biosensor en
dc.subject.other cell culture en
dc.subject.other cell death en
dc.subject.other cell division en
dc.subject.other cell function en
dc.subject.other cell membrane potential en
dc.subject.other cell proliferation en
dc.subject.other cell viability en
dc.subject.other concentration (parameters) en
dc.subject.other correlation analysis en
dc.subject.other electrode en
dc.subject.other electrophysiology en
dc.subject.other fluorescence microscopy en
dc.subject.other measurement en
dc.subject.other microscopy en
dc.subject.other technology en
dc.subject.other Animals en
dc.subject.other Apoptosis en
dc.subject.other Biosensing Techniques en
dc.subject.other Cell Culture Techniques en
dc.subject.other Cell Division en
dc.subject.other Cells, Immobilized en
dc.subject.other Cercopithecus aethiops en
dc.subject.other Electrochemistry en
dc.subject.other Equipment Design en
dc.subject.other Equipment Failure Analysis en
dc.subject.other Membrane Potentials en
dc.subject.other Microfluidic Analytical Techniques en
dc.subject.other Oxidative Stress en
dc.subject.other Reactive Oxygen Species en
dc.subject.other Superoxide Dismutase en
dc.subject.other Systems Integration en
dc.subject.other Vero Cells en
dc.title Development of a novel, multi-analyte biosensor system for assaying cell division: Identification of cell proliferation/death precursor events en
heal.type journalArticle en
heal.identifier.primary 10.1016/j.bios.2005.04.022 en
heal.publicationDate 2006 en
heal.abstract A novel, miniaturized biosensor system was created by combining the electrophysiological response of immobilized cells with superoxide-sensing technology, optical and fluorescence microscopy. Vero cells were immobilized in a calcium alginate matrix (at a density of 1.7 × 10 6 cells ml -1). A 0.5 cm × 0.5 cm piece of cell-containing gel matrix was aseptically adhered on a glass microscope slide with a microfabricated gold electrode array, sealed with a cover slip and provided with Dulbecco's medium +10% (v/v) fetal calf serum every day by means of a capillary feeding tube. During a culture period of 7 days, the membrane potential of immobilized cells was continuously monitored, while cell division was assayed with an optical microscope. In addition, daily measurements of immobilized cell membrane potential, viability, RNA and calcium concentration, radical oxygen species (ROS) and glutathione accumulation, were conducted by fluorescence microscopy after provision of an appropriate dye. Superoxide accumulation was assayed by covering the electrodes with superoxide dismutase (SOD). Maximum cell membrane potential values and superoxide production were observed upon initiation of cell division. Using the novel biosensor, we were able to correlate seven different cell physiological parameters to each other and formulate a model for ROS-mediated signaling function on cell division and death. In addition, we were able to predict cell proliferation or death by comparing the relative response of the electrophysiological and superoxide sensor during the culture period. © 2005 Elsevier B.V. All rights reserved. en
heal.journalName Biosensors and Bioelectronics en
dc.identifier.issue 7 en
dc.identifier.volume 21 en
dc.identifier.doi 10.1016/j.bios.2005.04.022 en
dc.identifier.spage 1365 en
dc.identifier.epage 1373 en


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