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Cited 11 time in webofscience Cited 11 time in scopus
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dc.contributor.authorBok, S-
dc.contributor.authorWang, T-
dc.contributor.authorLee, CJ-
dc.contributor.authorJeon, SU-
dc.contributor.authorKim, YE-
dc.contributor.authorKim, J-
dc.contributor.authorHong, BJ-
dc.contributor.authorYoon, CJ-
dc.contributor.authorKim, S-
dc.contributor.authorLee, SH-
dc.contributor.authorKim, HJ-
dc.contributor.authorKim, IH-
dc.contributor.authorKIM, KI HEAN-
dc.contributor.authorAhn, GO-
dc.date.accessioned2017-07-19T11:39:37Z-
dc.date.available2017-07-19T11:39:37Z-
dc.date.created2015-10-20-
dc.date.issued2015-09-01-
dc.identifier.issn2156-7085-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/35274-
dc.description.abstractMicroglia are brain resident macrophages rapidly responding to various stimuli to exert appropriate inflammatory responses. Although they have recently been exploited as an attractive candidate for imaging neuroinflammation, it is still difficult to visualize them at the cellular and molecular levels. Here we imaged activated microglia by establishing intracranial window chamber (ICW) in a mouse model of focal cerebral ischemia by using two-photon microscopy (TPM), in vivo. Intravenous injection of fluorescent antibodies allowed us to detect significantly elevated levels of Iba-1 and CD68 positive activated microglia in the ipsilateral compared to the contralateral side of the infarct. We further observed that indomethacin, a non-steroidal anti-inflammatory drug significantly attenuated CD68-positive microglial activation in ICW, which was further confirmed by qRT-PCR biochemical analyses. In conclusion, we believe that in vivo TPM imaging of ICW would be a useful tool to screen for therapeutic interventions lowering microglial activation hence neuroinflammation. (C) 2015 Optical Society of America-
dc.languageEnglish-
dc.publisherOptical Society of America-
dc.relation.isPartOfBIOMEDICAL OPTICS EXPRESS-
dc.titleIn vivo imaging of activated microglia in a mouse model of focal cerebral ischemia by two-photon microscopy-
dc.typeArticle-
dc.identifier.doi10.1364/BOE.6.003303-
dc.type.rimsART-
dc.identifier.bibliographicCitationBIOMEDICAL OPTICS EXPRESS, v.6, no.9, pp.3303 - 3312-
dc.identifier.wosid000360888400017-
dc.date.tcdate2019-03-01-
dc.citation.endPage3312-
dc.citation.number9-
dc.citation.startPage3303-
dc.citation.titleBIOMEDICAL OPTICS EXPRESS-
dc.citation.volume6-
dc.contributor.affiliatedAuthorBok, S-
dc.contributor.affiliatedAuthorKim, YE-
dc.contributor.affiliatedAuthorKim, J-
dc.contributor.affiliatedAuthorHong, BJ-
dc.contributor.affiliatedAuthorKim, S-
dc.contributor.affiliatedAuthorKIM, KI HEAN-
dc.contributor.affiliatedAuthorAhn, GO-
dc.identifier.scopusid2-s2.0-84948735868-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc7-
dc.description.scptc3*
dc.date.scptcdate2018-05-121*
dc.type.docTypeArticle-
dc.subject.keywordPlusMULTIPHOTON MICROSCOPY-
dc.subject.keywordPlusSTROKE-
dc.subject.keywordPlusBRAIN-
dc.subject.keywordPlusFLUORESCENCE-
dc.subject.keywordPlusNEUROINFLAMMATION-
dc.subject.keywordPlusNEUROGENESIS-
dc.subject.keywordPlusMECHANISMS-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusLASER-
dc.subject.keywordPlusMICE-
dc.relation.journalWebOfScienceCategoryBiochemical Research Methods-
dc.relation.journalWebOfScienceCategoryOptics-
dc.relation.journalWebOfScienceCategoryRadiology, Nuclear Medicine & Medical Imaging-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaOptics-
dc.relation.journalResearchAreaRadiology, Nuclear Medicine & Medical Imaging-

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