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...
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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 |
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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 & 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>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16814021$$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 & 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 & 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> |
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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 |
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