Macrophage activation by polysaccharide isolated from Astragalus membranaceus

We show that APS, a polysaccharide isolated from the roots of Astragalus membranaceus, significantly induces nitric oxide (NO) production and inducible NO synthase (iNOS) transcription through the activation of nuclear factor-κB/Rel (NF-κB/Rel). In vivo administration of APS induced NO production by...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:International immunopharmacology 2005-07, Vol.5 (7), p.1225-1233
Hauptverfasser: Lee, Kun Yeong, Jeon, Young Jin
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1233
container_issue 7
container_start_page 1225
container_title International immunopharmacology
container_volume 5
creator Lee, Kun Yeong
Jeon, Young Jin
description We show that APS, a polysaccharide isolated from the roots of Astragalus membranaceus, significantly induces nitric oxide (NO) production and inducible NO synthase (iNOS) transcription through the activation of nuclear factor-κB/Rel (NF-κB/Rel). In vivo administration of APS induced NO production by peritoneal macrophages of B6C3F1 mice. APS also dose-dependently induced the production of NO in isolated mouse peritoneal macrophages and RAW 264.7, a mouse macrophage-like cell line. Moreover, iNOS protein and mRNA transcription were strongly induced by APS in RAW 264.7 cells. To further investigate the mechanism responsible for the induction of iNOS gene expression, we investigated the effect of APS on the activation of transcription factors including NF-κB/Rel and Oct, whose binding sites were located in the promoter of iNOS gene. Treatment of RAW 264.7 cells with APS produced strong induction of NF-κB/Rel-dependent reporter gene expression, whereas Oct-dependent gene expression was not affected by APS. Nuclear translocation and DNA binding activity of NF-κB/Rel was significantly induced by APS. The treatment with NF-κB SN50, an inhibitor of NF-κB/Rel nuclear translocation, effectively inhibited the activation of NF-κB/Rel binding complexes and NO production. In conclusion, we demonstrate that APS stimulates macrophages to express iNOS gene through the activation of NF-κB/Rel.
doi_str_mv 10.1016/j.intimp.2005.02.020
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_67868399</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1567576905000688</els_id><sourcerecordid>67868399</sourcerecordid><originalsourceid>FETCH-LOGICAL-c487t-58f567e694f609eb0055ecfe389b3850b8d34be0438d3041e3820f0d4726b823</originalsourceid><addsrcrecordid>eNqFkEtLxDAQgIMouq7-A5Fe9NZ10ubViyCLL1jx4j2k6VSz9GXSLuy_N8sueFMYyJB888hHyBWFBQUq7tYL142uHRYZAF9AFgOOyIwqqVIqgR_HnAuZcimKM3Iewhog3jN6Ss4oLyjLMzkjb2_G-n74Mp-YGDu6jRld3yXlNhn6ZhuMtV_GuwoTF_rGjFglte_b5CGM3nyaZgpJi23pTWcsTuGCnNSmCXh5OOfk4-nxY_mSrt6fX5cPq9QyJceUqzpuhqJgtYACy_gBjrbGXBVlrjiUqspZicDymMSN40MGNVRMZqJUWT4nt_u2g--_Jwyjbl2w2DSmw34KWkglVF4U_4JUMi55nDMnbA9GGSF4rPXgXWv8VlPQO916rfe69U63hiwGxLLrQ_-pbLH6LTr4jcDNATDBmqaOoqwLv5xQlEFGI3e_5zBa2zj0OliHncXKebSjrnr39yY_ScGftw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>17457504</pqid></control><display><type>article</type><title>Macrophage activation by polysaccharide isolated from Astragalus membranaceus</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Lee, Kun Yeong ; Jeon, Young Jin</creator><creatorcontrib>Lee, Kun Yeong ; Jeon, Young Jin</creatorcontrib><description>We show that APS, a polysaccharide isolated from the roots of Astragalus membranaceus, significantly induces nitric oxide (NO) production and inducible NO synthase (iNOS) transcription through the activation of nuclear factor-κB/Rel (NF-κB/Rel). In vivo administration of APS induced NO production by peritoneal macrophages of B6C3F1 mice. APS also dose-dependently induced the production of NO in isolated mouse peritoneal macrophages and RAW 264.7, a mouse macrophage-like cell line. Moreover, iNOS protein and mRNA transcription were strongly induced by APS in RAW 264.7 cells. To further investigate the mechanism responsible for the induction of iNOS gene expression, we investigated the effect of APS on the activation of transcription factors including NF-κB/Rel and Oct, whose binding sites were located in the promoter of iNOS gene. Treatment of RAW 264.7 cells with APS produced strong induction of NF-κB/Rel-dependent reporter gene expression, whereas Oct-dependent gene expression was not affected by APS. Nuclear translocation and DNA binding activity of NF-κB/Rel was significantly induced by APS. The treatment with NF-κB SN50, an inhibitor of NF-κB/Rel nuclear translocation, effectively inhibited the activation of NF-κB/Rel binding complexes and NO production. In conclusion, we demonstrate that APS stimulates macrophages to express iNOS gene through the activation of NF-κB/Rel.</description><identifier>ISSN: 1567-5769</identifier><identifier>EISSN: 1878-1705</identifier><identifier>DOI: 10.1016/j.intimp.2005.02.020</identifier><identifier>PMID: 15914327</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Active Transport, Cell Nucleus - drug effects ; Animals ; Astragalus membranaceus ; Astragalus membranaceus - chemistry ; Biological and medical sciences ; Cell Line ; Female ; Gene Expression Regulation, Enzymologic - drug effects ; iNOS ; Macrophage Activation - drug effects ; Macrophages ; Medical sciences ; Mice ; NF-kappa B - antagonists &amp; inhibitors ; NF-kappa B - metabolism ; NF-κB/Rel ; Nitric Oxide - biosynthesis ; Nitric Oxide Synthase - genetics ; Nitric Oxide Synthase Type II ; Nitrites - metabolism ; Pharmacology. Drug treatments ; Polymyxin B - pharmacology ; Polysaccharides - pharmacology</subject><ispartof>International immunopharmacology, 2005-07, Vol.5 (7), p.1225-1233</ispartof><rights>2005 Elsevier B.V.</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c487t-58f567e694f609eb0055ecfe389b3850b8d34be0438d3041e3820f0d4726b823</citedby><cites>FETCH-LOGICAL-c487t-58f567e694f609eb0055ecfe389b3850b8d34be0438d3041e3820f0d4726b823</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1567576905000688$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27902,27903,65308</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=16814021$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15914327$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, Kun Yeong</creatorcontrib><creatorcontrib>Jeon, Young Jin</creatorcontrib><title>Macrophage activation by polysaccharide isolated from Astragalus membranaceus</title><title>International immunopharmacology</title><addtitle>Int Immunopharmacol</addtitle><description>We show that APS, a polysaccharide isolated from the roots of Astragalus membranaceus, significantly induces nitric oxide (NO) production and inducible NO synthase (iNOS) transcription through the activation of nuclear factor-κB/Rel (NF-κB/Rel). In vivo administration of APS induced NO production by peritoneal macrophages of B6C3F1 mice. APS also dose-dependently induced the production of NO in isolated mouse peritoneal macrophages and RAW 264.7, a mouse macrophage-like cell line. Moreover, iNOS protein and mRNA transcription were strongly induced by APS in RAW 264.7 cells. To further investigate the mechanism responsible for the induction of iNOS gene expression, we investigated the effect of APS on the activation of transcription factors including NF-κB/Rel and Oct, whose binding sites were located in the promoter of iNOS gene. Treatment of RAW 264.7 cells with APS produced strong induction of NF-κB/Rel-dependent reporter gene expression, whereas Oct-dependent gene expression was not affected by APS. Nuclear translocation and DNA binding activity of NF-κB/Rel was significantly induced by APS. The treatment with NF-κB SN50, an inhibitor of NF-κB/Rel nuclear translocation, effectively inhibited the activation of NF-κB/Rel binding complexes and NO production. In conclusion, we demonstrate that APS stimulates macrophages to express iNOS gene through the activation of NF-κB/Rel.</description><subject>Active Transport, Cell Nucleus - drug effects</subject><subject>Animals</subject><subject>Astragalus membranaceus</subject><subject>Astragalus membranaceus - chemistry</subject><subject>Biological and medical sciences</subject><subject>Cell Line</subject><subject>Female</subject><subject>Gene Expression Regulation, Enzymologic - drug effects</subject><subject>iNOS</subject><subject>Macrophage Activation - drug effects</subject><subject>Macrophages</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>NF-kappa B - antagonists &amp; inhibitors</subject><subject>NF-kappa B - metabolism</subject><subject>NF-κB/Rel</subject><subject>Nitric Oxide - biosynthesis</subject><subject>Nitric Oxide Synthase - genetics</subject><subject>Nitric Oxide Synthase Type II</subject><subject>Nitrites - metabolism</subject><subject>Pharmacology. Drug treatments</subject><subject>Polymyxin B - pharmacology</subject><subject>Polysaccharides - pharmacology</subject><issn>1567-5769</issn><issn>1878-1705</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtLxDAQgIMouq7-A5Fe9NZ10ubViyCLL1jx4j2k6VSz9GXSLuy_N8sueFMYyJB888hHyBWFBQUq7tYL142uHRYZAF9AFgOOyIwqqVIqgR_HnAuZcimKM3Iewhog3jN6Ss4oLyjLMzkjb2_G-n74Mp-YGDu6jRld3yXlNhn6ZhuMtV_GuwoTF_rGjFglte_b5CGM3nyaZgpJi23pTWcsTuGCnNSmCXh5OOfk4-nxY_mSrt6fX5cPq9QyJceUqzpuhqJgtYACy_gBjrbGXBVlrjiUqspZicDymMSN40MGNVRMZqJUWT4nt_u2g--_Jwyjbl2w2DSmw34KWkglVF4U_4JUMi55nDMnbA9GGSF4rPXgXWv8VlPQO916rfe69U63hiwGxLLrQ_-pbLH6LTr4jcDNATDBmqaOoqwLv5xQlEFGI3e_5zBa2zj0OliHncXKebSjrnr39yY_ScGftw</recordid><startdate>20050701</startdate><enddate>20050701</enddate><creator>Lee, Kun Yeong</creator><creator>Jeon, Young Jin</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><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></search><sort><creationdate>20050701</creationdate><title>Macrophage activation by polysaccharide isolated from Astragalus membranaceus</title><author>Lee, Kun Yeong ; Jeon, Young Jin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c487t-58f567e694f609eb0055ecfe389b3850b8d34be0438d3041e3820f0d4726b823</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Active Transport, Cell Nucleus - drug effects</topic><topic>Animals</topic><topic>Astragalus membranaceus</topic><topic>Astragalus membranaceus - chemistry</topic><topic>Biological and medical sciences</topic><topic>Cell Line</topic><topic>Female</topic><topic>Gene Expression Regulation, Enzymologic - drug effects</topic><topic>iNOS</topic><topic>Macrophage Activation - drug effects</topic><topic>Macrophages</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>NF-kappa B - antagonists &amp; inhibitors</topic><topic>NF-kappa B - metabolism</topic><topic>NF-κB/Rel</topic><topic>Nitric Oxide - biosynthesis</topic><topic>Nitric Oxide Synthase - genetics</topic><topic>Nitric Oxide Synthase Type II</topic><topic>Nitrites - metabolism</topic><topic>Pharmacology. Drug treatments</topic><topic>Polymyxin B - pharmacology</topic><topic>Polysaccharides - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Kun Yeong</creatorcontrib><creatorcontrib>Jeon, Young Jin</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>International immunopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Kun Yeong</au><au>Jeon, Young Jin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Macrophage activation by polysaccharide isolated from Astragalus membranaceus</atitle><jtitle>International immunopharmacology</jtitle><addtitle>Int Immunopharmacol</addtitle><date>2005-07-01</date><risdate>2005</risdate><volume>5</volume><issue>7</issue><spage>1225</spage><epage>1233</epage><pages>1225-1233</pages><issn>1567-5769</issn><eissn>1878-1705</eissn><abstract>We show that APS, a polysaccharide isolated from the roots of Astragalus membranaceus, significantly induces nitric oxide (NO) production and inducible NO synthase (iNOS) transcription through the activation of nuclear factor-κB/Rel (NF-κB/Rel). In vivo administration of APS induced NO production by peritoneal macrophages of B6C3F1 mice. APS also dose-dependently induced the production of NO in isolated mouse peritoneal macrophages and RAW 264.7, a mouse macrophage-like cell line. Moreover, iNOS protein and mRNA transcription were strongly induced by APS in RAW 264.7 cells. To further investigate the mechanism responsible for the induction of iNOS gene expression, we investigated the effect of APS on the activation of transcription factors including NF-κB/Rel and Oct, whose binding sites were located in the promoter of iNOS gene. Treatment of RAW 264.7 cells with APS produced strong induction of NF-κB/Rel-dependent reporter gene expression, whereas Oct-dependent gene expression was not affected by APS. Nuclear translocation and DNA binding activity of NF-κB/Rel was significantly induced by APS. The treatment with NF-κB SN50, an inhibitor of NF-κB/Rel nuclear translocation, effectively inhibited the activation of NF-κB/Rel binding complexes and NO production. In conclusion, we demonstrate that APS stimulates macrophages to express iNOS gene through the activation of NF-κB/Rel.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>15914327</pmid><doi>10.1016/j.intimp.2005.02.020</doi><tpages>9</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1567-5769
ispartof International immunopharmacology, 2005-07, Vol.5 (7), p.1225-1233
issn 1567-5769
1878-1705
language eng
recordid cdi_proquest_miscellaneous_67868399
source MEDLINE; Elsevier ScienceDirect Journals
subjects Active Transport, Cell Nucleus - drug effects
Animals
Astragalus membranaceus
Astragalus membranaceus - chemistry
Biological and medical sciences
Cell Line
Female
Gene Expression Regulation, Enzymologic - drug effects
iNOS
Macrophage Activation - drug effects
Macrophages
Medical sciences
Mice
NF-kappa B - antagonists & inhibitors
NF-kappa B - metabolism
NF-κB/Rel
Nitric Oxide - biosynthesis
Nitric Oxide Synthase - genetics
Nitric Oxide Synthase Type II
Nitrites - metabolism
Pharmacology. Drug treatments
Polymyxin B - pharmacology
Polysaccharides - pharmacology
title Macrophage activation by polysaccharide isolated from Astragalus membranaceus
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T09%3A27%3A16IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Macrophage%20activation%20by%20polysaccharide%20isolated%20from%20Astragalus%20membranaceus&rft.jtitle=International%20immunopharmacology&rft.au=Lee,%20Kun%20Yeong&rft.date=2005-07-01&rft.volume=5&rft.issue=7&rft.spage=1225&rft.epage=1233&rft.pages=1225-1233&rft.issn=1567-5769&rft.eissn=1878-1705&rft_id=info:doi/10.1016/j.intimp.2005.02.020&rft_dat=%3Cproquest_cross%3E67868399%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=17457504&rft_id=info:pmid/15914327&rft_els_id=S1567576905000688&rfr_iscdi=true