Dioscorin isolated from Dioscorea alata activates TLR4-signaling pathways and induces cytokine expression in macrophages
The Toll-like receptor 4 (TLR4)-signaling pathway is crucial for activating both innate and adaptive immunity. TLR4 is a promising molecular target for immune-modulating drugs, and TLR4 agonists are of therapeutic potential for treating immune diseases and cancers. Several medicinal herb-derived com...
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Veröffentlicht in: | Biochemical and biophysical research communications 2006-01, Vol.339 (1), p.137-144 |
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description | The Toll-like receptor 4 (TLR4)-signaling pathway is crucial for activating both innate and adaptive immunity. TLR4 is a promising molecular target for immune-modulating drugs, and TLR4 agonists are of therapeutic potential for treating immune diseases and cancers. Several medicinal herb-derived components have recently been reported to act via TLR4-dependent pathways, suggesting that medicinal plants are potential resources for identifying TLR4 activators. We have applied a screening procedure to systematically identify herbal constituents that activate TLR4. To exclude possible LPS contamination in these plant-derived components, a LPS inhibitor, polymyxin B, was added during screening. One of the plant components we identified from the screening was dioscorin, the glycoprotein isolated from
Dioscorea alata. It induced TLR4-downstream cytokine expression in bone marrow cells isolated from TLR4-functional C3H/HeN mice but not from TLR4-defective C3H/HeJ mice. Dioscorin also stimulated multiple signaling molecules (NF-κB, ERK, JNK, and p38) and induced the expression of cytokines (TNF-α, IL-1β, and IL-6) in murine RAW 264.7 macrophages. Furthermore, the ERK, p38, JNK, and NF-κB-mediated pathways are all involved in dioscorin-mediated TNF-α production. In summary, our results demonstrate that dioscorin is a novel TLR4 activator and induces macrophage activation via typical TLR4-signaling pathways. |
doi_str_mv | 10.1016/j.bbrc.2005.11.005 |
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Dioscorea alata. It induced TLR4-downstream cytokine expression in bone marrow cells isolated from TLR4-functional C3H/HeN mice but not from TLR4-defective C3H/HeJ mice. Dioscorin also stimulated multiple signaling molecules (NF-κB, ERK, JNK, and p38) and induced the expression of cytokines (TNF-α, IL-1β, and IL-6) in murine RAW 264.7 macrophages. Furthermore, the ERK, p38, JNK, and NF-κB-mediated pathways are all involved in dioscorin-mediated TNF-α production. In summary, our results demonstrate that dioscorin is a novel TLR4 activator and induces macrophage activation via typical TLR4-signaling pathways.</description><identifier>ISSN: 0006-291X</identifier><identifier>EISSN: 1090-2104</identifier><identifier>DOI: 10.1016/j.bbrc.2005.11.005</identifier><identifier>PMID: 16297883</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Bone Marrow Cells - drug effects ; Bone Marrow Cells - physiology ; Cells, Cultured ; Cytokine ; Cytokines - metabolism ; Dioscorea - chemistry ; Dioscorea alata ; Dioscorin ; Glycoproteins - isolation & purification ; Glycoproteins - pharmacology ; JNK Mitogen-Activated Protein Kinases - metabolism ; Lipopolysaccharides - pharmacology ; Macrophages - drug effects ; Macrophages - metabolism ; MAP Kinase Signaling System - physiology ; MAPK ; Mice ; NF-kappa B - metabolism ; NF-κB ; Plant Extracts - isolation & purification ; Plant Extracts - pharmacology ; Polymyxin B - pharmacology ; Signal Transduction ; TLR4 ; Toll-Like Receptor 4 - agonists ; Toll-Like Receptor 4 - physiology ; Tumor Necrosis Factor-alpha - metabolism</subject><ispartof>Biochemical and biophysical research communications, 2006-01, Vol.339 (1), p.137-144</ispartof><rights>2005 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c464t-3b4edc4cefbca1208f6d75bddb5748f8fe068ccf5d1e1da9b512227dd5cecf843</citedby><cites>FETCH-LOGICAL-c464t-3b4edc4cefbca1208f6d75bddb5748f8fe068ccf5d1e1da9b512227dd5cecf843</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.bbrc.2005.11.005$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16297883$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fu, Shu-Ling</creatorcontrib><creatorcontrib>Hsu, Ya-Hui</creatorcontrib><creatorcontrib>Lee, Pei-Yeh</creatorcontrib><creatorcontrib>Hou, Wen-Chi</creatorcontrib><creatorcontrib>Hung, Ling-Chien</creatorcontrib><creatorcontrib>Lin, Chao-Hsiung</creatorcontrib><creatorcontrib>Chen, Chiu-Ming</creatorcontrib><creatorcontrib>Huang, Yu-Jing</creatorcontrib><title>Dioscorin isolated from Dioscorea alata activates TLR4-signaling pathways and induces cytokine expression in macrophages</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><description>The Toll-like receptor 4 (TLR4)-signaling pathway is crucial for activating both innate and adaptive immunity. TLR4 is a promising molecular target for immune-modulating drugs, and TLR4 agonists are of therapeutic potential for treating immune diseases and cancers. Several medicinal herb-derived components have recently been reported to act via TLR4-dependent pathways, suggesting that medicinal plants are potential resources for identifying TLR4 activators. We have applied a screening procedure to systematically identify herbal constituents that activate TLR4. To exclude possible LPS contamination in these plant-derived components, a LPS inhibitor, polymyxin B, was added during screening. One of the plant components we identified from the screening was dioscorin, the glycoprotein isolated from
Dioscorea alata. It induced TLR4-downstream cytokine expression in bone marrow cells isolated from TLR4-functional C3H/HeN mice but not from TLR4-defective C3H/HeJ mice. Dioscorin also stimulated multiple signaling molecules (NF-κB, ERK, JNK, and p38) and induced the expression of cytokines (TNF-α, IL-1β, and IL-6) in murine RAW 264.7 macrophages. Furthermore, the ERK, p38, JNK, and NF-κB-mediated pathways are all involved in dioscorin-mediated TNF-α production. In summary, our results demonstrate that dioscorin is a novel TLR4 activator and induces macrophage activation via typical TLR4-signaling pathways.</description><subject>Animals</subject><subject>Bone Marrow Cells - drug effects</subject><subject>Bone Marrow Cells - physiology</subject><subject>Cells, Cultured</subject><subject>Cytokine</subject><subject>Cytokines - metabolism</subject><subject>Dioscorea - chemistry</subject><subject>Dioscorea alata</subject><subject>Dioscorin</subject><subject>Glycoproteins - isolation & purification</subject><subject>Glycoproteins - pharmacology</subject><subject>JNK Mitogen-Activated Protein Kinases - metabolism</subject><subject>Lipopolysaccharides - pharmacology</subject><subject>Macrophages - drug effects</subject><subject>Macrophages - metabolism</subject><subject>MAP Kinase Signaling System - physiology</subject><subject>MAPK</subject><subject>Mice</subject><subject>NF-kappa B - metabolism</subject><subject>NF-κB</subject><subject>Plant Extracts - isolation & purification</subject><subject>Plant Extracts - pharmacology</subject><subject>Polymyxin B - pharmacology</subject><subject>Signal Transduction</subject><subject>TLR4</subject><subject>Toll-Like Receptor 4 - agonists</subject><subject>Toll-Like Receptor 4 - physiology</subject><subject>Tumor Necrosis Factor-alpha - metabolism</subject><issn>0006-291X</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1rGzEQhkVpaNy0f6CHolNvu9XI2i_opST9AkMgJNCb0I5Gjtzd1VZap_G_r4wNvfUyL8w88zLzMvYORAkC6o-7su8jllKIqgQos7xgKxCdKCQI9ZKthBB1ITv4eclep7QTAkDV3St2CbXsmrZdr9jzjQ8JQ_QT9ykMZiHLXQwjP_fJcJO7ueLin_I48fvNnSqS305m8NOWz2Z5_GMOiZvJcj_ZPWYGD0v45Sfi9DxHSsmH7D_x0WAM86PZUnrDLpwZEr096xV7-Prl_vp7sbn99uP686ZAVaulWPeKLCok16MBKVpX26bqre2rRrWudSTqFtFVFgis6foKpJSNtRUSulatr9iHk-8cw-89pUWPPiENg5ko7JNuBHRNpaoMyhOYT0wpktNz9KOJBw1CH_PWO33MWx_z1gA6S156f3bf9yPZfyvngDPw6QRQ_vHJU9QJPU1I1kfCRdvg_-f_F0welXE</recordid><startdate>20060106</startdate><enddate>20060106</enddate><creator>Fu, Shu-Ling</creator><creator>Hsu, Ya-Hui</creator><creator>Lee, Pei-Yeh</creator><creator>Hou, Wen-Chi</creator><creator>Hung, Ling-Chien</creator><creator>Lin, Chao-Hsiung</creator><creator>Chen, Chiu-Ming</creator><creator>Huang, Yu-Jing</creator><general>Elsevier Inc</general><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>7X8</scope></search><sort><creationdate>20060106</creationdate><title>Dioscorin isolated from Dioscorea alata activates TLR4-signaling pathways and induces cytokine expression in macrophages</title><author>Fu, Shu-Ling ; Hsu, Ya-Hui ; Lee, Pei-Yeh ; Hou, Wen-Chi ; Hung, Ling-Chien ; Lin, Chao-Hsiung ; Chen, Chiu-Ming ; Huang, Yu-Jing</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c464t-3b4edc4cefbca1208f6d75bddb5748f8fe068ccf5d1e1da9b512227dd5cecf843</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>Bone Marrow Cells - drug effects</topic><topic>Bone Marrow Cells - physiology</topic><topic>Cells, Cultured</topic><topic>Cytokine</topic><topic>Cytokines - metabolism</topic><topic>Dioscorea - chemistry</topic><topic>Dioscorea alata</topic><topic>Dioscorin</topic><topic>Glycoproteins - isolation & purification</topic><topic>Glycoproteins - pharmacology</topic><topic>JNK Mitogen-Activated Protein Kinases - metabolism</topic><topic>Lipopolysaccharides - pharmacology</topic><topic>Macrophages - drug effects</topic><topic>Macrophages - metabolism</topic><topic>MAP Kinase Signaling System - physiology</topic><topic>MAPK</topic><topic>Mice</topic><topic>NF-kappa B - metabolism</topic><topic>NF-κB</topic><topic>Plant Extracts - isolation & purification</topic><topic>Plant Extracts - pharmacology</topic><topic>Polymyxin B - pharmacology</topic><topic>Signal Transduction</topic><topic>TLR4</topic><topic>Toll-Like Receptor 4 - agonists</topic><topic>Toll-Like Receptor 4 - physiology</topic><topic>Tumor Necrosis Factor-alpha - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fu, Shu-Ling</creatorcontrib><creatorcontrib>Hsu, Ya-Hui</creatorcontrib><creatorcontrib>Lee, Pei-Yeh</creatorcontrib><creatorcontrib>Hou, Wen-Chi</creatorcontrib><creatorcontrib>Hung, Ling-Chien</creatorcontrib><creatorcontrib>Lin, Chao-Hsiung</creatorcontrib><creatorcontrib>Chen, Chiu-Ming</creatorcontrib><creatorcontrib>Huang, Yu-Jing</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Biochemical and biophysical research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fu, Shu-Ling</au><au>Hsu, Ya-Hui</au><au>Lee, Pei-Yeh</au><au>Hou, Wen-Chi</au><au>Hung, Ling-Chien</au><au>Lin, Chao-Hsiung</au><au>Chen, Chiu-Ming</au><au>Huang, Yu-Jing</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dioscorin isolated from Dioscorea alata activates TLR4-signaling pathways and induces cytokine expression in macrophages</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>2006-01-06</date><risdate>2006</risdate><volume>339</volume><issue>1</issue><spage>137</spage><epage>144</epage><pages>137-144</pages><issn>0006-291X</issn><eissn>1090-2104</eissn><abstract>The Toll-like receptor 4 (TLR4)-signaling pathway is crucial for activating both innate and adaptive immunity. TLR4 is a promising molecular target for immune-modulating drugs, and TLR4 agonists are of therapeutic potential for treating immune diseases and cancers. Several medicinal herb-derived components have recently been reported to act via TLR4-dependent pathways, suggesting that medicinal plants are potential resources for identifying TLR4 activators. We have applied a screening procedure to systematically identify herbal constituents that activate TLR4. To exclude possible LPS contamination in these plant-derived components, a LPS inhibitor, polymyxin B, was added during screening. One of the plant components we identified from the screening was dioscorin, the glycoprotein isolated from
Dioscorea alata. It induced TLR4-downstream cytokine expression in bone marrow cells isolated from TLR4-functional C3H/HeN mice but not from TLR4-defective C3H/HeJ mice. Dioscorin also stimulated multiple signaling molecules (NF-κB, ERK, JNK, and p38) and induced the expression of cytokines (TNF-α, IL-1β, and IL-6) in murine RAW 264.7 macrophages. Furthermore, the ERK, p38, JNK, and NF-κB-mediated pathways are all involved in dioscorin-mediated TNF-α production. In summary, our results demonstrate that dioscorin is a novel TLR4 activator and induces macrophage activation via typical TLR4-signaling pathways.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>16297883</pmid><doi>10.1016/j.bbrc.2005.11.005</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Bone Marrow Cells - drug effects Bone Marrow Cells - physiology Cells, Cultured Cytokine Cytokines - metabolism Dioscorea - chemistry Dioscorea alata Dioscorin Glycoproteins - isolation & purification Glycoproteins - pharmacology JNK Mitogen-Activated Protein Kinases - metabolism Lipopolysaccharides - pharmacology Macrophages - drug effects Macrophages - metabolism MAP Kinase Signaling System - physiology MAPK Mice NF-kappa B - metabolism NF-κB Plant Extracts - isolation & purification Plant Extracts - pharmacology Polymyxin B - pharmacology Signal Transduction TLR4 Toll-Like Receptor 4 - agonists Toll-Like Receptor 4 - physiology Tumor Necrosis Factor-alpha - metabolism |
title | Dioscorin isolated from Dioscorea alata activates TLR4-signaling pathways and induces cytokine expression in macrophages |
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