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dc.contributor.author
Vladymyrov, Mykhailo
dc.contributor.author
Jahromi, Neda H.
dc.contributor.author
Kaba, Elisa
dc.contributor.author
Engelhardt, Britta
dc.contributor.author
Ariga, Akitaka
dc.date.accessioned
2020-02-12T08:16:12Z
dc.date.available
2020-02-12T02:57:29Z
dc.date.available
2020-02-12T08:16:12Z
dc.date.issued
2020-01
dc.identifier.issn
2296-424X
dc.identifier.other
10.3389/fphy.2019.00222
en_US
dc.identifier.uri
http://hdl.handle.net/20.500.11850/398597
dc.identifier.doi
10.3929/ethz-b-000398597
dc.description.abstract
Intravital multiphoton microscopy has become one of the central tools used in the investigation of dynamic cellular activity and function in living animals under nearly physiological conditions and is particularly important for studying the dynamic immune system. During intravital imaging in mice, periodic motion of tissue caused by respiration, induces significant shifts of the imaged region. In slow laser scanning imaging modalities, such as multiphoton microscopy, this movement can lead to considerable distortion and discontinuity in three dimensions of the acquired images. Here, we introduce VivoFollow 2, a toolkit that concurrent with image acquisition performs a precise measurement of the respective image distortion, enabling subsequent automated correction of the imaging data. Recovery of one three-dimensional image stack, corresponding to the tomographic tissue sectioning by the optical plane from each single raw image stack, preserves the time continuity within each image stack. Implementation of VivoFollow 2 thus enables a minimization of motion artifacts in tissues exposed to periodic movements and allows for long-term time-lapse imaging and subsequent precise image analysis of the dynamics of cellular and humoral factors in vivo.
en_US
dc.format
application/pdf
en_US
dc.language.iso
en
en_US
dc.publisher
Frontiers Media
dc.rights.uri
http://creativecommons.org/licenses/by/4.0/
dc.subject
intravital microscopy
en_US
dc.subject
multiphoton microscopy
en_US
dc.subject
tissue motion
en_US
dc.subject
GPU-accelerated data processing
en_US
dc.subject
real-time image processing
en_US
dc.subject
immune cell trafficking
en_US
dc.subject
cell migration
en_US
dc.title
VivoFollow 2: Distortion-Free Multiphoton Intravital Imaging
en_US
dc.type
Journal Article
dc.rights.license
Creative Commons Attribution 4.0 International
dc.date.published
2020-01-17
ethz.journal.title
Frontiers in Physics
ethz.journal.volume
7
en_US
ethz.pages.start
222
en_US
ethz.size
12 p.
en_US
ethz.version.deposit
publishedVersion
en_US
ethz.identifier.wos
ethz.identifier.scopus
ethz.publication.place
Lausanne
ethz.publication.status
published
en_US
ethz.date.deposited
2020-02-12T02:57:34Z
ethz.source
WOS
ethz.eth
yes
en_US
ethz.availability
Open access
en_US
ethz.rosetta.installDate
2020-02-12T08:16:22Z
ethz.rosetta.lastUpdated
2024-02-02T10:22:31Z
ethz.rosetta.versionExported
true
ethz.COinS
ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.atitle=VivoFollow%202:%20Distortion-Free%20Multiphoton%20Intravital%20Imaging&rft.jtitle=Frontiers%20in%20Physics&rft.date=2020-01&rft.volume=7&rft.spage=222&rft.issn=2296-424X&rft.au=Vladymyrov,%20Mykhailo&Jahromi,%20Neda%20H.&Kaba,%20Elisa&Engelhardt,%20Britta&Ariga,%20Akitaka&rft.genre=article&rft_id=info:doi/10.3389/fphy.2019.00222&
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