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Augmentation of chemokine production by severe acute respiratory syndrome coronavirus 3a/X1 and 7a/X4 proteins through NF-kappaB activation.

Identifieur interne : 001785 ( Ncbi/Checkpoint ); précédent : 001784; suivant : 001786

Augmentation of chemokine production by severe acute respiratory syndrome coronavirus 3a/X1 and 7a/X4 proteins through NF-kappaB activation.

Auteurs : Noriyuki Kanzawa [Japon] ; Kazuo Nishigaki ; Takaya Hayashi ; Yuichi Ishii ; Souichi Furukawa ; Ayako Niiro ; Fumihiko Yasui ; Michinori Kohara ; Kouichi Morita ; Kouji Matsushima ; Mai Quynh Le ; Takao Masuda ; Mari Kannagi

Source :

RBID : pubmed:17141229

Descripteurs français

English descriptors

Abstract

Severe acute respiratory syndrome (SARS) is characterized by rapidly progressing respiratory failure resembling acute/adult respiratory distress syndrome (ARDS) associated with uncontrolled inflammatory responses. Here, we demonstrated that, among five accessory proteins of SARS coronavirus (SARS-CoV) tested, 3a/X1 and 7a/X4 were capable of activating nuclear factor kappa B (NF-kappaB) and c-Jun N-terminal kinase (JNK), and significantly enhanced interleukin 8 (IL-8) promoter activity. Furthermore, 3a/X1 and 7a/X4 expression in A549 cells enhanced production of inflammatory chemokines that were known to be up-regulated in SARS-CoV infection. Our results suggest potential involvement of 3a/X1 and 7a/X4 proteins in the pathological inflammatory responses in SARS.

DOI: 10.1016/j.febslet.2006.11.046
PubMed: 17141229


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pubmed:17141229

Le document en format XML

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<nlm:affiliation>Department of Immunotherapeutics, Tokyo Medical and Dental University, Graduate School, 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8519, Japan.</nlm:affiliation>
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<name sortKey="Yasui, Fumihiko" sort="Yasui, Fumihiko" uniqKey="Yasui F" first="Fumihiko" last="Yasui">Fumihiko Yasui</name>
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<name sortKey="Hayashi, Takaya" sort="Hayashi, Takaya" uniqKey="Hayashi T" first="Takaya" last="Hayashi">Takaya Hayashi</name>
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<name sortKey="Ishii, Yuichi" sort="Ishii, Yuichi" uniqKey="Ishii Y" first="Yuichi" last="Ishii">Yuichi Ishii</name>
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<name sortKey="Furukawa, Souichi" sort="Furukawa, Souichi" uniqKey="Furukawa S" first="Souichi" last="Furukawa">Souichi Furukawa</name>
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<name sortKey="Yasui, Fumihiko" sort="Yasui, Fumihiko" uniqKey="Yasui F" first="Fumihiko" last="Yasui">Fumihiko Yasui</name>
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<name sortKey="Kohara, Michinori" sort="Kohara, Michinori" uniqKey="Kohara M" first="Michinori" last="Kohara">Michinori Kohara</name>
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<name sortKey="Matsushima, Kouji" sort="Matsushima, Kouji" uniqKey="Matsushima K" first="Kouji" last="Matsushima">Kouji Matsushima</name>
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<name sortKey="Le, Mai Quynh" sort="Le, Mai Quynh" uniqKey="Le M" first="Mai Quynh" last="Le">Mai Quynh Le</name>
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<name sortKey="Masuda, Takao" sort="Masuda, Takao" uniqKey="Masuda T" first="Takao" last="Masuda">Takao Masuda</name>
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<term>Cell Line</term>
<term>Chemokines (biosynthesis)</term>
<term>Enzyme Activation</term>
<term>Gene Expression</term>
<term>Humans</term>
<term>JNK Mitogen-Activated Protein Kinases (metabolism)</term>
<term>NF-kappa B (metabolism)</term>
<term>Promoter Regions, Genetic (genetics)</term>
<term>SARS Virus (genetics)</term>
<term>SARS Virus (metabolism)</term>
<term>Viral Matrix Proteins (genetics)</term>
<term>Viral Matrix Proteins (metabolism)</term>
<term>Viral Proteins (genetics)</term>
<term>Viral Proteins (metabolism)</term>
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<term>Viral Structural Proteins (metabolism)</term>
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<term>Activation enzymatique</term>
<term>Chimiokines (biosynthèse)</term>
<term>Expression des gènes</term>
<term>Facteur de transcription NF-kappa B (métabolisme)</term>
<term>Humains</term>
<term>JNK Mitogen-Activated Protein Kinases (métabolisme)</term>
<term>Lignée cellulaire</term>
<term>Protéines de la matrice virale (génétique)</term>
<term>Protéines de la matrice virale (métabolisme)</term>
<term>Protéines virales (génétique)</term>
<term>Protéines virales (métabolisme)</term>
<term>Protéines virales structurales (génétique)</term>
<term>Protéines virales structurales (métabolisme)</term>
<term>Régions promotrices (génétique) (génétique)</term>
<term>Virus du SRAS (génétique)</term>
<term>Virus du SRAS (métabolisme)</term>
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<term>Chemokines</term>
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<term>Viral Matrix Proteins</term>
<term>Viral Proteins</term>
<term>Viral Structural Proteins</term>
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<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en">
<term>JNK Mitogen-Activated Protein Kinases</term>
<term>NF-kappa B</term>
<term>Viral Matrix Proteins</term>
<term>Viral Proteins</term>
<term>Viral Structural Proteins</term>
</keywords>
<keywords scheme="MESH" qualifier="biosynthèse" xml:lang="fr">
<term>Chimiokines</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>Promoter Regions, Genetic</term>
<term>SARS Virus</term>
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<keywords scheme="MESH" qualifier="génétique" xml:lang="fr">
<term>Protéines de la matrice virale</term>
<term>Protéines virales</term>
<term>Protéines virales structurales</term>
<term>Régions promotrices (génétique)</term>
<term>Virus du SRAS</term>
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<keywords scheme="MESH" qualifier="metabolism" xml:lang="en">
<term>SARS Virus</term>
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<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr">
<term>Facteur de transcription NF-kappa B</term>
<term>JNK Mitogen-Activated Protein Kinases</term>
<term>Protéines de la matrice virale</term>
<term>Protéines virales</term>
<term>Protéines virales structurales</term>
<term>Virus du SRAS</term>
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<term>Enzyme Activation</term>
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<div type="abstract" xml:lang="en">Severe acute respiratory syndrome (SARS) is characterized by rapidly progressing respiratory failure resembling acute/adult respiratory distress syndrome (ARDS) associated with uncontrolled inflammatory responses. Here, we demonstrated that, among five accessory proteins of SARS coronavirus (SARS-CoV) tested, 3a/X1 and 7a/X4 were capable of activating nuclear factor kappa B (NF-kappaB) and c-Jun N-terminal kinase (JNK), and significantly enhanced interleukin 8 (IL-8) promoter activity. Furthermore, 3a/X1 and 7a/X4 expression in A549 cells enhanced production of inflammatory chemokines that were known to be up-regulated in SARS-CoV infection. Our results suggest potential involvement of 3a/X1 and 7a/X4 proteins in the pathological inflammatory responses in SARS.</div>
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<name sortKey="Matsushima, Kouji" sort="Matsushima, Kouji" uniqKey="Matsushima K" first="Kouji" last="Matsushima">Kouji Matsushima</name>
<name sortKey="Morita, Kouichi" sort="Morita, Kouichi" uniqKey="Morita K" first="Kouichi" last="Morita">Kouichi Morita</name>
<name sortKey="Niiro, Ayako" sort="Niiro, Ayako" uniqKey="Niiro A" first="Ayako" last="Niiro">Ayako Niiro</name>
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<name sortKey="Kanzawa, Noriyuki" sort="Kanzawa, Noriyuki" uniqKey="Kanzawa N" first="Noriyuki" last="Kanzawa">Noriyuki Kanzawa</name>
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