fth1在b ovis 019株侵染小鼠巨噬细胞中的功能研究-study on the function of ft h1 in murine macrophages infected by b ovis 019 strain.docx

fth1在b ovis 019株侵染小鼠巨噬细胞中的功能研究-study on the function of ft h1 in murine macrophages infected by b ovis 019 strain.docx

  1. 1、本文档共56页,可阅读全部内容。
  2. 2、原创力文档(book118)网站文档一经付费(服务费),不意味着购买了该文档的版权,仅供个人/单位学习、研究之用,不得用于商业用途,未经授权,严禁复制、发行、汇编、翻译或者网络传播等,侵权必究。
  3. 3、本站所有内容均由合作方或网友上传,本站不对文档的完整性、权威性及其观点立场正确性做任何保证或承诺!文档内容仅供研究参考,付费前请自行鉴别。如您付费,意味着您自己接受本站规则且自行承担风险,本站不退款、不进行额外附加服务;查看《如何避免下载的几个坑》。如果您已付费下载过本站文档,您可以点击 这里二次下载
  4. 4、如文档侵犯商业秘密、侵犯著作权、侵犯人身权等,请点击“版权申诉”(推荐),也可以打举报电话:400-050-0827(电话支持时间:9:00-18:30)。
查看更多
fth1在b ovis 019株侵染小鼠巨噬细胞中的功能研究-study on the function of ft h1 in murine macrophages infected by b ovis 019 strain

AbstractObject:BrucellosisisazoonticdiseasecausedbymembersofthegenusBrucella.Brucellamayparasiteinmacrophageandinhibitcellapoptosisatlong-term,whichcausesmany organsdamageandchronicinfectionforhumanandlivestock.Itisveryimportanttoexploretherelationbetweenbrucella’sintracellullarmechanismandchronicinfection.Theresultsofcurrentetiologicstudyshowthatoutermembraneproteins(OMPs)andtypeⅣsecretionsystem(TFSS)proteins areputative virulentfactorsbecausetheseelementsplayanimportantroleinbrucella’sinvasion,survivalandmultiplication.Thefunctionstudyofmacrophagetargetproteinsinteractingwithbrucellavirulentfactorsbecomesmolecularbasisofbrucella intracellullarparasitemechanism.Thisstudyisusefultoscreenspecificcandidatedrugstobrucellosis.Methods:(1)Toverificateferritinheavychain1(FTH1)interactedwithbrucellaTFSSVirB5 proteinbyco-immunoprecipitation(Co-IP).(2)ThetargetgenesincludingFTH1,16SrRNA, GAPDHandapoptosis-relatedgeneswerecloned,whoseStdandmeltcurveweremade.(3)ThreepositiveandonenegativepSIREN-siRNAstargetedtoFTH1weretransfectedintomouseRAW264.7macrophageswithTurboFectTMinvitroTransfectionReagent.TheoptimalpSIREN-siRNAwerescreenedbydetectingtheexpressionofFTH1byReal-timePCR. (4)TheoptimalpSIREN-siRNAwastransfectedintomouseRAW264.7macrophages.After48hthetransfectedmacrophageswereinfectedwithB.ovis019strain[0]for4handtheexpressionsof16SrRNAandapoptosis-relatedgeneswerequantitatedandcomparedby Real-timePCR.(5)Themorphologic change ofRAW264.7 macrophagesinfected withB.ovis 019strainbeforeRNAiandafterRNAiwereobservedbyelectronmicroscope.(6)ThecellculturefluidsupernatantofMouseRAW264.7macrophagestransfectedwithoptimalpSIREN-siRNAandinfectedwithB.ovis019strainfor15min,30min,1hand4hwasdetectedby ELISA.Results:(1)TheresultsofCo-IPshowedthatVirB5interactedwithFTH1.(2)TheeleventargetgenesincludingFTH1,16SrRNA,GAPDHandapoptosis-relatedgeneswereclonedandtheirStdvalueweremade.(3)ThreepositivesiRNAplasmidsweresuccessfullytransfectedintomouseRAW264.7macrophages.TheoptimalpSIREN-Cwasscreenedan

您可能关注的文档

文档评论(0)

peili2018 + 关注
实名认证
内容提供者

该用户很懒,什么也没介绍

1亿VIP精品文档

相关文档