Ficolins do not alter host immune responses to lipopolysaccharide-induced inflammation in vivo

Abstract Ficolins are a family of pattern recognition molecules that are capable of activating the lectin pathway of complement. A limited number of reports have demonstrated a protective role of ficolins in animal models of infection. In addition, an immune modulatory role of ficolins has been sugg...

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Main Authors: Ninette Genster, Olga Østrup, Camilla Schjalm, Tom Eirik Mollnes, Jack B. Cowland, Peter Garred
Format: Article
Language:English
Published: Nature Publishing Group 2017-06-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-017-04121-w
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spelling doaj-9565494a7e254c2098c2868b24f37f7c2020-12-08T01:41:35ZengNature Publishing GroupScientific Reports2045-23222017-06-017111210.1038/s41598-017-04121-wFicolins do not alter host immune responses to lipopolysaccharide-induced inflammation in vivoNinette Genster0Olga Østrup1Camilla Schjalm2Tom Eirik Mollnes3Jack B. Cowland4Peter Garred5Laboratory of Molecular Medicine, Department of Clinical Immunology, Section 7631, Rigshospitalet, Faculty of Health and Medical Sciences, University of CopenhagenCenter for Genomic Medicine, Rigshospitalet, Copenhagen University HospitalDepartment of Immunology, Oslo University Hospital, RikshospitaletDepartment of Immunology, Oslo University Hospital, RikshospitaletThe Granulocyte Research Laboratory, Department of Hematology, Copenhagen University HospitalLaboratory of Molecular Medicine, Department of Clinical Immunology, Section 7631, Rigshospitalet, Faculty of Health and Medical Sciences, University of CopenhagenAbstract Ficolins are a family of pattern recognition molecules that are capable of activating the lectin pathway of complement. A limited number of reports have demonstrated a protective role of ficolins in animal models of infection. In addition, an immune modulatory role of ficolins has been suggested. Yet, the contribution of ficolins to inflammatory disease processes remains elusive. To address this, we investigated ficolin deficient mice during a lipopolysaccharide (LPS)-induced model of systemic inflammation. Although murine serum ficolin was shown to bind LPS in vitro, there was no difference between wildtype and ficolin deficient mice in morbidity and mortality by LPS-induced inflammation. Moreover, there was no difference between wildtype and ficolin deficient mice in the inflammatory cytokine profiles after LPS challenge. These findings were substantiated by microarray analysis revealing an unaltered spleen transcriptome profile in ficolin deficient mice compared to wildtype mice. Collectively, results from this study demonstrate that ficolins are not involved in host response to LPS-induced systemic inflammation.https://doi.org/10.1038/s41598-017-04121-w
collection DOAJ
language English
format Article
sources DOAJ
author Ninette Genster
Olga Østrup
Camilla Schjalm
Tom Eirik Mollnes
Jack B. Cowland
Peter Garred
spellingShingle Ninette Genster
Olga Østrup
Camilla Schjalm
Tom Eirik Mollnes
Jack B. Cowland
Peter Garred
Ficolins do not alter host immune responses to lipopolysaccharide-induced inflammation in vivo
Scientific Reports
author_facet Ninette Genster
Olga Østrup
Camilla Schjalm
Tom Eirik Mollnes
Jack B. Cowland
Peter Garred
author_sort Ninette Genster
title Ficolins do not alter host immune responses to lipopolysaccharide-induced inflammation in vivo
title_short Ficolins do not alter host immune responses to lipopolysaccharide-induced inflammation in vivo
title_full Ficolins do not alter host immune responses to lipopolysaccharide-induced inflammation in vivo
title_fullStr Ficolins do not alter host immune responses to lipopolysaccharide-induced inflammation in vivo
title_full_unstemmed Ficolins do not alter host immune responses to lipopolysaccharide-induced inflammation in vivo
title_sort ficolins do not alter host immune responses to lipopolysaccharide-induced inflammation in vivo
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2017-06-01
description Abstract Ficolins are a family of pattern recognition molecules that are capable of activating the lectin pathway of complement. A limited number of reports have demonstrated a protective role of ficolins in animal models of infection. In addition, an immune modulatory role of ficolins has been suggested. Yet, the contribution of ficolins to inflammatory disease processes remains elusive. To address this, we investigated ficolin deficient mice during a lipopolysaccharide (LPS)-induced model of systemic inflammation. Although murine serum ficolin was shown to bind LPS in vitro, there was no difference between wildtype and ficolin deficient mice in morbidity and mortality by LPS-induced inflammation. Moreover, there was no difference between wildtype and ficolin deficient mice in the inflammatory cytokine profiles after LPS challenge. These findings were substantiated by microarray analysis revealing an unaltered spleen transcriptome profile in ficolin deficient mice compared to wildtype mice. Collectively, results from this study demonstrate that ficolins are not involved in host response to LPS-induced systemic inflammation.
url https://doi.org/10.1038/s41598-017-04121-w
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