Fabrication and operation of GRIN probes for in vivo fluorescence cellular imaging of internal organs in small animals

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dc.contributor.authorKim, Jun Kiko
dc.contributor.authorLee, Woei Mingko
dc.contributor.authorKim, Pilhanko
dc.contributor.authorChoi, Myunghwanko
dc.contributor.authorJung, Keehoonko
dc.contributor.authorKim, Seonghoonko
dc.contributor.authorYun, Seok Hyunko
dc.date.accessioned2013-03-12T23:01:32Z-
dc.date.available2013-03-12T23:01:32Z-
dc.date.created2012-08-17-
dc.date.created2012-08-17-
dc.date.created2012-08-17-
dc.date.issued2012-08-
dc.identifier.citationNATURE PROTOCOLS, v.7, no.8, pp.1456 - 1469-
dc.identifier.issn1754-2189-
dc.identifier.urihttp://hdl.handle.net/10203/103797-
dc.description.abstractIntravital fluorescence microscopy has emerged as a powerful technique to visualize cellular processes in vivo. However, owing to their size, the objective lenses required have limited physical accessibility to various tissue sites in the internal organs of small animals. The use of small-diameter probes using graded-index (GRIN) lenses expands the capabilities of conventional intravital microscopes to minimally invasive imaging of internal organs. In this protocol, we describe the detailed steps for the fabrication of front-and side-view GRIN probes and the integration and operation of the probes in a confocal microscope to enable visualization of fluorescent cells and microvasculature in various mouse organs. Some experience in building an optical setup is required to complete the protocol. We also present longitudinal imaging of immune cells in renal allografts and tumor development in the colon. Fabrication and integration can be completed in 5-7 h, and a typical in vivo imaging session takes 1-2 h.-
dc.languageEnglish-
dc.publisherNATURE PUBLISHING GROUP-
dc.subjectENDOSCOPY-
dc.subjectMICE-
dc.subjectENDOMICROSCOPY-
dc.subjectMICROENDOSCOPY-
dc.subjectRESOLUTION-
dc.subjectCANCER-
dc.subjectCELLS-
dc.titleFabrication and operation of GRIN probes for in vivo fluorescence cellular imaging of internal organs in small animals-
dc.typeArticle-
dc.identifier.wosid000306845200002-
dc.identifier.scopusid2-s2.0-84864427563-
dc.type.rimsART-
dc.citation.volume7-
dc.citation.issue8-
dc.citation.beginningpage1456-
dc.citation.endingpage1469-
dc.citation.publicationnameNATURE PROTOCOLS-
dc.identifier.doi10.1038/nprot.2012.078-
dc.contributor.localauthorKim, Pilhan-
dc.contributor.nonIdAuthorKim, Jun Ki-
dc.contributor.nonIdAuthorLee, Woei Ming-
dc.contributor.nonIdAuthorChoi, Myunghwan-
dc.contributor.nonIdAuthorJung, Keehoon-
dc.type.journalArticleArticle-
dc.subject.keywordPlusENDOSCOPY-
dc.subject.keywordPlusMICE-
dc.subject.keywordPlusENDOMICROSCOPY-
dc.subject.keywordPlusMICROENDOSCOPY-
dc.subject.keywordPlusRESOLUTION-
dc.subject.keywordPlusCANCER-
dc.subject.keywordPlusCELLS-
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