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Pentraxins CRP-I and CRP-II are post-translationally deiminated and differ in tissue specificity in cod (Gadus morhua L.) ontogeny

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dc.contributor Háskóli Íslands (HÍ)
dc.contributor University of Iceland (UI)
dc.contributor.author Magnadottir, Bergljot
dc.contributor.author Hayes, Polly
dc.contributor.author Gísladóttir, Berglind
dc.contributor.author Bragason, Birkir
dc.contributor.author Hristova, Mariya
dc.contributor.author Nicholas, Anthony P.
dc.contributor.author Guðmundsdóttir, Sigríður
dc.contributor.author Lange, Sigrun
dc.date.accessioned 2019-12-19T11:07:06Z
dc.date.available 2019-12-19T11:07:06Z
dc.date.issued 2018-10
dc.identifier.citation Magnadóttir, B., Hayes, P., Gísladóttir, B., Bragason, B. Þ., Hristova, M., Nicholas, A. P., . . . Lange, S. (2018). Pentraxins CRP-I and CRP-II are post-translationally deiminated and differ in tissue specificity in cod (Gadus morhua L.) ontogeny. Developmental & Comparative Immunology, 87, 1-11. doi:https://doi.org/10.1016/j.dci.2018.05.014
dc.identifier.issn 0145-305X
dc.identifier.uri https://hdl.handle.net/20.500.11815/1410
dc.description Publisher's version (útgefin grein)
dc.description.abstract Pentraxins arefluid phase pattern recognition molecules that form an important part of the innate immunedefence and are conserved betweenfish and human. In Atlantic cod (Gadus morhuaL.), two pentraxin-likeproteins have been described, CRP-I and CRP-II. Here we show for thefirst time that these two CRP forms arepost-translationally deiminated (an irreversible conversion of arginine to citrulline) and differ with respect totissue specific localisation in cod ontogeny from 3 to 84 days post hatching. While both forms are expressed inliver, albeit at temporally differing levels, CRP-I shows a strong association with nervous tissue while CRP-II isstrongly associated to mucosal tissues of gut and skin. This indicates differing roles for the two pentraxin types inimmune responses and tissue remodelling, also elucidating novel roles for CRP-I in the nervous system. Thepresence of deimination positive bands for cod CRPs varied somewhat between mucus and serum, possiblyfacilitating CRP protein moonlighting, allowing the same protein to exhibit a range of biological functions andthus meeting different functional requirements in different tissues. The presentedfindings may further currentunderstanding of the diverse roles of pentraxins in teleost immune defences and tissue remodelling, as well as invarious human pathologies, including autoimmune diseases, amyloidosis and cancer.
dc.description.sponsorship Thanks are due to Matthías Oddgeirsson, Agnar Steinarsson and other staff the staff at the Marine Institute's Mariculture Laboratory, Staður Grindavík, Iceland for providing sampling facilities and the fish. The authors also thank Margrét Jónsdóttir, Keldur, Institute for Experimental Pathology University of Iceland, for cod larvae sample preparation. This work was partly supported by The Icelandic Research Council (RANNIS), EC grant Fishaid QLK2-CT-2000-01076 and a University of Westminster start-up grant to SL. The authors declare no competing interest.
dc.format.extent 1-11
dc.language.iso en
dc.publisher Elsevier BV
dc.relation.ispartofseries Developmental and Comparative Immunology;87
dc.rights info:eu-repo/semantics/openAccess
dc.subject Immunology
dc.subject Developmental Biology
dc.subject Pentraxin (CRP, SAP)
dc.subject Protein deimination
dc.subject Mucosal immunity
dc.subject Amyloid
dc.subject Autoimmunity
dc.subject Cod (Gadus morhuaL.)
dc.subject Ontogeny
dc.subject Ónæmisfræði
dc.subject Þroskunarfræði
dc.subject Þorskur
dc.subject Prótín
dc.subject ÓNÆMI
dc.title Pentraxins CRP-I and CRP-II are post-translationally deiminated and differ in tissue specificity in cod (Gadus morhua L.) ontogeny
dc.type info:eu-repo/semantics/article
dcterms.license This is an open access article under the CC BY license (http://creativecommons.org/licenses/BY/4.0/).T
dc.description.version Peer Reviewed
dc.identifier.journal Developmental & Comparative Immunology
dc.identifier.doi 10.1016/j.dci.2018.05.014
dc.contributor.department Tilraunastöð í meinafræði að Keldum (HÍ)
dc.contributor.department Institute for Experimental Pathology, Keldur (UI)


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