A polysaccharide purified from Radix Adenophorae promotes cell activation and pro-inflammatory cytokine production in murine RAW264.7 macrophages
Radix Adenophorae, a traditional Chinese medicine, has been reported to have a variety of biological functions. In the present study, a polysaccharide component, Radix Adenophorae Polysaccharide (RAPS), was purified from Radix Adenophorae by decoloring with ADS-7 macroporous adsorption resin, DEAE-5...
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description | Radix Adenophorae, a traditional Chinese medicine, has been reported to have a variety of biological functions. In the present study, a polysaccharide component, Radix Adenophorae Polysaccharide (RAPS), was purified from Radix Adenophorae by decoloring with ADS-7 macroporous adsorption resin, DEAE-52 cellulose ion-exchange chromatography, and Sephacryl S-300HR gel chromatography, with the purity of 98.3% and a molecular weight of 1.8 × 104 Da. The cell viability assay and microscopic examination revealed that RAPS promoted the proliferation and activation of macrophages. At 400 μg·mL-1, RAPS stimulated RAW264.7 cell proliferation by 1.91-fold compared with the control. Meanwhile, RAPS significantly increased the secretion of pro-inflammatory cytokines (TNF-a and IL-6) in a dose-dependent manner in the supernatant of RAW264.7 cell culture as determined by ELISA. At 400 μg·mL-1, the production of TNF-a was 20.8-fold higher than that of the control. Simultaneously, the production of nitric oxide (NO) and the expression of inducible nitric oxide synthase (iNOS) were increased in RAW264.7 cells incubated with RAPS, as measured by Griess assay and Western blot analysis. The NO production of cells treated with RAPS (400 μg·mL-1) reached 15.8 μmol·L-L, which was 30.4-fold higher than that of the control (0.53 μmol·L-1). These data suggested that RAPS may enhance the immune function and protect against exogenous pathogens by activating macrophages. |
doi_str_mv | 10.3724/SP.J.1009.2016.00370 |
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In the present study, a polysaccharide component, Radix Adenophorae Polysaccharide (RAPS), was purified from Radix Adenophorae by decoloring with ADS-7 macroporous adsorption resin, DEAE-52 cellulose ion-exchange chromatography, and Sephacryl S-300HR gel chromatography, with the purity of 98.3% and a molecular weight of 1.8 × 104 Da. The cell viability assay and microscopic examination revealed that RAPS promoted the proliferation and activation of macrophages. At 400 μg·mL-1, RAPS stimulated RAW264.7 cell proliferation by 1.91-fold compared with the control. Meanwhile, RAPS significantly increased the secretion of pro-inflammatory cytokines (TNF-a and IL-6) in a dose-dependent manner in the supernatant of RAW264.7 cell culture as determined by ELISA. At 400 μg·mL-1, the production of TNF-a was 20.8-fold higher than that of the control. Simultaneously, the production of nitric oxide (NO) and the expression of inducible nitric oxide synthase (iNOS) were increased in RAW264.7 cells incubated with RAPS, as measured by Griess assay and Western blot analysis. The NO production of cells treated with RAPS (400 μg·mL-1) reached 15.8 μmol·L-L, which was 30.4-fold higher than that of the control (0.53 μmol·L-1). These data suggested that RAPS may enhance the immune function and protect against exogenous pathogens by activating macrophages.</description><identifier>ISSN: 2095-6975</identifier><identifier>ISSN: 1875-5364</identifier><identifier>EISSN: 1875-5364</identifier><identifier>DOI: 10.3724/SP.J.1009.2016.00370</identifier><identifier>PMID: 27478100</identifier><language>eng</language><publisher>China: Elsevier B.V</publisher><subject>Animals ; Campanulaceae - chemistry ; Cytokines - genetics ; Cytokines - immunology ; Immunologic Factors - pharmacology ; Interleukin-6 - genetics ; Interleukin-6 - immunology ; Macrophage activation ; Macrophage Activation - drug effects ; Macrophages - drug effects ; Macrophages - immunology ; Mice ; Nitric Oxide - immunology ; Plant Extracts - pharmacology ; Polysaccharide ; Polysaccharides - pharmacology ; Pro-inflammation ; Purification ; RAPS ; RAW264.7细胞 ; Tumor Necrosis Factor-alpha - genetics ; Tumor Necrosis Factor-alpha - immunology ; 多糖组分 ; 巨噬细胞 ; 沙参 ; 炎性细胞因子 ; 纯化 ; 细胞活化 ; 诱导型一氧化氮合酶</subject><ispartof>Chinese journal of natural medicines, 2016-05, Vol.14 (5), p.370-376</ispartof><rights>2016 China Pharmaceutical University</rights><rights>Copyright © 2016 China Pharmaceutical University. 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In the present study, a polysaccharide component, Radix Adenophorae Polysaccharide (RAPS), was purified from Radix Adenophorae by decoloring with ADS-7 macroporous adsorption resin, DEAE-52 cellulose ion-exchange chromatography, and Sephacryl S-300HR gel chromatography, with the purity of 98.3% and a molecular weight of 1.8 × 104 Da. The cell viability assay and microscopic examination revealed that RAPS promoted the proliferation and activation of macrophages. At 400 μg·mL-1, RAPS stimulated RAW264.7 cell proliferation by 1.91-fold compared with the control. Meanwhile, RAPS significantly increased the secretion of pro-inflammatory cytokines (TNF-a and IL-6) in a dose-dependent manner in the supernatant of RAW264.7 cell culture as determined by ELISA. At 400 μg·mL-1, the production of TNF-a was 20.8-fold higher than that of the control. Simultaneously, the production of nitric oxide (NO) and the expression of inducible nitric oxide synthase (iNOS) were increased in RAW264.7 cells incubated with RAPS, as measured by Griess assay and Western blot analysis. The NO production of cells treated with RAPS (400 μg·mL-1) reached 15.8 μmol·L-L, which was 30.4-fold higher than that of the control (0.53 μmol·L-1). These data suggested that RAPS may enhance the immune function and protect against exogenous pathogens by activating macrophages.</description><subject>Animals</subject><subject>Campanulaceae - chemistry</subject><subject>Cytokines - genetics</subject><subject>Cytokines - immunology</subject><subject>Immunologic Factors - pharmacology</subject><subject>Interleukin-6 - genetics</subject><subject>Interleukin-6 - immunology</subject><subject>Macrophage activation</subject><subject>Macrophage Activation - drug effects</subject><subject>Macrophages - drug effects</subject><subject>Macrophages - immunology</subject><subject>Mice</subject><subject>Nitric Oxide - immunology</subject><subject>Plant Extracts - pharmacology</subject><subject>Polysaccharide</subject><subject>Polysaccharides - pharmacology</subject><subject>Pro-inflammation</subject><subject>Purification</subject><subject>RAPS</subject><subject>RAW264.7细胞</subject><subject>Tumor Necrosis Factor-alpha - genetics</subject><subject>Tumor Necrosis Factor-alpha - immunology</subject><subject>多糖组分</subject><subject>巨噬细胞</subject><subject>沙参</subject><subject>炎性细胞因子</subject><subject>纯化</subject><subject>细胞活化</subject><subject>诱导型一氧化氮合酶</subject><issn>2095-6975</issn><issn>1875-5364</issn><issn>1875-5364</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9Udtq3DAQFaWlWdL8QSmiT32xK8uyLi-FJfQWAg1JSx_FWJJ3RdfSRrJD9zPyx5F3087LwJkz54x0EHrbkLoVlH28u6mv6oYQVVPS8JqQVpAXaNVI0VVdy9lLtKJEdRVXojtDFzn7ntC2lBDNa3RGBROyrK_Q4xrv4-6QwZgtJG8d3s_JD95ZPKQ44luw_i9eWxfifhsTlHmB4-QyNm63w2Am_wCTjwFDsMuw8mHYwTjCFNMBm8MU__hwXLOzORJ9wGMxKeDt-jflrBZ4BJOKAWxcfoNeDbDL7uK5n6NfXz7_vPxWXf_4-v1yfV2ZlrGpMpQPkhjGFO2YVb0UwoCyPS0otw0HAALWtNAZSoVUihvi-n4wrO8Yl117jj6cdMtl97PLkx59Xt4EwcU560YS2UouKS3Ud8_UuR-d1fvkR0gH_e8bC-HTieDKwQ_eJZ2Nd8E465Mzk7bR64boJTp9d6Ov9BKdXqLTx-iKwPuTgNnGsLn3YfPfhHOpJFdd1z4BHZSYlQ</recordid><startdate>20160501</startdate><enddate>20160501</enddate><creator>LI, Jing-Wen</creator><creator>LIU, Yang</creator><creator>LI, Bao-Hui</creator><creator>WANG, Yue-Yang</creator><creator>WANG, Hui</creator><creator>ZHOU, Chang-Lin</creator><general>Elsevier B.V</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20160501</creationdate><title>A polysaccharide purified from Radix Adenophorae promotes cell activation and pro-inflammatory cytokine production in murine RAW264.7 macrophages</title><author>LI, Jing-Wen ; LIU, Yang ; LI, Bao-Hui ; WANG, Yue-Yang ; WANG, Hui ; ZHOU, Chang-Lin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c344t-c26f80c449254d9b877ca9db2f806d16aaa0adc3a5c2278996c0ebbfc4b546853</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Campanulaceae - chemistry</topic><topic>Cytokines - genetics</topic><topic>Cytokines - immunology</topic><topic>Immunologic Factors - pharmacology</topic><topic>Interleukin-6 - genetics</topic><topic>Interleukin-6 - immunology</topic><topic>Macrophage activation</topic><topic>Macrophage Activation - drug effects</topic><topic>Macrophages - drug effects</topic><topic>Macrophages - immunology</topic><topic>Mice</topic><topic>Nitric Oxide - immunology</topic><topic>Plant Extracts - pharmacology</topic><topic>Polysaccharide</topic><topic>Polysaccharides - pharmacology</topic><topic>Pro-inflammation</topic><topic>Purification</topic><topic>RAPS</topic><topic>RAW264.7细胞</topic><topic>Tumor Necrosis Factor-alpha - genetics</topic><topic>Tumor Necrosis Factor-alpha - immunology</topic><topic>多糖组分</topic><topic>巨噬细胞</topic><topic>沙参</topic><topic>炎性细胞因子</topic><topic>纯化</topic><topic>细胞活化</topic><topic>诱导型一氧化氮合酶</topic><toplevel>online_resources</toplevel><creatorcontrib>LI, Jing-Wen</creatorcontrib><creatorcontrib>LIU, Yang</creatorcontrib><creatorcontrib>LI, Bao-Hui</creatorcontrib><creatorcontrib>WANG, Yue-Yang</creatorcontrib><creatorcontrib>WANG, Hui</creatorcontrib><creatorcontrib>ZHOU, Chang-Lin</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-医药卫生</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Chinese journal of natural medicines</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>LI, Jing-Wen</au><au>LIU, Yang</au><au>LI, Bao-Hui</au><au>WANG, Yue-Yang</au><au>WANG, Hui</au><au>ZHOU, Chang-Lin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A polysaccharide purified from Radix Adenophorae promotes cell activation and pro-inflammatory cytokine production in murine RAW264.7 macrophages</atitle><jtitle>Chinese journal of natural medicines</jtitle><addtitle>Chinese JOurnal of Natural Medicines</addtitle><date>2016-05-01</date><risdate>2016</risdate><volume>14</volume><issue>5</issue><spage>370</spage><epage>376</epage><pages>370-376</pages><issn>2095-6975</issn><issn>1875-5364</issn><eissn>1875-5364</eissn><abstract>Radix Adenophorae, a traditional Chinese medicine, has been reported to have a variety of biological functions. In the present study, a polysaccharide component, Radix Adenophorae Polysaccharide (RAPS), was purified from Radix Adenophorae by decoloring with ADS-7 macroporous adsorption resin, DEAE-52 cellulose ion-exchange chromatography, and Sephacryl S-300HR gel chromatography, with the purity of 98.3% and a molecular weight of 1.8 × 104 Da. The cell viability assay and microscopic examination revealed that RAPS promoted the proliferation and activation of macrophages. At 400 μg·mL-1, RAPS stimulated RAW264.7 cell proliferation by 1.91-fold compared with the control. Meanwhile, RAPS significantly increased the secretion of pro-inflammatory cytokines (TNF-a and IL-6) in a dose-dependent manner in the supernatant of RAW264.7 cell culture as determined by ELISA. At 400 μg·mL-1, the production of TNF-a was 20.8-fold higher than that of the control. Simultaneously, the production of nitric oxide (NO) and the expression of inducible nitric oxide synthase (iNOS) were increased in RAW264.7 cells incubated with RAPS, as measured by Griess assay and Western blot analysis. The NO production of cells treated with RAPS (400 μg·mL-1) reached 15.8 μmol·L-L, which was 30.4-fold higher than that of the control (0.53 μmol·L-1). These data suggested that RAPS may enhance the immune function and protect against exogenous pathogens by activating macrophages.</abstract><cop>China</cop><pub>Elsevier B.V</pub><pmid>27478100</pmid><doi>10.3724/SP.J.1009.2016.00370</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Campanulaceae - chemistry Cytokines - genetics Cytokines - immunology Immunologic Factors - pharmacology Interleukin-6 - genetics Interleukin-6 - immunology Macrophage activation Macrophage Activation - drug effects Macrophages - drug effects Macrophages - immunology Mice Nitric Oxide - immunology Plant Extracts - pharmacology Polysaccharide Polysaccharides - pharmacology Pro-inflammation Purification RAPS RAW264.7细胞 Tumor Necrosis Factor-alpha - genetics Tumor Necrosis Factor-alpha - immunology 多糖组分 巨噬细胞 沙参 炎性细胞因子 纯化 细胞活化 诱导型一氧化氮合酶 |
title | A polysaccharide purified from Radix Adenophorae promotes cell activation and pro-inflammatory cytokine production in murine RAW264.7 macrophages |
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