Direct high-resolution label-free imaging of cellular nanostructure dynamics in living cells
DC Field | Value | Language |
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dc.contributor.author | Chaejeong Heo | - |
dc.contributor.author | Sohee Lee | - |
dc.contributor.author | Si Young Lee | - |
dc.contributor.author | Mun Seok Jeong | - |
dc.contributor.author | Lee, Young Hee | - |
dc.contributor.author | Minah Suh | - |
dc.date.available | 2015-04-20T06:57:36Z | - |
dc.date.created | 2014-08-11 | ko |
dc.date.issued | 2013-06 | - |
dc.identifier.issn | 1083-3668 | - |
dc.identifier.uri | https://pr.ibs.re.kr/handle/8788114/1318 | - |
dc.description.abstract | We report the application of an optical microscope equipped with a high-resolution dark-field condenser for detecting dynamic responses of cellular nanostructures in real time. Our system provides an easy-to-use technique to visualize biological specimens without any staining. This system can visualize the dynamic behavior of nanospheres and nanofibers, such as F-actin, at the leading edges of adjacent neuronal cells. We confirmed that the nanofibers imaged with this high-resolution optical microscopic technique are F-actin by using fluorescence microscopy after immunostaining the F-actin of fixed cells. Furthermore, cellular dynamics are enhanced by applying noncontact electric field stimulation through a transparent graphene electric field stimulator. High-resolution label-free optical microscopy enables the visualization of nanofiber dynamics initiated by filopodial nanofiber contacts. In conclusion, our optical microscopy system allows the visualization of nanoscale cellular dynamics under various external stimuli in real time without specific staining. (C) The Authors. Published by SPIE under a Creative Commons Attribution 3.0 Unported License. Distribution or reproduction of this work in whole or in part requires full attribution of the original publication, including its DOI. | - |
dc.language | 영어 | - |
dc.publisher | SPIE-SOC PHOTO-OPTICAL INSTRUMENTATION ENGINEERS | - |
dc.subject | high-resolution imaging | - |
dc.subject | live cell imaging | - |
dc.subject | F-actin | - |
dc.subject | label-free imaging | - |
dc.subject | electrical field stimulation | - |
dc.subject | graphene. | - |
dc.title | Direct high-resolution label-free imaging of cellular nanostructure dynamics in living cells | - |
dc.type | Article | - |
dc.type.rims | ART | - |
dc.identifier.wosid | 000322341100056 | - |
dc.identifier.scopusid | 2-s2.0-84879668223 | - |
dc.identifier.rimsid | 585 | ko |
dc.date.tcdate | 2018-10-01 | - |
dc.contributor.affiliatedAuthor | Chaejeong Heo | - |
dc.contributor.affiliatedAuthor | Si Young Lee | - |
dc.contributor.affiliatedAuthor | Mun Seok Jeong | - |
dc.contributor.affiliatedAuthor | Lee, Young Hee | - |
dc.identifier.doi | 10.1117/1.JBO.18.6.066016 | - |
dc.identifier.bibliographicCitation | JOURNAL OF BIOMEDICAL OPTICS, v.18, no.6, pp.66016 | - |
dc.relation.isPartOf | JOURNAL OF BIOMEDICAL OPTICS | - |
dc.citation.title | JOURNAL OF BIOMEDICAL OPTICS | - |
dc.citation.volume | 18 | - |
dc.citation.number | 6 | - |
dc.citation.startPage | 66016 | - |
dc.date.scptcdate | 2018-10-01 | - |
dc.description.scptc | 0 | - |
dc.description.journalClass | 1 | - |
dc.description.journalClass | 1 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.subject.keywordPlus | NEURITE GROWTH | - |
dc.subject.keywordPlus | MICROSCOPY | - |
dc.subject.keywordPlus | RECONSTRUCTION | - |
dc.subject.keywordPlus | POPULATIONS | - |
dc.subject.keywordPlus | FILOPODIA | - |
dc.subject.keywordPlus | TRANSPORT | - |
dc.subject.keywordPlus | EXPOSURE | - |
dc.subject.keywordPlus | NEURONS | - |
dc.subject.keywordPlus | NM | - |
dc.subject.keywordAuthor | high-resolution imaging | - |
dc.subject.keywordAuthor | live cell imaging | - |
dc.subject.keywordAuthor | F-actin | - |
dc.subject.keywordAuthor | label-free imaging | - |
dc.subject.keywordAuthor | electrical field stimulation | - |
dc.subject.keywordAuthor | graphene | - |