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Rapamycin Modulates the Maturation of Rat Bone Marrow-derived Dendritic Cells
The purpose of the study was to observe the effect of rapamycin (RAPA) on the differentiation and maturation of rat bone marrow-derived dendritic cells (BMDCs) in vitro. BMDCs from Wistar rats were cultured with granulocyte-macrophage colony-stimulating factor plus interleukin-4 in the presence or a...
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Published in: | Journal of Huazhong University of Science and Technology. Medical sciences 2008-08, Vol.28 (4), p.391-395 |
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container_title | Journal of Huazhong University of Science and Technology. Medical sciences |
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creator | 丁英俊 程翔 唐婷婷 姚瑞 陈勇 谢江娇 余娴 廖玉华 |
description | The purpose of the study was to observe the effect of rapamycin (RAPA) on the differentiation and maturation of rat bone marrow-derived dendritic cells (BMDCs) in vitro. BMDCs from Wistar rats were cultured with granulocyte-macrophage colony-stimulating factor plus interleukin-4 in the presence or absence of RAPA (20 ng/mL), and stimulated with lipopolysaccharide (LPS) for 24 h before cells and supernatants were collected. Surface phenotype of BMDCs was flow-cytometrically detected to determine the expression of maturation markers, MHC class Ⅱ and CD86. Supernatants were analyzed for the production of IL-12 and IFN-γ cytokines by using ELISA. BMDCs were co-cultured with T cells from Lewis rats and mixed lymphocyte reaction was assessed by MTT method. The morphology of BMDCs stimulated with LPS remained immature after RAPA pretreatment. RAPA significantly decreased the CD86 expression, impaired the IL-12 and IFN-γ production of BMDCs stimulated with LPS, and inhibited the proliferation of allogeneic T cells. In conclusion, RAPA can inhibit the maturation of BMDCs stimulated with LPS in terms of the morphology, surface phenotype, cytokine production, and ability of BMDCs to stimulate the proliferation of allogeneic T cells in vitro. |
doi_str_mv | 10.1007/s11596-008-0405-1 |
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BMDCs from Wistar rats were cultured with granulocyte-macrophage colony-stimulating factor plus interleukin-4 in the presence or absence of RAPA (20 ng/mL), and stimulated with lipopolysaccharide (LPS) for 24 h before cells and supernatants were collected. Surface phenotype of BMDCs was flow-cytometrically detected to determine the expression of maturation markers, MHC class Ⅱ and CD86. Supernatants were analyzed for the production of IL-12 and IFN-γ cytokines by using ELISA. BMDCs were co-cultured with T cells from Lewis rats and mixed lymphocyte reaction was assessed by MTT method. The morphology of BMDCs stimulated with LPS remained immature after RAPA pretreatment. RAPA significantly decreased the CD86 expression, impaired the IL-12 and IFN-γ production of BMDCs stimulated with LPS, and inhibited the proliferation of allogeneic T cells. In conclusion, RAPA can inhibit the maturation of BMDCs stimulated with LPS in terms of the morphology, surface phenotype, cytokine production, and ability of BMDCs to stimulate the proliferation of allogeneic T cells in vitro.</description><identifier>ISSN: 1672-0733</identifier><identifier>EISSN: 1993-1352</identifier><identifier>DOI: 10.1007/s11596-008-0405-1</identifier><identifier>PMID: 18704298</identifier><language>eng</language><publisher>Heidelberg: Huazhong University of Science and Technology</publisher><subject>Animals ; BMDCs ; Bone Marrow Cells - cytology ; Cell Differentiation - drug effects ; Cell Differentiation - physiology ; Cells, Cultured ; Dendritic Cells - cytology ; Granulocyte-Macrophage Colony-Stimulating Factor - pharmacology ; Interleukin-4 - pharmacology ; Lipopolysaccharides - pharmacology ; Male ; Medicine ; Medicine & Public Health ; Rats ; Rats, Wistar ; Sirolimus - pharmacology ; 树突细胞 ; 脂多糖</subject><ispartof>Journal of Huazhong University of Science and Technology. Medical sciences, 2008-08, Vol.28 (4), p.391-395</ispartof><rights>Huazhong University of Science and Technology and Springer-Verlag GmbH 2008</rights><rights>Copyright © Wanfang Data Co. Ltd. All Rights Reserved.</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c358t-136f0d3b985b2a640656a625bb4f6e4d4fdd8b7cb448b9e1f57786249efa72ef3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/85740A/85740A.jpg</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18704298$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>丁英俊 程翔 唐婷婷 姚瑞 陈勇 谢江娇 余娴 廖玉华</creatorcontrib><title>Rapamycin Modulates the Maturation of Rat Bone Marrow-derived Dendritic Cells</title><title>Journal of Huazhong University of Science and Technology. Medical sciences</title><addtitle>J. Huazhong Univ. Sci. Technol. [Med. Sci.]</addtitle><addtitle>Journal of Zuazhong University of Science and Technology: Medical Edition</addtitle><description>The purpose of the study was to observe the effect of rapamycin (RAPA) on the differentiation and maturation of rat bone marrow-derived dendritic cells (BMDCs) in vitro. BMDCs from Wistar rats were cultured with granulocyte-macrophage colony-stimulating factor plus interleukin-4 in the presence or absence of RAPA (20 ng/mL), and stimulated with lipopolysaccharide (LPS) for 24 h before cells and supernatants were collected. Surface phenotype of BMDCs was flow-cytometrically detected to determine the expression of maturation markers, MHC class Ⅱ and CD86. Supernatants were analyzed for the production of IL-12 and IFN-γ cytokines by using ELISA. BMDCs were co-cultured with T cells from Lewis rats and mixed lymphocyte reaction was assessed by MTT method. The morphology of BMDCs stimulated with LPS remained immature after RAPA pretreatment. RAPA significantly decreased the CD86 expression, impaired the IL-12 and IFN-γ production of BMDCs stimulated with LPS, and inhibited the proliferation of allogeneic T cells. In conclusion, RAPA can inhibit the maturation of BMDCs stimulated with LPS in terms of the morphology, surface phenotype, cytokine production, and ability of BMDCs to stimulate the proliferation of allogeneic T cells in vitro.</description><subject>Animals</subject><subject>BMDCs</subject><subject>Bone Marrow Cells - cytology</subject><subject>Cell Differentiation - drug effects</subject><subject>Cell Differentiation - physiology</subject><subject>Cells, Cultured</subject><subject>Dendritic Cells - cytology</subject><subject>Granulocyte-Macrophage Colony-Stimulating Factor - pharmacology</subject><subject>Interleukin-4 - pharmacology</subject><subject>Lipopolysaccharides - pharmacology</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Sirolimus - pharmacology</subject><subject>树突细胞</subject><subject>脂多糖</subject><issn>1672-0733</issn><issn>1993-1352</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNp9kM1u1DAUhS0EoqXwAGxQxIZFFfC_kyUM5UfqCKmCtWXH19NMM_bUdmjn7fEoI3XHypb93XOPPoTeEvyRYKw-ZUJEL1uMuxZzLFryDJ2TvmctYYI-r3epaIsVY2foVc5bjIWSlL9EZ6RTmNO-O0frG7M3u8MwhmYd3TyZArkpt9CsTZmTKWMMTfTNjSnNlxiOzynFh9ZBGv-Ca75CcGks49CsYJrya_TCmynDm9N5gf58u_q9-tFe__r-c_X5uh2Y6EqtJz12zPadsNRIjqWQRlJhLfcSuOPeuc6qwXLe2R6IF0p1tXkP3igKnl2gyyX3wQRvwkZv45xC3ajL9nDnHh-tBlq1VCtYVPrDQu9TvJ8hF70b81D7mgBxzroKklJiSitJFnJIMecEXu_TuDPpoAnWR-V6Ua5rtj4q16TOvDulz3YH7mni5LgCdAFy_QobSE9t_5f6_tTkNobNfZ3T1gx3fpxA044x1mPC_gHFcZax</recordid><startdate>20080801</startdate><enddate>20080801</enddate><creator>丁英俊 程翔 唐婷婷 姚瑞 陈勇 谢江娇 余娴 廖玉华</creator><general>Huazhong University of Science and Technology</general><general>Institute of Cardiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022,China</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>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope></search><sort><creationdate>20080801</creationdate><title>Rapamycin Modulates the Maturation of Rat Bone Marrow-derived Dendritic Cells</title><author>丁英俊 程翔 唐婷婷 姚瑞 陈勇 谢江娇 余娴 廖玉华</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c358t-136f0d3b985b2a640656a625bb4f6e4d4fdd8b7cb448b9e1f57786249efa72ef3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>BMDCs</topic><topic>Bone Marrow Cells - cytology</topic><topic>Cell Differentiation - drug effects</topic><topic>Cell Differentiation - physiology</topic><topic>Cells, Cultured</topic><topic>Dendritic Cells - cytology</topic><topic>Granulocyte-Macrophage Colony-Stimulating Factor - pharmacology</topic><topic>Interleukin-4 - pharmacology</topic><topic>Lipopolysaccharides - pharmacology</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Sirolimus - pharmacology</topic><topic>树突细胞</topic><topic>脂多糖</topic><toplevel>online_resources</toplevel><creatorcontrib>丁英俊 程翔 唐婷婷 姚瑞 陈勇 谢江娇 余娴 廖玉华</creatorcontrib><collection>维普_期刊</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>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Wanfang Data Journals - Hong Kong</collection><collection>WANFANG Data Centre</collection><collection>Wanfang Data Journals</collection><collection>万方数据期刊 - 香港版</collection><collection>China Online Journals (COJ)</collection><collection>China Online Journals (COJ)</collection><jtitle>Journal of Huazhong University of Science and Technology. Medical sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>丁英俊 程翔 唐婷婷 姚瑞 陈勇 谢江娇 余娴 廖玉华</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rapamycin Modulates the Maturation of Rat Bone Marrow-derived Dendritic Cells</atitle><jtitle>Journal of Huazhong University of Science and Technology. Medical sciences</jtitle><stitle>J. Huazhong Univ. Sci. Technol. [Med. Sci.]</stitle><addtitle>Journal of Zuazhong University of Science and Technology: Medical Edition</addtitle><date>2008-08-01</date><risdate>2008</risdate><volume>28</volume><issue>4</issue><spage>391</spage><epage>395</epage><pages>391-395</pages><issn>1672-0733</issn><eissn>1993-1352</eissn><abstract>The purpose of the study was to observe the effect of rapamycin (RAPA) on the differentiation and maturation of rat bone marrow-derived dendritic cells (BMDCs) in vitro. BMDCs from Wistar rats were cultured with granulocyte-macrophage colony-stimulating factor plus interleukin-4 in the presence or absence of RAPA (20 ng/mL), and stimulated with lipopolysaccharide (LPS) for 24 h before cells and supernatants were collected. Surface phenotype of BMDCs was flow-cytometrically detected to determine the expression of maturation markers, MHC class Ⅱ and CD86. Supernatants were analyzed for the production of IL-12 and IFN-γ cytokines by using ELISA. BMDCs were co-cultured with T cells from Lewis rats and mixed lymphocyte reaction was assessed by MTT method. The morphology of BMDCs stimulated with LPS remained immature after RAPA pretreatment. RAPA significantly decreased the CD86 expression, impaired the IL-12 and IFN-γ production of BMDCs stimulated with LPS, and inhibited the proliferation of allogeneic T cells. 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subjects | Animals BMDCs Bone Marrow Cells - cytology Cell Differentiation - drug effects Cell Differentiation - physiology Cells, Cultured Dendritic Cells - cytology Granulocyte-Macrophage Colony-Stimulating Factor - pharmacology Interleukin-4 - pharmacology Lipopolysaccharides - pharmacology Male Medicine Medicine & Public Health Rats Rats, Wistar Sirolimus - pharmacology 树突细胞 脂多糖 |
title | Rapamycin Modulates the Maturation of Rat Bone Marrow-derived Dendritic Cells |
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