Serveur d'exploration sur la glutarédoxine

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Glutaredoxin 2 from big belly seahorse (Hippocampus abdominalis) and its potential involvement in cellular redox homeostasis and host immune responses.

Identifieur interne : 000164 ( Main/Exploration ); précédent : 000163; suivant : 000165

Glutaredoxin 2 from big belly seahorse (Hippocampus abdominalis) and its potential involvement in cellular redox homeostasis and host immune responses.

Auteurs : W K M. Omeka [Corée du Sud] ; D S Liyanage [Corée du Sud] ; Hyerim Yang [Corée du Sud] ; Jehee Lee [Corée du Sud]

Source :

RBID : pubmed:31586678

Descripteurs français

English descriptors

Abstract

Glutaredoxins are oxidoreductases present in almost all living organisms. They belong to the thioredoxin superfamily and share the thioredoxin structure and catalytic motif. Glutaredoxin 2 has been identified as a mitochondrial protein in vertebrates. In this study, the sequence of Glutaredoxin 2 from Hippocampus abdominalis (HaGrx2) was analyzed by molecular, transcriptional, and functional assays. In-silico analysis revealed that HaGrx2 shows the highest homology with Hippocampus comes, while distinctly cluster with fish Grx2 orthologs. Tissue distribution analysis showed that HaGrx2 is ubiquitously expressed in all tissues tested, and the highest expression was observed in the brain and skin. Significant HaGrx2 transcript modulation was identified in blood and liver upon injecting bacterial and Pathogen Associated Molecular Patterns. The redox activity of HaGrx2 was revealed by Dehydroascorbic reduction and insulin disulfide reduction activity assays. Further, the deglutathionylation activity of 1 nM HaGrx2 was found to be equivalent to that of 0.84 nM HaGrx1. HaGrx2 exhibited antiapoptotic activity against H2O2-induced oxidative stress in FHM cells. Altogether, the results of this study suggest that HaGrx2 plays a role in redox homeostasis and innate immune responses in fish.

DOI: 10.1016/j.fsi.2019.09.071
PubMed: 31586678


Affiliations:


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Le document en format XML

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<term>Base Sequence (MeSH)</term>
<term>Edwardsiella tarda (physiology)</term>
<term>Enterobacteriaceae Infections (immunology)</term>
<term>Enterobacteriaceae Infections (veterinary)</term>
<term>Female (MeSH)</term>
<term>Fish Diseases (immunology)</term>
<term>Fish Proteins (chemistry)</term>
<term>Fish Proteins (genetics)</term>
<term>Fish Proteins (immunology)</term>
<term>Gene Expression Profiling (veterinary)</term>
<term>Gene Expression Regulation (immunology)</term>
<term>Glutaredoxins (chemistry)</term>
<term>Glutaredoxins (genetics)</term>
<term>Glutaredoxins (immunology)</term>
<term>Homeostasis (MeSH)</term>
<term>Immunity, Innate (genetics)</term>
<term>Lipopolysaccharides (adverse effects)</term>
<term>Male (MeSH)</term>
<term>Oxidation-Reduction (MeSH)</term>
<term>Phylogeny (MeSH)</term>
<term>Poly I-C (adverse effects)</term>
<term>Sequence Alignment (veterinary)</term>
<term>Smegmamorpha (genetics)</term>
<term>Smegmamorpha (immunology)</term>
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<term>Analyse de profil d'expression de gènes (médecine vétérinaire)</term>
<term>Animaux (MeSH)</term>
<term>Edwardsiella tarda (physiologie)</term>
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<term>Glutarédoxines (composition chimique)</term>
<term>Glutarédoxines (génétique)</term>
<term>Glutarédoxines (immunologie)</term>
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<term>Immunité innée (génétique)</term>
<term>Infections à Enterobacteriaceae (immunologie)</term>
<term>Infections à Enterobacteriaceae (médecine vétérinaire)</term>
<term>Infections à streptocoques (immunologie)</term>
<term>Infections à streptocoques (médecine vétérinaire)</term>
<term>Lipopolysaccharides (effets indésirables)</term>
<term>Maladies des poissons (immunologie)</term>
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<term>Oxydoréduction (MeSH)</term>
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<term>Protéines de poisson (génétique)</term>
<term>Protéines de poisson (immunologie)</term>
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<term>Smegmamorpha (immunologie)</term>
<term>Streptococcus iniae (physiologie)</term>
<term>Séquence d'acides aminés (MeSH)</term>
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<term>Infections à Enterobacteriaceae</term>
<term>Infections à streptocoques</term>
<term>Maladies des poissons</term>
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<term>Fish Diseases</term>
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<term>Gene Expression Regulation</term>
<term>Glutaredoxins</term>
<term>Smegmamorpha</term>
<term>Streptococcal Infections</term>
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<term>Analyse de profil d'expression de gènes</term>
<term>Infections à Enterobacteriaceae</term>
<term>Infections à streptocoques</term>
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<term>Streptococcus iniae</term>
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<term>Edwardsiella tarda</term>
<term>Streptococcus iniae</term>
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<term>Enterobacteriaceae Infections</term>
<term>Gene Expression Profiling</term>
<term>Sequence Alignment</term>
<term>Streptococcal Infections</term>
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<term>Base Sequence</term>
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<term>Homeostasis</term>
<term>Male</term>
<term>Oxidation-Reduction</term>
<term>Phylogeny</term>
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<term>Animaux</term>
<term>Femelle</term>
<term>Homéostasie</term>
<term>Mâle</term>
<term>Oxydoréduction</term>
<term>Phylogenèse</term>
<term>Séquence d'acides aminés</term>
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<div type="abstract" xml:lang="en">Glutaredoxins are oxidoreductases present in almost all living organisms. They belong to the thioredoxin superfamily and share the thioredoxin structure and catalytic motif. Glutaredoxin 2 has been identified as a mitochondrial protein in vertebrates. In this study, the sequence of Glutaredoxin 2 from Hippocampus abdominalis (HaGrx2) was analyzed by molecular, transcriptional, and functional assays. In-silico analysis revealed that HaGrx2 shows the highest homology with Hippocampus comes, while distinctly cluster with fish Grx2 orthologs. Tissue distribution analysis showed that HaGrx2 is ubiquitously expressed in all tissues tested, and the highest expression was observed in the brain and skin. Significant HaGrx2 transcript modulation was identified in blood and liver upon injecting bacterial and Pathogen Associated Molecular Patterns. The redox activity of HaGrx2 was revealed by Dehydroascorbic reduction and insulin disulfide reduction activity assays. Further, the deglutathionylation activity of 1 nM HaGrx2 was found to be equivalent to that of 0.84 nM HaGrx1. HaGrx2 exhibited antiapoptotic activity against H
<sub>2</sub>
O
<sub>2</sub>
-induced oxidative stress in FHM cells. Altogether, the results of this study suggest that HaGrx2 plays a role in redox homeostasis and innate immune responses in fish.</div>
</front>
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<AbstractText>Glutaredoxins are oxidoreductases present in almost all living organisms. They belong to the thioredoxin superfamily and share the thioredoxin structure and catalytic motif. Glutaredoxin 2 has been identified as a mitochondrial protein in vertebrates. In this study, the sequence of Glutaredoxin 2 from Hippocampus abdominalis (HaGrx2) was analyzed by molecular, transcriptional, and functional assays. In-silico analysis revealed that HaGrx2 shows the highest homology with Hippocampus comes, while distinctly cluster with fish Grx2 orthologs. Tissue distribution analysis showed that HaGrx2 is ubiquitously expressed in all tissues tested, and the highest expression was observed in the brain and skin. Significant HaGrx2 transcript modulation was identified in blood and liver upon injecting bacterial and Pathogen Associated Molecular Patterns. The redox activity of HaGrx2 was revealed by Dehydroascorbic reduction and insulin disulfide reduction activity assays. Further, the deglutathionylation activity of 1 nM HaGrx2 was found to be equivalent to that of 0.84 nM HaGrx1. HaGrx2 exhibited antiapoptotic activity against H
<sub>2</sub>
O
<sub>2</sub>
-induced oxidative stress in FHM cells. Altogether, the results of this study suggest that HaGrx2 plays a role in redox homeostasis and innate immune responses in fish.</AbstractText>
<CopyrightInformation>Copyright © 2019 Elsevier Ltd. All rights reserved.</CopyrightInformation>
</Abstract>
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<Affiliation>Department of Marine Life Sciences & Fish Vaccine Research Center, Jeju National University, Jeju Self-Governing Province, 63243, Republic of Korea; Marine Science Institute, Jeju National University, Jeju Self-Governing Province, 63333, Republic of Korea.</Affiliation>
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<QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName>
<QualifierName UI="Q000662" MajorTopicYN="N">veterinary</QualifierName>
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<DescriptorName UI="D005393" MajorTopicYN="N">Fish Diseases</DescriptorName>
<QualifierName UI="Q000276" MajorTopicYN="Y">immunology</QualifierName>
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<DescriptorName UI="D029941" MajorTopicYN="N">Fish Proteins</DescriptorName>
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<QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName>
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<QualifierName UI="Q000276" MajorTopicYN="Y">immunology</QualifierName>
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<Keyword MajorTopicYN="N">Immune responses</Keyword>
<Keyword MajorTopicYN="N">Redox homeostasis</Keyword>
<Keyword MajorTopicYN="N">Seahorse</Keyword>
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<Year>2019</Year>
<Month>09</Month>
<Day>26</Day>
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<Year>2019</Year>
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<name sortKey="Lee, Jehee" sort="Lee, Jehee" uniqKey="Lee J" first="Jehee" last="Lee">Jehee Lee</name>
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