Publication:
Scanning electrochemical microscopy of model neurons: Imaging and real-time detection of morphological changes

dc.contributor.authorLiebetrau J.M.
dc.contributor.authorMiller H.M.
dc.contributor.authorBaur J.E.
dc.contributor.authorTakacs S.A.
dc.contributor.authorAnupunpisit V.
dc.contributor.authorGarris P.A.
dc.contributor.authorWipf D.O.
dc.date.accessioned2021-04-05T04:32:55Z
dc.date.available2021-04-05T04:32:55Z
dc.date.issued2003
dc.date.issuedBE2546
dc.description.abstractLiving PC12 cells, a model cell type for studying neuronal function, were imaged using the negative feedback mode of a scanning electrochemical microscope (SECM). Six biocompatible redox mediators were successfully identified from a large pool of candidates and were then used for imaging PC12 cells before and after exposure to nerve growth factor (NGF). When exposed to NGF, cells differentiate into a neuron phenotype by growing narrow neurites (1-2 μm wide) that can extend >100 μm from the cell proper. We demonstrate that carbon fiber electrodes with reduced tip diameters can be used for imaging both the cell proper and these neurites. Regions of decreased current, possibly resulting from raised features not identifiable by light microscopy, are clearly evident in the SECM images. Changes in the morphology of undifferentiated PC12 cells could be detected in real time with the SECM. After exposure to hypotonic and hypertonic solutions, reversible changes in cell height of <2 μm were measured.
dc.format.mimetypeapplication/pdf
dc.identifier.citationAnalytical Chemistry. Vol 75, No.3 (2003), p.563-571
dc.identifier.doi10.1021/ac026166v
dc.identifier.issn32700
dc.identifier.other2-s2.0-0037312636
dc.identifier.urihttps://swu-dspace2.eval.plus/handle/123456789/6593
dc.rights.holderScopus
dc.subject.otherBiocompatibility
dc.subject.otherCarbon fibers
dc.subject.otherCells
dc.subject.otherImaging techniques
dc.subject.otherMicroscopic examination
dc.subject.otherMorphology
dc.subject.otherNeurology
dc.subject.otherScanning electrochemical microscopy (SECM)
dc.subject.otherElectrochemistry
dc.subject.otherDopamine
dc.subject.otherAnimal cell
dc.subject.otherArticle
dc.subject.otherCell strain
dc.subject.otherCell structure
dc.subject.otherCell type
dc.subject.otherCyclic potentiometry
dc.subject.otherDopamine release
dc.subject.otherElectrochemical analysis
dc.subject.otherElectrode
dc.subject.otherHigh performance liquid chromatography
dc.subject.otherMicroscopy
dc.subject.otherModel
dc.subject.otherMorphology
dc.subject.otherNerve cell
dc.subject.otherNerve cell differentiation
dc.subject.otherNeurotransmitter release
dc.subject.otherNonhuman
dc.subject.otherRat
dc.subject.otherScanning electrochemical microscopy
dc.subject.otherScanning electron microscopy
dc.subject.otherAnimals
dc.subject.otherDiagnostic Imaging
dc.subject.otherElectrochemistry
dc.subject.otherMicroelectrodes
dc.subject.otherMicroscopy, Electron, Scanning
dc.subject.otherNerve Growth Factor
dc.subject.otherNeurons
dc.subject.otherPC12 Cells
dc.subject.otherRats
dc.titleScanning electrochemical microscopy of model neurons: Imaging and real-time detection of morphological changes
dc.typeArticle
dspace.entity.typePublication
swu.datasource.scopushttps://www.scopus.com/inward/record.uri?eid=2-s2.0-0037312636&doi=10.1021%2fac026166v&partnerID=40&md5=6b9b86bf7069cd6c12771cc5a650dc9f

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