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Innovation in Nucleotide-Binding Oligomerization-Like Receptor and Toll-Like Receptor Sensing Drives the Major Histocompatibility Complex-II Free Atlantic Cod Immune System

The absence of MHC class II antigen presentation and multiple pathogen recognition receptors in the Atlantic cod has not impaired its immune response however how underlying mechanisms have adapted remains largely unknown. In this study, ex vivo cod macrophages were challenged with various bacterial...

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Autores principales: Jin, Xingkun, Morro, Bernat, Tørresen, Ole K., Moiche, Visila, Solbakken, Monica H., Jakobsen, Kjetill S., Jentoft, Sissel, MacKenzie, Simon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7759675/
https://www.ncbi.nlm.nih.gov/pubmed/33362798
http://dx.doi.org/10.3389/fimmu.2020.609456
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author Jin, Xingkun
Morro, Bernat
Tørresen, Ole K.
Moiche, Visila
Solbakken, Monica H.
Jakobsen, Kjetill S.
Jentoft, Sissel
MacKenzie, Simon
author_facet Jin, Xingkun
Morro, Bernat
Tørresen, Ole K.
Moiche, Visila
Solbakken, Monica H.
Jakobsen, Kjetill S.
Jentoft, Sissel
MacKenzie, Simon
author_sort Jin, Xingkun
collection PubMed
description The absence of MHC class II antigen presentation and multiple pathogen recognition receptors in the Atlantic cod has not impaired its immune response however how underlying mechanisms have adapted remains largely unknown. In this study, ex vivo cod macrophages were challenged with various bacterial and viral microbe-associated molecular patterns (MAMP) to identify major response pathways. Cytosolic MAMP-PRR pathways based upon the NOD-like receptors (NLRs) and RIG-I-like receptors (RLRs) were identified as the critical response pathways. Our analyses suggest that internalization of exogenous ligands through scavenger receptors drives both pathways activating transcription factors like NF-kB (Nuclear factor-kappa B) and interferon regulatory factors (IRFs). Further, ligand-dependent differential expression of a unique TLR25 isoform and multiple NLR paralogues suggests (sub)neofunctionalization toward specific immune defensive strategies. Our results further demonstrate that the unique immune system of the Atlantic cod provides an unprecedented opportunity to explore the evolutionary history of PRR-based signaling in vertebrate immunity.
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spelling pubmed-77596752020-12-26 Innovation in Nucleotide-Binding Oligomerization-Like Receptor and Toll-Like Receptor Sensing Drives the Major Histocompatibility Complex-II Free Atlantic Cod Immune System Jin, Xingkun Morro, Bernat Tørresen, Ole K. Moiche, Visila Solbakken, Monica H. Jakobsen, Kjetill S. Jentoft, Sissel MacKenzie, Simon Front Immunol Immunology The absence of MHC class II antigen presentation and multiple pathogen recognition receptors in the Atlantic cod has not impaired its immune response however how underlying mechanisms have adapted remains largely unknown. In this study, ex vivo cod macrophages were challenged with various bacterial and viral microbe-associated molecular patterns (MAMP) to identify major response pathways. Cytosolic MAMP-PRR pathways based upon the NOD-like receptors (NLRs) and RIG-I-like receptors (RLRs) were identified as the critical response pathways. Our analyses suggest that internalization of exogenous ligands through scavenger receptors drives both pathways activating transcription factors like NF-kB (Nuclear factor-kappa B) and interferon regulatory factors (IRFs). Further, ligand-dependent differential expression of a unique TLR25 isoform and multiple NLR paralogues suggests (sub)neofunctionalization toward specific immune defensive strategies. Our results further demonstrate that the unique immune system of the Atlantic cod provides an unprecedented opportunity to explore the evolutionary history of PRR-based signaling in vertebrate immunity. Frontiers Media S.A. 2020-12-11 /pmc/articles/PMC7759675/ /pubmed/33362798 http://dx.doi.org/10.3389/fimmu.2020.609456 Text en Copyright © 2020 Jin, Morro, Tørresen, Moiche, Solbakken, Jakobsen, Jentoft and MacKenzie http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Jin, Xingkun
Morro, Bernat
Tørresen, Ole K.
Moiche, Visila
Solbakken, Monica H.
Jakobsen, Kjetill S.
Jentoft, Sissel
MacKenzie, Simon
Innovation in Nucleotide-Binding Oligomerization-Like Receptor and Toll-Like Receptor Sensing Drives the Major Histocompatibility Complex-II Free Atlantic Cod Immune System
title Innovation in Nucleotide-Binding Oligomerization-Like Receptor and Toll-Like Receptor Sensing Drives the Major Histocompatibility Complex-II Free Atlantic Cod Immune System
title_full Innovation in Nucleotide-Binding Oligomerization-Like Receptor and Toll-Like Receptor Sensing Drives the Major Histocompatibility Complex-II Free Atlantic Cod Immune System
title_fullStr Innovation in Nucleotide-Binding Oligomerization-Like Receptor and Toll-Like Receptor Sensing Drives the Major Histocompatibility Complex-II Free Atlantic Cod Immune System
title_full_unstemmed Innovation in Nucleotide-Binding Oligomerization-Like Receptor and Toll-Like Receptor Sensing Drives the Major Histocompatibility Complex-II Free Atlantic Cod Immune System
title_short Innovation in Nucleotide-Binding Oligomerization-Like Receptor and Toll-Like Receptor Sensing Drives the Major Histocompatibility Complex-II Free Atlantic Cod Immune System
title_sort innovation in nucleotide-binding oligomerization-like receptor and toll-like receptor sensing drives the major histocompatibility complex-ii free atlantic cod immune system
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7759675/
https://www.ncbi.nlm.nih.gov/pubmed/33362798
http://dx.doi.org/10.3389/fimmu.2020.609456
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