Vis enkel innførsel

dc.contributor.authorPark, Youngjin
dc.contributor.authorAbihssira-García, Isabel S.
dc.contributor.authorThalmann, Sebastian
dc.contributor.authorWiegertjes, Geert
dc.contributor.authorBarreda, Daniel
dc.contributor.authorOlsvik, Pål Asgeir
dc.contributor.authorKiron, Viswanath
dc.date.accessioned2020-07-10T08:04:15Z
dc.date.available2020-07-10T08:04:15Z
dc.date.created2020-02-20T09:24:04Z
dc.date.issued2020
dc.identifier.citationPark, Y., Abihssira-Garcia, I. S., Thalmann, S., Wiegertjes, G. F., Barreda, D. R., Olsvik, P. A. & Kiron, V. (2020). Imaging flow cytometry protocols for examining phagocytosis of microplastics and bioparticles by immune cells of aquatic animals. Frontiers in Immunology, 11: 203. doi:en_US
dc.identifier.issn1664-3224
dc.identifier.urihttps://hdl.handle.net/11250/2663656
dc.description.abstractImaging flow cytometry (IFC) is a powerful tool which combines flow cytometry with digital microscopy to generate quantitative high-throughput imaging data. Despite various advantages of IFC over standard flow cytometry, widespread adoption of this technology for studies in aquatic sciences is limited, probably due to the relatively high equipment cost, complexity of image analysis-based data interpretation and lack of core facilities with trained personnel. Here, we describe the application of IFC to examine phagocytosis of particles including microplastics by cells from aquatic animals. For this purpose, we studied (1) live/dead cell assays and identification of cell types, (2) phagocytosis of degradable and non-degradable particles by Atlantic salmon head kidney cells and (3) the effect of incubation temperature on phagocytosis of degradable particles in three aquatic animals–Atlantic salmon, Nile tilapia, and blue mussel. The usefulness of the developed method was assessed by evaluating the effect of incubation temperature on phagocytosis. Our studies demonstrate that IFC provides significant benefits over standard flow cytometry in phagocytosis measurement by allowing integration of morphometric parameters, especially while identifying cell populations and distinguishing between different types of fluorescent particles and detecting their localization.en_US
dc.language.isoengen_US
dc.publisherFrontiersen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleImaging flow cytometry protocols for examining phagocytosis of microplastics and bioparticles by immune cells of aquatic animalsen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© 2020 The Author(s)en_US
dc.subject.nsiVDP::Matematikk og Naturvitenskap: 400::Basale biofag: 470::Cellebiologi: 471en_US
dc.source.pagenumber11en_US
dc.source.volume11en_US
dc.source.journalFrontiers in Immunologyen_US
dc.identifier.doi10.3389/fimmu.2020.00203
dc.identifier.cristin1795976
dc.relation.projectRegional Research Fund of Northern Norway: 272004en_US


Tilhørende fil(er)

Thumbnail

Denne innførselen finnes i følgende samling(er)

Vis enkel innførsel

Navngivelse 4.0 Internasjonal
Med mindre annet er angitt, så er denne innførselen lisensiert som Navngivelse 4.0 Internasjonal