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dc.contributor.authorSmith, Nicole
dc.contributor.authorUmasuthan, Navaneethaiyer
dc.contributor.authorKumar, Surendra
dc.contributor.authorWoldemariam, Nardos Tesfaye
dc.contributor.authorAndreassen, Rune
dc.contributor.authorChristian, Sherri
dc.contributor.authorRise, Matthew L.
dc.date.accessioned2021-10-07T10:25:29Z
dc.date.available2021-10-07T10:25:29Z
dc.date.created2021-09-06T16:44:08Z
dc.date.issued2021-08-16
dc.identifier.issn1664-3224
dc.identifier.urihttps://hdl.handle.net/11250/2788354
dc.description.abstractThe Atlantic salmon (Salmo salar) is an economically important fish, both in aquaculture and in the wild. In vertebrates, macrophages are some of the first cell types to respond to pathogen infection and disease. While macrophage biology has been characterized in mammals, less is known in fish. Our previous work identified changes in the morphology, phagocytic ability, and miRNA profile of Atlantic salmon adherent head kidney leukocytes (HKLs) from predominantly “monocyte-like” at Day 1 of in vitro culture to predominantly “macrophage-like” at Day 5 of culture. Therefore, to further characterize these two cell populations, we examined the mRNA transcriptome profile in Day 1 and Day 5 HKLs using a 44K oligonucleotide microarray. Large changes in the transcriptome were revealed, including changes in the expression of macrophage and immune-related transcripts (e.g. csf1r, arg1, tnfa, mx2), lipid-related transcripts (e.g. fasn, dhcr7, fabp6), and transcription factors involved in macrophage differentiation and function (e.g. klf2, klf9, irf7, irf8, stat1). The in silico target prediction analysis of differentially expressed genes (DEGs) using miRNAs known to change expression in Day 5 HKLs, followed by gene pathway enrichment analysis, supported that these miRNAs may be involved in macrophage maturation by targeting specific DEGs. Elucidating how immune cells, such as macrophages, develop and function is a key step in understanding the Atlantic salmon immune system. Overall, the results indicate that, without the addition of exogenous factors, the adherent HKL cell population differentiates in vitro to become macrophage-like.en_US
dc.description.sponsorshipThis study was funded by Natural Sciences and Engineering Research Council of Canada (NSERC) Discovery Grants to MR (341304-2012 and 2020-04519), a Memorial University of Newfoundland Seed grant to SC (212779), a NSERC Discovery Grant to SC (2017-04630), a Norwegian Research Council grant to RA (280839/E40), and Genomic Applications Partnership Program projects [GAPP # 6604: Biomarker Platform for Commercial Aquaculture Feed Development project; and GAPP #6607: Integrated Pathogen Management of Co-infection in Atlantic salmon (IPMC) project] funded by the Government of Canada through Genome Canada and Genome Atlantic, and Cargill Innovation (formerly EWOS Innovation) to MR. The IPMC project was also funded by the Government of Newfoundland and Labrador through the Department of Tourism, Culture, Industry and Innovation (Leverage R&D award #5401-1019-108. NS was supported by a NSERC PGS D fellowship.en_US
dc.language.isoengen_US
dc.publisherFrontiers Mediaen_US
dc.relation.ispartofseriesFrontiers in Immunology;August 2021 | Volume 12 | Article 709910
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.subjectAtlantic salmonen_US
dc.subjectTranscriptomesen_US
dc.subjectMacrophagesen_US
dc.subjectMicroarraysen_US
dc.subjectCell differentiationsen_US
dc.subjectHead kidney leukocyte culturesen_US
dc.titleTranscriptome Profiling of Atlantic Salmon Adherent Head Kidney Leukocytes Reveals That Macrophages Are Selectively Enriched During Cultureen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright © 2021 Smith, Umasuthan, Kumar, Woldemariam, Andreassen, Christian and Rise.en_US
dc.source.articlenumber709910en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doihttps://doi.org/10.3389/fimmu.2021.709910
dc.identifier.cristin1931751
dc.source.journalFrontiers in Immunologyen_US
dc.source.volume12en_US
dc.source.pagenumber1-19en_US
dc.relation.projectNorges forskningsråd: 280839en_US


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