Macrophage Cell Lines Derived from Major Histocompatibility Complex Ii-Negative Mice
Two bone-marrow-derived macrophage cell lines, C2D and C2Dt, were isolated from major histocompatibility class II-negative knock-out mice. The C2D cell line was stabilized by continuous culture in colony-stimulating factor-1 and the C2Dt cell line was transformed with SV40 virus large T antigen. The...
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Veröffentlicht in: | In vitro cellular & developmental biology. Animal 1998-06, Vol.34 (6), p.499-507 |
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description | Two bone-marrow-derived macrophage cell lines, C2D and C2Dt, were isolated from major histocompatibility class II-negative knock-out mice. The C2D cell line was stabilized by continuous culture in colony-stimulating factor-1 and the C2Dt cell line was transformed with SV40 virus large T antigen. These cells exhibited phenotypic properties of macrophages including morphology and expression of Mac 1 and Mac 2 cell surface molecules. These cells also had comparable growth to the bone-marrow-derived macrophage cell line B6MP102. These new cell lines were not spontaneously cytotoxic and were only capable of modest killing of F5b tumor cells when stimulated with LPS and interferon-y, but not when stimulated with LPS alone or with staphylococcal exotoxin. C2D and C2Dt cells phagocytosed labeled Staphylococcus aureus similarly to B6MP102 cells but less well than C2D peritoneal macrophages. These cell lines secreted interleukin-6, but not tumor necrosis factor or nitric oxide in response to LPS or staphylococcal enterotoxins A or B. C2Dt cells were tumorigenic in C2D and C57BL/6J mice but C2D cells were not. These data suggest that macrophage cell lines can be established from bone marrow cells of major histocompatibility complex II-negative mice. |
doi_str_mv | 10.1007/s11626-998-0085-y |
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The C2D cell line was stabilized by continuous culture in colony-stimulating factor-1 and the C2Dt cell line was transformed with SV40 virus large T antigen. These cells exhibited phenotypic properties of macrophages including morphology and expression of Mac 1 and Mac 2 cell surface molecules. These cells also had comparable growth to the bone-marrow-derived macrophage cell line B6MP102. These new cell lines were not spontaneously cytotoxic and were only capable of modest killing of F5b tumor cells when stimulated with LPS and interferon-y, but not when stimulated with LPS alone or with staphylococcal exotoxin. C2D and C2Dt cells phagocytosed labeled Staphylococcus aureus similarly to B6MP102 cells but less well than C2D peritoneal macrophages. These cell lines secreted interleukin-6, but not tumor necrosis factor or nitric oxide in response to LPS or staphylococcal enterotoxins A or B. C2Dt cells were tumorigenic in C2D and C57BL/6J mice but C2D cells were not. These data suggest that macrophage cell lines can be established from bone marrow cells of major histocompatibility complex II-negative mice.</description><identifier>ISSN: 1071-2690</identifier><identifier>EISSN: 1543-706X</identifier><identifier>DOI: 10.1007/s11626-998-0085-y</identifier><identifier>PMID: 9661055</identifier><identifier>CODEN: IVCAED</identifier><language>eng</language><publisher>Legacy CDMS: Society for In Vitro Biology</publisher><subject>3T3 cells ; Animals ; Antigen T (large) ; Antigens ; Bone growth ; Bone marrow ; Bone marrow cells ; Carcinogenicity Tests ; Cell culture ; Cell Line ; Cell Line, Transformed ; Cell lines ; Cell surface ; Colony-stimulating factor ; Continuous culture ; Cultured cells ; Cytokines - secretion ; Cytology ; Cytotoxicity ; Exotoxins ; Histocompatibility Antigens Class II - physiology ; Immunology ; Interferon ; Interleukin 6 ; Interleukins ; Life Sciences (General) ; Lipopolysaccharides ; Macrophage colony-stimulating factor ; Macrophages ; Macrophages - cytology ; Macrophages - metabolism ; Macrophages - physiology ; Major histocompatibility complex ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Molecules ; Nitric oxide ; Phagocytosis ; Phenotype ; Superantigens - metabolism ; Transformed cell line ; Tumor cell line ; Tumor cells ; Tumors ; Viruses ; γ-Interferon</subject><ispartof>In vitro cellular & developmental biology. Animal, 1998-06, Vol.34 (6), p.499-507</ispartof><rights>Copyright 1998 Society for In Vitro Biology</rights><rights>Copyright Society for In Vitro Biology Jun 1998</rights><rights>Society for In Vitro Biology 1998.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c424t-e950957deb57016ab8064680659db4f5ca544d3394beb5d6ce8b1adda9e8f55c3</citedby><cites>FETCH-LOGICAL-c424t-e950957deb57016ab8064680659db4f5ca544d3394beb5d6ce8b1adda9e8f55c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/4294805$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/4294805$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,803,27924,27925,58017,58250</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9661055$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Beharka, Alison A.</creatorcontrib><creatorcontrib>Armstrong, Jason W.</creatorcontrib><creatorcontrib>Chapes, Stephen K.</creatorcontrib><title>Macrophage Cell Lines Derived from Major Histocompatibility Complex Ii-Negative Mice</title><title>In vitro cellular & developmental biology. Animal</title><addtitle>In Vitro Cell Dev Biol Anim</addtitle><description>Two bone-marrow-derived macrophage cell lines, C2D and C2Dt, were isolated from major histocompatibility class II-negative knock-out mice. The C2D cell line was stabilized by continuous culture in colony-stimulating factor-1 and the C2Dt cell line was transformed with SV40 virus large T antigen. These cells exhibited phenotypic properties of macrophages including morphology and expression of Mac 1 and Mac 2 cell surface molecules. These cells also had comparable growth to the bone-marrow-derived macrophage cell line B6MP102. These new cell lines were not spontaneously cytotoxic and were only capable of modest killing of F5b tumor cells when stimulated with LPS and interferon-y, but not when stimulated with LPS alone or with staphylococcal exotoxin. C2D and C2Dt cells phagocytosed labeled Staphylococcus aureus similarly to B6MP102 cells but less well than C2D peritoneal macrophages. These cell lines secreted interleukin-6, but not tumor necrosis factor or nitric oxide in response to LPS or staphylococcal enterotoxins A or B. C2Dt cells were tumorigenic in C2D and C57BL/6J mice but C2D cells were not. These data suggest that macrophage cell lines can be established from bone marrow cells of major histocompatibility complex II-negative mice.</description><subject>3T3 cells</subject><subject>Animals</subject><subject>Antigen T (large)</subject><subject>Antigens</subject><subject>Bone growth</subject><subject>Bone marrow</subject><subject>Bone marrow cells</subject><subject>Carcinogenicity Tests</subject><subject>Cell culture</subject><subject>Cell Line</subject><subject>Cell Line, Transformed</subject><subject>Cell lines</subject><subject>Cell surface</subject><subject>Colony-stimulating factor</subject><subject>Continuous culture</subject><subject>Cultured cells</subject><subject>Cytokines - secretion</subject><subject>Cytology</subject><subject>Cytotoxicity</subject><subject>Exotoxins</subject><subject>Histocompatibility Antigens Class II - physiology</subject><subject>Immunology</subject><subject>Interferon</subject><subject>Interleukin 6</subject><subject>Interleukins</subject><subject>Life Sciences (General)</subject><subject>Lipopolysaccharides</subject><subject>Macrophage colony-stimulating factor</subject><subject>Macrophages</subject><subject>Macrophages - cytology</subject><subject>Macrophages - metabolism</subject><subject>Macrophages - physiology</subject><subject>Major histocompatibility complex</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>Molecules</subject><subject>Nitric oxide</subject><subject>Phagocytosis</subject><subject>Phenotype</subject><subject>Superantigens - metabolism</subject><subject>Transformed cell line</subject><subject>Tumor cell line</subject><subject>Tumor cells</subject><subject>Tumors</subject><subject>Viruses</subject><subject>γ-Interferon</subject><issn>1071-2690</issn><issn>1543-706X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>CYI</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp1kVmLFDEUhYMo4zj6AwSFoOBb9KayVPI4tMsMdOvLCL6FVNWtMU0tbVI92P_eO3QzgmAest3vnCyHsZcS3kuA-kOR0lZWeO8EgDPi8IidS6OVqMH-eExzqKWorIen7FkpW6DmpT1jZ95aCcacs5tNbPO8-xlvka9wGPg6TVj4R8zpDjve53nkm7idM79KZZnbedzFJTVpSMuBr2g14G9-ncRXvKX9O-Sb1OJz9qSPQ8EXp_GCff_86WZ1JdbfvlyvLtei1ZVeBHoD3tQdNqYGaWPjwGpLnfFdo3vTRqN1p5TXDSGdbdE1MnZd9Oh6Y1p1wd4dfXd5_rXHsoQxlZZeESec9yVIa0CRH4Fv_wG38z5PdLdQWauddt4rot78l1La-1qCI0geIfq2UjL2YZfTGPMhSAj3oYRjKIFCCfehhANpXp-M982I3YPilALVXx3rUywxTEumAwE0yLqyyv4tbymB_KDWldcOjPoDD6iYZQ</recordid><startdate>19980601</startdate><enddate>19980601</enddate><creator>Beharka, Alison A.</creator><creator>Armstrong, Jason W.</creator><creator>Chapes, Stephen K.</creator><general>Society for In Vitro Biology</general><scope>CYE</scope><scope>CYI</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>3V.</scope><scope>4T-</scope><scope>7QL</scope><scope>7T7</scope><scope>7TK</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>S0X</scope><scope>7QO</scope></search><sort><creationdate>19980601</creationdate><title>Macrophage Cell Lines Derived from Major Histocompatibility Complex Ii-Negative Mice</title><author>Beharka, Alison A. ; Armstrong, Jason W. ; Chapes, Stephen K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c424t-e950957deb57016ab8064680659db4f5ca544d3394beb5d6ce8b1adda9e8f55c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>3T3 cells</topic><topic>Animals</topic><topic>Antigen T (large)</topic><topic>Antigens</topic><topic>Bone growth</topic><topic>Bone marrow</topic><topic>Bone marrow cells</topic><topic>Carcinogenicity Tests</topic><topic>Cell culture</topic><topic>Cell Line</topic><topic>Cell Line, Transformed</topic><topic>Cell lines</topic><topic>Cell surface</topic><topic>Colony-stimulating factor</topic><topic>Continuous culture</topic><topic>Cultured cells</topic><topic>Cytokines - secretion</topic><topic>Cytology</topic><topic>Cytotoxicity</topic><topic>Exotoxins</topic><topic>Histocompatibility Antigens Class II - physiology</topic><topic>Immunology</topic><topic>Interferon</topic><topic>Interleukin 6</topic><topic>Interleukins</topic><topic>Life Sciences (General)</topic><topic>Lipopolysaccharides</topic><topic>Macrophage colony-stimulating factor</topic><topic>Macrophages</topic><topic>Macrophages - cytology</topic><topic>Macrophages - metabolism</topic><topic>Macrophages - physiology</topic><topic>Major histocompatibility complex</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>Molecules</topic><topic>Nitric oxide</topic><topic>Phagocytosis</topic><topic>Phenotype</topic><topic>Superantigens - metabolism</topic><topic>Transformed cell line</topic><topic>Tumor cell line</topic><topic>Tumor cells</topic><topic>Tumors</topic><topic>Viruses</topic><topic>γ-Interferon</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Beharka, Alison A.</creatorcontrib><creatorcontrib>Armstrong, Jason W.</creatorcontrib><creatorcontrib>Chapes, Stephen K.</creatorcontrib><collection>NASA Scientific and Technical Information</collection><collection>NASA Technical Reports Server</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>Biotechnology Research Abstracts</collection><jtitle>In vitro cellular & developmental biology. Animal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Beharka, Alison A.</au><au>Armstrong, Jason W.</au><au>Chapes, Stephen K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Macrophage Cell Lines Derived from Major Histocompatibility Complex Ii-Negative Mice</atitle><jtitle>In vitro cellular & developmental biology. Animal</jtitle><addtitle>In Vitro Cell Dev Biol Anim</addtitle><date>1998-06-01</date><risdate>1998</risdate><volume>34</volume><issue>6</issue><spage>499</spage><epage>507</epage><pages>499-507</pages><issn>1071-2690</issn><eissn>1543-706X</eissn><coden>IVCAED</coden><abstract>Two bone-marrow-derived macrophage cell lines, C2D and C2Dt, were isolated from major histocompatibility class II-negative knock-out mice. The C2D cell line was stabilized by continuous culture in colony-stimulating factor-1 and the C2Dt cell line was transformed with SV40 virus large T antigen. These cells exhibited phenotypic properties of macrophages including morphology and expression of Mac 1 and Mac 2 cell surface molecules. These cells also had comparable growth to the bone-marrow-derived macrophage cell line B6MP102. These new cell lines were not spontaneously cytotoxic and were only capable of modest killing of F5b tumor cells when stimulated with LPS and interferon-y, but not when stimulated with LPS alone or with staphylococcal exotoxin. C2D and C2Dt cells phagocytosed labeled Staphylococcus aureus similarly to B6MP102 cells but less well than C2D peritoneal macrophages. These cell lines secreted interleukin-6, but not tumor necrosis factor or nitric oxide in response to LPS or staphylococcal enterotoxins A or B. C2Dt cells were tumorigenic in C2D and C57BL/6J mice but C2D cells were not. These data suggest that macrophage cell lines can be established from bone marrow cells of major histocompatibility complex II-negative mice.</abstract><cop>Legacy CDMS</cop><pub>Society for In Vitro Biology</pub><pmid>9661055</pmid><doi>10.1007/s11626-998-0085-y</doi><tpages>9</tpages></addata></record> |
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subjects | 3T3 cells Animals Antigen T (large) Antigens Bone growth Bone marrow Bone marrow cells Carcinogenicity Tests Cell culture Cell Line Cell Line, Transformed Cell lines Cell surface Colony-stimulating factor Continuous culture Cultured cells Cytokines - secretion Cytology Cytotoxicity Exotoxins Histocompatibility Antigens Class II - physiology Immunology Interferon Interleukin 6 Interleukins Life Sciences (General) Lipopolysaccharides Macrophage colony-stimulating factor Macrophages Macrophages - cytology Macrophages - metabolism Macrophages - physiology Major histocompatibility complex Mice Mice, Inbred C57BL Mice, Knockout Molecules Nitric oxide Phagocytosis Phenotype Superantigens - metabolism Transformed cell line Tumor cell line Tumor cells Tumors Viruses γ-Interferon |
title | Macrophage Cell Lines Derived from Major Histocompatibility Complex Ii-Negative Mice |
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