简介:目的探索不同f2/f1比值对DPOAEs幅值的影响,寻找最佳的测试参数,以得到最大的DPOAEs测值.方法对12例(24耳)正常青年人进行不同f2/f1比值条件下的DPOAEs幅值测试.结果当f1/f1=1.220时,DPOAEs幅值最大(P<0.05或P<0.01).当f2/f1=1.232时,除了f2=2002Hz处以外,其DPOAEs幅值与f2/f1=1.220时无显著性差异(P>0.05).其他f2/f1值的DPOAEs幅值均较低,多数测值与f2/f1=1.220时相比均有显著性差异(P<0.05或P<0.01).结论f2/f1=1.220~1.232时,DPOAEs测值最大,此范围为最佳测试参数值.
简介:SincetheinventionofRubylaserbyMaimanin1960s,manykindsoflasersareusedwidelyindentistry.Ithasbeenprovedthatlaserirradiationcanproduceacidetchinglikesurface,thusstrengthenthebondofmaterialtoenamel.Buttheheatgeneratedduringirradiationproducesdamageondentalpulp,whichlimitsthelaserapplicationsondentalhardsurfaces.
简介:Objective:TodirectionallyclonetheomplgenefromChlamydiatrachomatis(Ct)FGenotypeontoaplasmidvectorforconstructingarudimentaryDNAvaccine.Methods:ThecompleteomplgenefromgenomicDNAofCtFgenotypewildspecieswasamplifiedwithprimersdesignedbycomputer.Therecombinantgenewasobtainedbyrestrictionenzymecutting,linkingthegenewiththeplasmidvectorinvitro,transformingtherecombinantgeneintobacteria,andextractingtheDNAfromthebacteria.Results:DNAextractingfromthebacteriawascomposedoftheimplgeneandplasmid,whichisidentifiedbythreemethodsofsingularrestrictiveenzymecutting,doublerestrictiveenzymecuttingandPCR.Conclusion:CloningoftheomplgenefromtheCtFgenotypemeansthatarudimentaryDNAvaccinewassuccessfullyconstructed.
简介:Thehousedustmites(Dermatophagoidesfarinae,Derf)arethemajorsourceofaeroallergensimplicatedintheexpressionofatopicdisorders,includingasthma,allergicrhinitisandatopicdermatitis.Inparticular,strongcircumstantialevidencesuggeststhathousedustmiteantigensareimportantprecipitatingfactorsofasthma.Manyhousedustmiteallergensareproteasesthatcanelicitairwayinflammationbystimulatingthereleaseofcytokinesfrombronchialepithelialcells.ToinvestigatewhetherDerfallergenproteasesinducedcytokineproductionfromtheepithelialcelllineBEAS-2B,BEAS-2Bcellswereculturedwith4differentconcentrationsofDerf(0.02,0.2,2,20μg/ml)for24-96h,afterwhichsupernatantswereassayedforinterleukin(IL)-6andIL-8withELISA.Reversetranscription-PCRwasalsoperformed.ThecellsheetswereintactthroughouttheobservationincontrolgroupwithoutanyexposuretoDerfantigen.IntheexperimentalgroupscellstreatedwithDerfallergenshowedchangesintheanchoragestatusofthemonolayer.Therewasasignificantincreaseinthelevelofcytokineproductioncomparedwiththeuntreatedsample.ThereleaseofIL-6andIL-8increasedinaconcentration-dependentmanner(P<0.05,respectively)withtheadditionofincreasingdosageofDerftothecellsheets.LevelsofIL-6andIL-8begantoriseat24hand48hafterallergenexposure,andtheyincreasedsignificantlyinthesupematantsat72hand96h.AtthesametimetheconcentrationdependenceofinductionofIL-6andIL-8expressionaswellasanincreaseintheexpressionofIL-6andIL-8mRNAmanifestedevidently.HDM-inducedairwayinflammationmayincludeDerf-mediatedreleaseofinflammatorymediators,andtheproteolyticactivityofanallergenmaystimulatethereleaseofproinflammatorycytokinesfromhumanbronchialepithelium.ItissuggestedthatIL-6andIL-8productionbybronchialepithelialcellsmayplayaroleinthepathogenesisofallergicasthma.
简介:Objective:ToinvestigatetheexpressionofE2FandBcl-2andtheclinicopathologicalsignificanceinhepatocellularcarcinoma.Methods:TheexpressionsofE2F-3andBcl-2in74patientswithhepaticcarcinoma,paracarcinomaand15patientswithlivercirrhosisweredetectedbyS-Pimmunohistochemicalstaining.Results:TheexpressionofE2Finhepaticcarcinomawassignificantlyhigherthanthatinparacarcinomaorlivercirrhosis(P<0.005),theexpressionofBcl-2inhepaticcarcinomawassignificantlyhigherthanthatinparacarcinoma(P<0.005),inwhichBcl-2expressionwaslowerthaninlivercirrhosis(P<0.05).TheexpressionofE2F-3wasrelatedwithhistologicalgrade,tumorsize,andtheexpressionofBcl-2wasrelatedwithhistologicalgrade,tumorsizeandtumornumber.TherewascorrelationbetweentheexpressionofE2F-3andBcl-2inhepaticcarcinoma.Conclusion:E2F-3andBcl-2expressionmayplayanimportantroleindevelopment,progressionandcellapoptosisoftumor.
简介:Objective:Tostudytheexpressionofactivatedepi-dermalgrowthfactorreceptor(EGFR)andtranscrip-tionfactorE2F(E2F)inCondylomaAccuminata(CA)patients.Methods:ImmunofluorescenttechniqueswereusedtoinvestigatetheexpressionofactivatedEGFRandE2FinCApatients.Results:TheexpressionofactivatedEGFRonthemembraneofepithelialcellsinCAlesionswassig-nificantlygreatercomparedtoexpressionleversinthecontrolgroup(P<0.01).Moreover,theco-expres-sionofactivatedEGFRandE2Fwassignificantlyin-creasedcomparedtothecontrolgroup(P<0.01).Conclusion:Ourobservationssuggestthatthein-creaseinactivatedEGFRexpressionmaystimulatehyperplasiainCApatientsthroughtheactivationoftranscriptionfactorE2F.
简介:Havingbeenpassedfor160generations,acelllinedesignatedasH22-F25/LwasestablishedfromamurinetumorlymphaticmetastatlcmodelH22-F25whichhadbeensetupinourcollege.Thecelllinewasinsuspensionculturewitharapidproliferationandstablegrowth.Thepeaktuneofcelldivisionandproliferationwas48and96hoursafterculture.Inaweek,thecellnumberwasIncreasedby25tunes.H22-F25/Lstillkeepsthefeaturesofapoorlydifferentiatedcancer.Itstumorinducingrate(invivo)was100%in615mice.Lymphnodemetastasisratewas50%andpulmonarymetastasisrate10%.H22-F25/LIsapopulationofheterogenetlctumorcellsIncluding2stemcelllines(themodelnumberofchromosomesbeing43in40%tumorcellsand86in32%)andsomesidelines.ThecommonmarkerchromosomesM1,M2,M3andM4werepresentinallstemandsidelines.
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简介:为了分析有免疫力的反应到老鼠的鼠科的hepatocarcinomaHca-F,与热吃惊使免疫(HSP70)蛋白质70源于elemene组合肿瘤Hca-F的房间疫苗(EC-TCV),HSP70被自动数据处理从EC-TCV孤立亲密关系层析。老鼠intraperitoneally与HSP70被使免疫三次,怒气房间被取样。为房间,他们对Hca-F的增长和cytotoxicity与MTT试金被测量,他们的显型与流动cytometry被分析。有HSP70的使免疫的鼠标的怒气房间比与EC-TCV使免疫的鼠标的比正常控制鼠标,而是更少的有势力的对Hca-F和增长展出了更多的有势力cytotoxicity。在三个组之中,在与HSP70(35.5%)使免疫的老鼠的T淋巴细胞的百分比在正常老鼠与6.25%相比是最高的,并且28.4%与EC-TCV在老鼠使免疫。从EC-TCV导出的HSP70的免疫能得到有势力免疫者反应到Hca-F。HSP70是对Hca-F导致反肿瘤免疫者回答的元素之一。细胞与分子的免疫学。2006;3(4):291-295。
简介:为研究乳宁Ⅱ号方(主药:生黄芪、太子参、当归、枸杞、天门冬、淫羊藿、鹿角片、米仁、莪术、八月札、露蜂房、山慈菇)的作用机理,将体外培养的MA891细胞接种在小鼠右腋皮下,然后将小鼠分为生理盐水组(A)、环磷酰胺(CTX)组(B)、CTX+乳宁Ⅱ号组(C)、乳宁Ⅱ号组(D)、扶正组(E)、祛邪组(F).各组小鼠分别给予相当于临床成人用量2倍的上述各种药物治疗.21天后处死小鼠,运用免疫组化和PT-PCR方法观察各组小鼠乳腺癌血管内皮生长因子(VEGF)及其受体f1K-1蛋白和mRNA的变化.结果:B、D、C、E、F组都能减少VEGF、f1K-1蛋白和mRNA的表达,其中C组效果最好,D组次之.提示:抑制VEGF、f1K-1的表达,从而抑制肿瘤的血管生成,可能是乳宁Ⅱ号的作用机理之一;乳宁Ⅱ号与化疗药CTX有协同作用.