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Inflammatory responses in primary muscle cell cultures in Atlantic salmon (Salmo salar)

BACKGROUND: The relationship between fish health and muscle growth is critical for continued expansion of the aquaculture industry. The effect of immune stimulation on the expression of genes related to the energy balance of fish is poorly understood. In mammals immune stimulation results in major t...

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Autores principales: Pooley, Nicholas J, Tacchi, Luca, Secombes, Christopher J, Martin, Samuel AM
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3819742/
https://www.ncbi.nlm.nih.gov/pubmed/24180744
http://dx.doi.org/10.1186/1471-2164-14-747
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author Pooley, Nicholas J
Tacchi, Luca
Secombes, Christopher J
Martin, Samuel AM
author_facet Pooley, Nicholas J
Tacchi, Luca
Secombes, Christopher J
Martin, Samuel AM
author_sort Pooley, Nicholas J
collection PubMed
description BACKGROUND: The relationship between fish health and muscle growth is critical for continued expansion of the aquaculture industry. The effect of immune stimulation on the expression of genes related to the energy balance of fish is poorly understood. In mammals immune stimulation results in major transcriptional changes in muscle, potentially to allow a reallocation of amino acids for use in the immune response and energy homeostasis. The aim of this study was to investigate the effects of immune stimulation on fish muscle gene expression. RESULTS: Atlantic salmon (Salmo salar) primary muscle cell cultures were stimulated with recombinant (r)IL-1β, a major proinflammatory cytokine, for 24 h in order to simulate an acute immune response. The transcriptomic response was determined by RNA hybridization to a 4 × 44 K Agilent Atlantic salmon microarray platform. The rIL-1β stimulation induced the expression of genes related to both the innate and adaptive immune systems. In addition there were highly significant changes in the expression of genes related to regulation of the cell cycle, growth/structural proteins, proteolysis and lipid metabolism. Of interest were a number of IGF binding proteins that were differentially expressed, which may demonstrate cross talk between the growth and immune systems. CONCLUSION: We show rIL-1β modulates the expression of not only immune related genes, but also that of genes involved in processes related to growth and metabolism. Co-stimulation of muscle cells with both rIGF-I and rIL-1β demonstrates cross talk between these pathways providing potential avenues for further research. This study highlights the potential negative effects of inflammation on muscle protein deposition and growth in fish and extends our understanding of energy allocation in ectothermic animals.
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spelling pubmed-38197422013-11-08 Inflammatory responses in primary muscle cell cultures in Atlantic salmon (Salmo salar) Pooley, Nicholas J Tacchi, Luca Secombes, Christopher J Martin, Samuel AM BMC Genomics Research Article BACKGROUND: The relationship between fish health and muscle growth is critical for continued expansion of the aquaculture industry. The effect of immune stimulation on the expression of genes related to the energy balance of fish is poorly understood. In mammals immune stimulation results in major transcriptional changes in muscle, potentially to allow a reallocation of amino acids for use in the immune response and energy homeostasis. The aim of this study was to investigate the effects of immune stimulation on fish muscle gene expression. RESULTS: Atlantic salmon (Salmo salar) primary muscle cell cultures were stimulated with recombinant (r)IL-1β, a major proinflammatory cytokine, for 24 h in order to simulate an acute immune response. The transcriptomic response was determined by RNA hybridization to a 4 × 44 K Agilent Atlantic salmon microarray platform. The rIL-1β stimulation induced the expression of genes related to both the innate and adaptive immune systems. In addition there were highly significant changes in the expression of genes related to regulation of the cell cycle, growth/structural proteins, proteolysis and lipid metabolism. Of interest were a number of IGF binding proteins that were differentially expressed, which may demonstrate cross talk between the growth and immune systems. CONCLUSION: We show rIL-1β modulates the expression of not only immune related genes, but also that of genes involved in processes related to growth and metabolism. Co-stimulation of muscle cells with both rIGF-I and rIL-1β demonstrates cross talk between these pathways providing potential avenues for further research. This study highlights the potential negative effects of inflammation on muscle protein deposition and growth in fish and extends our understanding of energy allocation in ectothermic animals. BioMed Central 2013-11-01 /pmc/articles/PMC3819742/ /pubmed/24180744 http://dx.doi.org/10.1186/1471-2164-14-747 Text en Copyright © 2013 Pooley et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Pooley, Nicholas J
Tacchi, Luca
Secombes, Christopher J
Martin, Samuel AM
Inflammatory responses in primary muscle cell cultures in Atlantic salmon (Salmo salar)
title Inflammatory responses in primary muscle cell cultures in Atlantic salmon (Salmo salar)
title_full Inflammatory responses in primary muscle cell cultures in Atlantic salmon (Salmo salar)
title_fullStr Inflammatory responses in primary muscle cell cultures in Atlantic salmon (Salmo salar)
title_full_unstemmed Inflammatory responses in primary muscle cell cultures in Atlantic salmon (Salmo salar)
title_short Inflammatory responses in primary muscle cell cultures in Atlantic salmon (Salmo salar)
title_sort inflammatory responses in primary muscle cell cultures in atlantic salmon (salmo salar)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3819742/
https://www.ncbi.nlm.nih.gov/pubmed/24180744
http://dx.doi.org/10.1186/1471-2164-14-747
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