Intravital imaging of the kidney

dc.contributor.authorHato, Takashi
dc.contributor.authorWinfree, Seth
dc.contributor.authorDagher, Pierre C.
dc.contributor.departmentMedicine, School of Medicineen_US
dc.date.accessioned2018-03-06T19:35:26Z
dc.date.available2018-03-06T19:35:26Z
dc.date.issued2017-09-01
dc.description.abstractTwo-photon intravital microscopy is a powerful tool that allows the examination of dynamic cellular processes in the live animal with unprecedented resolution. Indeed, it offers the ability to address unique biological questions that may not be solved by other means. While two-photon intravital microscopy has been successfully applied to study many organs, the kidney presents its own unique challenges that need to be overcome in order to optimize and validate imaging data. For kidney imaging, the complexity of renal architecture and salient autofluorescence merit special considerations as these elements directly impact image acquisition and data interpretation. Here, using illustrative cases, we provide practical guides and discuss issues that may arise during two-photon live imaging of the rodent kidney.en_US
dc.eprint.versionAuthor's manuscripten_US
dc.identifier.citationHato, T., Winfree, S., & Dagher, P. C. (2017). Intravital imaging of the kidney. Methods (San Diego, Calif.), 128, 33–39. https://doi.org/10.1016/j.ymeth.2017.03.024en_US
dc.identifier.issn1046-2023en_US
dc.identifier.urihttps://hdl.handle.net/1805/15378
dc.language.isoen_USen_US
dc.publisherElsevieren_US
dc.relation.isversionof10.1016/j.ymeth.2017.03.024en_US
dc.relation.journalMethods (San Diego, Calif.)en_US
dc.rightsPublisher Policyen_US
dc.sourcePMCen_US
dc.subjectintravital microscopyen_US
dc.subjectkidneyen_US
dc.subjectrenal architectureen_US
dc.titleIntravital imaging of the kidneyen_US
dc.typeArticleen_US
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