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Label-free imaging of membrane potential using membrane electromotility

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dc.contributor.authorOh, S.-
dc.contributor.authorFang-Yen, C.-
dc.contributor.authorChoi, W.-
dc.contributor.authorYaqoob, Z.-
dc.contributor.authorFu, D.-
dc.contributor.authorPark, Y.-
dc.contributor.authorDassari, R.R.-
dc.contributor.authorFeld, M.S.-
dc.date.accessioned2021-09-07T04:08:56Z-
dc.date.available2021-09-07T04:08:56Z-
dc.date.created2021-06-17-
dc.date.issued2012-
dc.identifier.issn0006-3495-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/110641-
dc.description.abstractElectrical activity may cause observable changes in a cell's structure in the absence of exogenous reporter molecules. In this work, we report a low-coherence interferometric microscopy technique that can detect an optical signal correlated with the membrane potential changes in individual mammalian cells without exogenous labels. By measuring milliradian-scale phase shifts in the transmitted light, we can detect changes in the cells' membrane potential. We find that the observed optical signals are due to membrane electromotility, which causes the cells to deform in response to the membrane potential changes. We demonstrate wide-field imaging of the propagation of electrical stimuli in gap-junction-coupled cell networks. Membrane electromotility-induced cell deformation may be useful as a reporter of electrical activity. © 2012 Biophysical Society.-
dc.languageEnglish-
dc.language.isoen-
dc.subjectaction potential-
dc.subjectarticle-
dc.subjectcell membrane-
dc.subjectcell strain HEK293-
dc.subjectelectrical synapse-
dc.subjecthuman-
dc.subjectlight related phenomena-
dc.subjectmolecular imaging-
dc.subjectpatch clamp-
dc.subjectphase contrast microscopy-
dc.subjectphysiology-
dc.subjectultrastructure-
dc.subjectAction Potentials-
dc.subjectCell Membrane-
dc.subjectElectrical Synapses-
dc.subjectHEK293 Cells-
dc.subjectHumans-
dc.subjectMicroscopy, Interference-
dc.subjectMolecular Imaging-
dc.subjectOptical Processes-
dc.subjectPatch-Clamp Techniques-
dc.subjectMammalia-
dc.titleLabel-free imaging of membrane potential using membrane electromotility-
dc.typeArticle-
dc.contributor.affiliatedAuthorFang-Yen, C.-
dc.contributor.affiliatedAuthorChoi, W.-
dc.identifier.doi10.1016/j.bpj.2012.05.020-
dc.identifier.scopusid2-s2.0-84863484151-
dc.identifier.bibliographicCitationBiophysical Journal, v.103, no.1, pp.11 - 18-
dc.relation.isPartOfBiophysical Journal-
dc.citation.titleBiophysical Journal-
dc.citation.volume103-
dc.citation.number1-
dc.citation.startPage11-
dc.citation.endPage18-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.subject.keywordPlusaction potential-
dc.subject.keywordPlusarticle-
dc.subject.keywordPluscell membrane-
dc.subject.keywordPluscell strain HEK293-
dc.subject.keywordPluselectrical synapse-
dc.subject.keywordPlushuman-
dc.subject.keywordPluslight related phenomena-
dc.subject.keywordPlusmolecular imaging-
dc.subject.keywordPluspatch clamp-
dc.subject.keywordPlusphase contrast microscopy-
dc.subject.keywordPlusphysiology-
dc.subject.keywordPlusultrastructure-
dc.subject.keywordPlusAction Potentials-
dc.subject.keywordPlusCell Membrane-
dc.subject.keywordPlusElectrical Synapses-
dc.subject.keywordPlusHEK293 Cells-
dc.subject.keywordPlusHumans-
dc.subject.keywordPlusMicroscopy, Interference-
dc.subject.keywordPlusMolecular Imaging-
dc.subject.keywordPlusOptical Processes-
dc.subject.keywordPlusPatch-Clamp Techniques-
dc.subject.keywordPlusMammalia-
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