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Stress and innate immunity in carp: Corticosteroid receptors and pro-inflammatory cytokines

The stress hormone cortisol is deeply involved in immune regulation in all vertebrates. Common carp ( Cyprinus carpio L.) express four corticoid receptors that may modulate immune responses: three glucocorticoid receptors (GR); GR1, with two splice variants (GR1a and GR1b), GR2 and a single mineralo...

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Published in:Molecular immunology 2008-11, Vol.46 (1), p.70-79
Main Authors: Stolte, Ellen H., Nabuurs, Sander B., Bury, Nic R., Sturm, Armin, Flik, Gert, Savelkoul, Huub F.J., Lidy Verburg-van Kemenade, B.M.
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cited_by cdi_FETCH-LOGICAL-c554t-5122e7527e90308cf303347d100af76792d901865b9b8373089edd5aab174afe3
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container_title Molecular immunology
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creator Stolte, Ellen H.
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description The stress hormone cortisol is deeply involved in immune regulation in all vertebrates. Common carp ( Cyprinus carpio L.) express four corticoid receptors that may modulate immune responses: three glucocorticoid receptors (GR); GR1, with two splice variants (GR1a and GR1b), GR2 and a single mineralocorticoid receptor (MR). All receptors are expressed as of 4 days post-fertilization and may thus play a critical role in development and functioning of the adult immune system. Immune tissues and cells predominantly express mRNA for GRs compared to mRNA for the MR. Three-dimensional protein structure modeling predicts, and transfection assays confirm that alternative splicing of GR1 does not influence the capacity to induce transcription of effector genes. When tested for cortisol activation, GR2 is the most sensitive corticoid receptor in carp, followed by the MR and GR1a and GR1b. Lipopolysacharide (LPS) treatment of head kidney phagocytes quickly induces GR1 expression and inhibits GR2 expression. Cortisol treatment in vivo enhances GR1a and MR mRNA expression, but only mildly, and cortisol treatment in vitro does not affect receptor expression of phagocytes. Cortisol has no direct effect on the LPS-induced receptor profile. Therefore, an immune rather than a stress stimulus regulates GR expression. Cortisol administered at stress levels to phagocytes in vitro significantly inhibits LPS-induced expression of the pro-inflammatory cytokines tumor necrosis factor alpha (TNF-α) and interleukin-12 (IL-12) (subunit p35) and of inducible nitric oxide synthase ( iNOS) expression. A physiologically differential function for GR1 and GR2 in the immune response of fish to infection is indicated.
doi_str_mv 10.1016/j.molimm.2008.07.022
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Common carp ( Cyprinus carpio L.) express four corticoid receptors that may modulate immune responses: three glucocorticoid receptors (GR); GR1, with two splice variants (GR1a and GR1b), GR2 and a single mineralocorticoid receptor (MR). All receptors are expressed as of 4 days post-fertilization and may thus play a critical role in development and functioning of the adult immune system. Immune tissues and cells predominantly express mRNA for GRs compared to mRNA for the MR. Three-dimensional protein structure modeling predicts, and transfection assays confirm that alternative splicing of GR1 does not influence the capacity to induce transcription of effector genes. When tested for cortisol activation, GR2 is the most sensitive corticoid receptor in carp, followed by the MR and GR1a and GR1b. Lipopolysacharide (LPS) treatment of head kidney phagocytes quickly induces GR1 expression and inhibits GR2 expression. Cortisol treatment in vivo enhances GR1a and MR mRNA expression, but only mildly, and cortisol treatment in vitro does not affect receptor expression of phagocytes. Cortisol has no direct effect on the LPS-induced receptor profile. Therefore, an immune rather than a stress stimulus regulates GR expression. Cortisol administered at stress levels to phagocytes in vitro significantly inhibits LPS-induced expression of the pro-inflammatory cytokines tumor necrosis factor alpha (TNF-α) and interleukin-12 (IL-12) (subunit p35) and of inducible nitric oxide synthase ( iNOS) expression. 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Common carp ( Cyprinus carpio L.) express four corticoid receptors that may modulate immune responses: three glucocorticoid receptors (GR); GR1, with two splice variants (GR1a and GR1b), GR2 and a single mineralocorticoid receptor (MR). All receptors are expressed as of 4 days post-fertilization and may thus play a critical role in development and functioning of the adult immune system. Immune tissues and cells predominantly express mRNA for GRs compared to mRNA for the MR. Three-dimensional protein structure modeling predicts, and transfection assays confirm that alternative splicing of GR1 does not influence the capacity to induce transcription of effector genes. When tested for cortisol activation, GR2 is the most sensitive corticoid receptor in carp, followed by the MR and GR1a and GR1b. Lipopolysacharide (LPS) treatment of head kidney phagocytes quickly induces GR1 expression and inhibits GR2 expression. Cortisol treatment in vivo enhances GR1a and MR mRNA expression, but only mildly, and cortisol treatment in vitro does not affect receptor expression of phagocytes. Cortisol has no direct effect on the LPS-induced receptor profile. Therefore, an immune rather than a stress stimulus regulates GR expression. Cortisol administered at stress levels to phagocytes in vitro significantly inhibits LPS-induced expression of the pro-inflammatory cytokines tumor necrosis factor alpha (TNF-α) and interleukin-12 (IL-12) (subunit p35) and of inducible nitric oxide synthase ( iNOS) expression. A physiologically differential function for GR1 and GR2 in the immune response of fish to infection is indicated.</description><subject>Alternative splicing</subject><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Carps - genetics</subject><subject>Carps - immunology</subject><subject>Common carp</subject><subject>Cyprinus carpio</subject><subject>Cytokine expression</subject><subject>Cytokines - genetics</subject><subject>Cytokines - metabolism</subject><subject>differential expression</subject><subject>DNA - metabolism</subject><subject>dna-binding domain</subject><subject>early-life stages</subject><subject>fish glucocorticoid-receptor</subject><subject>functional-characterization</subject><subject>Hydrocortisone - pharmacology</subject><subject>Immune system</subject><subject>Immunity, Innate - drug effects</subject><subject>Immunity, Innate - immunology</subject><subject>Inflammation Mediators - metabolism</subject><subject>Kidney - cytology</subject><subject>Kidney - drug effects</subject><subject>Kidney - enzymology</subject><subject>Lipopolysaccharides - pharmacology</subject><subject>mineralocorticoid receptor</subject><subject>Molecular Sequence Data</subject><subject>Nitric Oxide Synthase Type II - genetics</subject><subject>Nitric Oxide Synthase Type II - metabolism</subject><subject>Phagocytes - drug effects</subject><subject>Phagocytes - enzymology</subject><subject>Protein Binding - drug effects</subject><subject>Protein Structure, Tertiary</subject><subject>Receptors, Steroid - chemistry</subject><subject>Receptors, Steroid - genetics</subject><subject>Receptors, Steroid - metabolism</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Species Specificity</subject><subject>Stress, Physiological - drug effects</subject><subject>Stress, Physiological - immunology</subject><subject>Structural Homology, Protein</subject><subject>Teleost</subject><subject>teleost fish</subject><subject>Transcriptional Activation - drug effects</subject><subject>trypanoplasma-borreli</subject><issn>0161-5890</issn><issn>1872-9142</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqFkcFu1DAQhi0EokvpGyCUE7eEsZPYTg9IaNXSSpU4ACcOluNMkJfEDrbTat--XmUlbnDxyNb3j8f-CHlHoaJA-cdDNfvJznPFAGQFogLGXpAdlYKVHW3YS7LLGC1b2cEFeRPjAQA48PY1uaBSQiM535Gf31LAGAvthsI6pxMWuefqbDrmfWF0WK6LvQ_JGh8TBm-HIqDBJfmwpZbgS-vGSc-zzofHwhyT_20dxrfk1ainiFfnekl-3N5839-VD1-_3O8_P5SmbZtUtpQxFC0T2EEN0ow11HUjBgqgR8FFx4YOqORt3_WyFhnpcBharXsqGj1ifUmut75P-hc66_KinA7GRuW1VZPtgw5H9bQG5aZTWdY-qlowaFgOf9jC-R1_VoxJzTYanCbt0K9R8Y4Lnuf5L8igEw3UNIPNBprgYww4qiXY-TQBBXVSpw5qU6dO6hQIldXl2Ptz_7WfcfgbOrvKwKcNwPyXjxaDisaiMzjYbCSpwdt_3_AMQiauXA</recordid><startdate>20081101</startdate><enddate>20081101</enddate><creator>Stolte, Ellen H.</creator><creator>Nabuurs, Sander B.</creator><creator>Bury, Nic R.</creator><creator>Sturm, Armin</creator><creator>Flik, Gert</creator><creator>Savelkoul, Huub F.J.</creator><creator>Lidy Verburg-van Kemenade, B.M.</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope><scope>QVL</scope></search><sort><creationdate>20081101</creationdate><title>Stress and innate immunity in carp: Corticosteroid receptors and pro-inflammatory cytokines</title><author>Stolte, Ellen H. ; 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Cortisol treatment in vivo enhances GR1a and MR mRNA expression, but only mildly, and cortisol treatment in vitro does not affect receptor expression of phagocytes. Cortisol has no direct effect on the LPS-induced receptor profile. Therefore, an immune rather than a stress stimulus regulates GR expression. Cortisol administered at stress levels to phagocytes in vitro significantly inhibits LPS-induced expression of the pro-inflammatory cytokines tumor necrosis factor alpha (TNF-α) and interleukin-12 (IL-12) (subunit p35) and of inducible nitric oxide synthase ( iNOS) expression. A physiologically differential function for GR1 and GR2 in the immune response of fish to infection is indicated.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>18804866</pmid><doi>10.1016/j.molimm.2008.07.022</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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subjects Alternative splicing
Amino Acid Sequence
Animals
Carps - genetics
Carps - immunology
Common carp
Cyprinus carpio
Cytokine expression
Cytokines - genetics
Cytokines - metabolism
differential expression
DNA - metabolism
dna-binding domain
early-life stages
fish glucocorticoid-receptor
functional-characterization
Hydrocortisone - pharmacology
Immune system
Immunity, Innate - drug effects
Immunity, Innate - immunology
Inflammation Mediators - metabolism
Kidney - cytology
Kidney - drug effects
Kidney - enzymology
Lipopolysaccharides - pharmacology
mineralocorticoid receptor
Molecular Sequence Data
Nitric Oxide Synthase Type II - genetics
Nitric Oxide Synthase Type II - metabolism
Phagocytes - drug effects
Phagocytes - enzymology
Protein Binding - drug effects
Protein Structure, Tertiary
Receptors, Steroid - chemistry
Receptors, Steroid - genetics
Receptors, Steroid - metabolism
RNA, Messenger - genetics
RNA, Messenger - metabolism
Species Specificity
Stress, Physiological - drug effects
Stress, Physiological - immunology
Structural Homology, Protein
Teleost
teleost fish
Transcriptional Activation - drug effects
trypanoplasma-borreli
title Stress and innate immunity in carp: Corticosteroid receptors and pro-inflammatory cytokines
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