Allantopyrone A interferes with multiple components of the TNF receptor 1 complex and blocks RIP1 modifications in the TNF-[alpha]-induced signaling pathway
Allantopyrone A is a fungal metabolite that uniquely possesses two α,β-unsaturated carbonyl moieties. We recently reported that allantopyrone A inhibited the nuclear factor-κB (NF-κB) signaling pathway induced by tumor necrosis factor (TNF)-α in human lung carcinoma A549 cells. In the present study,...
Gespeichert in:
Veröffentlicht in: | Journal of antibiotics 2017-09, Vol.70 (9), p.929 |
---|---|
Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | 9 |
container_start_page | 929 |
container_title | Journal of antibiotics |
container_volume | 70 |
creator | Quach, Hue Tu Tanigaki, Riho Yokoigawa, Junpei Yamada, Yuriko Niwa, Masamitsu Hirano, Seiya Shiono, Yoshihito Kimura, Ken-ichi Kataoka, Takao |
description | Allantopyrone A is a fungal metabolite that uniquely possesses two α,β-unsaturated carbonyl moieties. We recently reported that allantopyrone A inhibited the nuclear factor-κB (NF-κB) signaling pathway induced by tumor necrosis factor (TNF)-α in human lung carcinoma A549 cells. In the present study, the mechanism by which allantopyrone A inhibits the TNF-α-induced signaling pathway was investigated in more detail. Allantopyrone A blocked extensive modifications to receptor-interacting protein 1 (RIP1) in the TNF receptor 1 (TNF-R1) complex. Allantopyrone A augmented the high-MW bands of TNF-R1, TNF receptor-associated factor 2, RIP1, the NF-κB subunit RelA and inhibitor of NF-κB kinase β in A549 cells, suggesting that it binds to and promotes the crosslinking of these proteins. The extracellular cysteine-rich domains of TNF-R1 were crosslinked by allantopyrone A more preferentially than its intracellular portion. The present results demonstrate that allantopyrone A interferes with multiple components of the TNF-R1 complex and blocks RIP1 modifications in the TNF-α-induced NF-κB signaling pathway. |
doi_str_mv | 10.1038/ja.2017.74 |
format | Article |
fullrecord | <record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_journals_1932776268</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1932776268</sourcerecordid><originalsourceid>FETCH-proquest_journals_19327762683</originalsourceid><addsrcrecordid>eNqNzM1KxDAYheEgCtafjVfwgevW_AxNZjmIg25EZHYiQ2y_TlPTJCYp49yLF2sR3bs6m-c9hFwxWjEq1M2gK06ZrOTiiBRMKVayRb08JgWlnJVKcXpKzlIaKBVSSFWQr5W12mUfDtE7hBUYlzF2GDHB3uQexslmEyxC48cwE5cT-A5yj7B5XEPEBkP2EdgPsPgJ2rXwZn3znuD54YnB6FvTmUZn412a___a8kXb0OvX0rh2arCFZHZOW-N2EHTu9_pwQU46bRNe_u45uV7fbW7vyxD9x4Qpbwc_xblJW7YUXMqa10r8T30DLBNgAw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1932776268</pqid></control><display><type>article</type><title>Allantopyrone A interferes with multiple components of the TNF receptor 1 complex and blocks RIP1 modifications in the TNF-[alpha]-induced signaling pathway</title><source>EZB-FREE-00999 freely available EZB journals</source><creator>Quach, Hue Tu ; Tanigaki, Riho ; Yokoigawa, Junpei ; Yamada, Yuriko ; Niwa, Masamitsu ; Hirano, Seiya ; Shiono, Yoshihito ; Kimura, Ken-ichi ; Kataoka, Takao</creator><creatorcontrib>Quach, Hue Tu ; Tanigaki, Riho ; Yokoigawa, Junpei ; Yamada, Yuriko ; Niwa, Masamitsu ; Hirano, Seiya ; Shiono, Yoshihito ; Kimura, Ken-ichi ; Kataoka, Takao</creatorcontrib><description>Allantopyrone A is a fungal metabolite that uniquely possesses two α,β-unsaturated carbonyl moieties. We recently reported that allantopyrone A inhibited the nuclear factor-κB (NF-κB) signaling pathway induced by tumor necrosis factor (TNF)-α in human lung carcinoma A549 cells. In the present study, the mechanism by which allantopyrone A inhibits the TNF-α-induced signaling pathway was investigated in more detail. Allantopyrone A blocked extensive modifications to receptor-interacting protein 1 (RIP1) in the TNF receptor 1 (TNF-R1) complex. Allantopyrone A augmented the high-MW bands of TNF-R1, TNF receptor-associated factor 2, RIP1, the NF-κB subunit RelA and inhibitor of NF-κB kinase β in A549 cells, suggesting that it binds to and promotes the crosslinking of these proteins. The extracellular cysteine-rich domains of TNF-R1 were crosslinked by allantopyrone A more preferentially than its intracellular portion. The present results demonstrate that allantopyrone A interferes with multiple components of the TNF-R1 complex and blocks RIP1 modifications in the TNF-α-induced NF-κB signaling pathway.</description><identifier>ISSN: 0021-8820</identifier><identifier>EISSN: 1881-1469</identifier><identifier>DOI: 10.1038/ja.2017.74</identifier><language>eng</language><publisher>Tokyo: Nature Publishing Group</publisher><subject>Carbonyl compounds ; Kinases ; Metabolites ; T cell receptors ; Tumor necrosis factor-TNF</subject><ispartof>Journal of antibiotics, 2017-09, Vol.70 (9), p.929</ispartof><rights>Copyright Nature Publishing Group Aug 2017</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Quach, Hue Tu</creatorcontrib><creatorcontrib>Tanigaki, Riho</creatorcontrib><creatorcontrib>Yokoigawa, Junpei</creatorcontrib><creatorcontrib>Yamada, Yuriko</creatorcontrib><creatorcontrib>Niwa, Masamitsu</creatorcontrib><creatorcontrib>Hirano, Seiya</creatorcontrib><creatorcontrib>Shiono, Yoshihito</creatorcontrib><creatorcontrib>Kimura, Ken-ichi</creatorcontrib><creatorcontrib>Kataoka, Takao</creatorcontrib><title>Allantopyrone A interferes with multiple components of the TNF receptor 1 complex and blocks RIP1 modifications in the TNF-[alpha]-induced signaling pathway</title><title>Journal of antibiotics</title><description>Allantopyrone A is a fungal metabolite that uniquely possesses two α,β-unsaturated carbonyl moieties. We recently reported that allantopyrone A inhibited the nuclear factor-κB (NF-κB) signaling pathway induced by tumor necrosis factor (TNF)-α in human lung carcinoma A549 cells. In the present study, the mechanism by which allantopyrone A inhibits the TNF-α-induced signaling pathway was investigated in more detail. Allantopyrone A blocked extensive modifications to receptor-interacting protein 1 (RIP1) in the TNF receptor 1 (TNF-R1) complex. Allantopyrone A augmented the high-MW bands of TNF-R1, TNF receptor-associated factor 2, RIP1, the NF-κB subunit RelA and inhibitor of NF-κB kinase β in A549 cells, suggesting that it binds to and promotes the crosslinking of these proteins. The extracellular cysteine-rich domains of TNF-R1 were crosslinked by allantopyrone A more preferentially than its intracellular portion. The present results demonstrate that allantopyrone A interferes with multiple components of the TNF-R1 complex and blocks RIP1 modifications in the TNF-α-induced NF-κB signaling pathway.</description><subject>Carbonyl compounds</subject><subject>Kinases</subject><subject>Metabolites</subject><subject>T cell receptors</subject><subject>Tumor necrosis factor-TNF</subject><issn>0021-8820</issn><issn>1881-1469</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNzM1KxDAYheEgCtafjVfwgevW_AxNZjmIg25EZHYiQ2y_TlPTJCYp49yLF2sR3bs6m-c9hFwxWjEq1M2gK06ZrOTiiBRMKVayRb08JgWlnJVKcXpKzlIaKBVSSFWQr5W12mUfDtE7hBUYlzF2GDHB3uQexslmEyxC48cwE5cT-A5yj7B5XEPEBkP2EdgPsPgJ2rXwZn3znuD54YnB6FvTmUZn412a___a8kXb0OvX0rh2arCFZHZOW-N2EHTu9_pwQU46bRNe_u45uV7fbW7vyxD9x4Qpbwc_xblJW7YUXMqa10r8T30DLBNgAw</recordid><startdate>20170901</startdate><enddate>20170901</enddate><creator>Quach, Hue Tu</creator><creator>Tanigaki, Riho</creator><creator>Yokoigawa, Junpei</creator><creator>Yamada, Yuriko</creator><creator>Niwa, Masamitsu</creator><creator>Hirano, Seiya</creator><creator>Shiono, Yoshihito</creator><creator>Kimura, Ken-ichi</creator><creator>Kataoka, Takao</creator><general>Nature Publishing Group</general><scope>3V.</scope><scope>7QL</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope></search><sort><creationdate>20170901</creationdate><title>Allantopyrone A interferes with multiple components of the TNF receptor 1 complex and blocks RIP1 modifications in the TNF-[alpha]-induced signaling pathway</title><author>Quach, Hue Tu ; Tanigaki, Riho ; Yokoigawa, Junpei ; Yamada, Yuriko ; Niwa, Masamitsu ; Hirano, Seiya ; Shiono, Yoshihito ; Kimura, Ken-ichi ; Kataoka, Takao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_journals_19327762683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Carbonyl compounds</topic><topic>Kinases</topic><topic>Metabolites</topic><topic>T cell receptors</topic><topic>Tumor necrosis factor-TNF</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Quach, Hue Tu</creatorcontrib><creatorcontrib>Tanigaki, Riho</creatorcontrib><creatorcontrib>Yokoigawa, Junpei</creatorcontrib><creatorcontrib>Yamada, Yuriko</creatorcontrib><creatorcontrib>Niwa, Masamitsu</creatorcontrib><creatorcontrib>Hirano, Seiya</creatorcontrib><creatorcontrib>Shiono, Yoshihito</creatorcontrib><creatorcontrib>Kimura, Ken-ichi</creatorcontrib><creatorcontrib>Kataoka, Takao</creatorcontrib><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Immunology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection (ProQuest)</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database (ProQuest)</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><jtitle>Journal of antibiotics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Quach, Hue Tu</au><au>Tanigaki, Riho</au><au>Yokoigawa, Junpei</au><au>Yamada, Yuriko</au><au>Niwa, Masamitsu</au><au>Hirano, Seiya</au><au>Shiono, Yoshihito</au><au>Kimura, Ken-ichi</au><au>Kataoka, Takao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Allantopyrone A interferes with multiple components of the TNF receptor 1 complex and blocks RIP1 modifications in the TNF-[alpha]-induced signaling pathway</atitle><jtitle>Journal of antibiotics</jtitle><date>2017-09-01</date><risdate>2017</risdate><volume>70</volume><issue>9</issue><spage>929</spage><pages>929-</pages><issn>0021-8820</issn><eissn>1881-1469</eissn><abstract>Allantopyrone A is a fungal metabolite that uniquely possesses two α,β-unsaturated carbonyl moieties. We recently reported that allantopyrone A inhibited the nuclear factor-κB (NF-κB) signaling pathway induced by tumor necrosis factor (TNF)-α in human lung carcinoma A549 cells. In the present study, the mechanism by which allantopyrone A inhibits the TNF-α-induced signaling pathway was investigated in more detail. Allantopyrone A blocked extensive modifications to receptor-interacting protein 1 (RIP1) in the TNF receptor 1 (TNF-R1) complex. Allantopyrone A augmented the high-MW bands of TNF-R1, TNF receptor-associated factor 2, RIP1, the NF-κB subunit RelA and inhibitor of NF-κB kinase β in A549 cells, suggesting that it binds to and promotes the crosslinking of these proteins. The extracellular cysteine-rich domains of TNF-R1 were crosslinked by allantopyrone A more preferentially than its intracellular portion. The present results demonstrate that allantopyrone A interferes with multiple components of the TNF-R1 complex and blocks RIP1 modifications in the TNF-α-induced NF-κB signaling pathway.</abstract><cop>Tokyo</cop><pub>Nature Publishing Group</pub><doi>10.1038/ja.2017.74</doi></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0021-8820 |
ispartof | Journal of antibiotics, 2017-09, Vol.70 (9), p.929 |
issn | 0021-8820 1881-1469 |
language | eng |
recordid | cdi_proquest_journals_1932776268 |
source | EZB-FREE-00999 freely available EZB journals |
subjects | Carbonyl compounds Kinases Metabolites T cell receptors Tumor necrosis factor-TNF |
title | Allantopyrone A interferes with multiple components of the TNF receptor 1 complex and blocks RIP1 modifications in the TNF-[alpha]-induced signaling pathway |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T12%3A19%3A56IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Allantopyrone%20A%20interferes%20with%20multiple%20components%20of%20the%20TNF%20receptor%201%20complex%20and%20blocks%20RIP1%20modifications%20in%20the%20TNF-%5Balpha%5D-induced%20signaling%20pathway&rft.jtitle=Journal%20of%20antibiotics&rft.au=Quach,%20Hue%20Tu&rft.date=2017-09-01&rft.volume=70&rft.issue=9&rft.spage=929&rft.pages=929-&rft.issn=0021-8820&rft.eissn=1881-1469&rft_id=info:doi/10.1038/ja.2017.74&rft_dat=%3Cproquest%3E1932776268%3C/proquest%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1932776268&rft_id=info:pmid/&rfr_iscdi=true |