简介:AIM:Toinvestigateandcomparethecytopathologicalandclinicaleffectsofamnioticmembranetransplantation(AMT)andoralmucosalmembranetransplantation(OMMT)insocketcontraction.METHODS:Twelvepatientswhocouldnotbefittedwithocularprosthesisduetosocketcontracturewereincludedinthisstudy.SevenpatientsunderwentAMTand5patientsunderwentOMMT.Thirteenpatientswhohadhealthysocketswereincludedascontrolgroup.Depthofinferiorfornix,degreeofinflammation,extentofthesocketcontractureandsocketvolumeweremeasuredinthepreoperativeperiodandatsixthandtwelfthweekspostoperatively.Impressioncytologyofconjunctivalfornicesandteartransforminggrowthfactorbeta-1(TGFβ1)levelsweredetermined.RESULTS:IntheAMTgroup,socketvolumeandlowerfornixdepthvaluesweresignificantlyhigher(P=0.030andP=0.004respectively)andinflammationlevelsandimpressioncytologystages(P=0.037andP=0.022respectively)weresignificantlylowerinpostoperativeperiodcomparedtopreoperativeperiod.IntheOMMTgroup,nostatisticaldifferenceswerefoundintermsofclinicalparameters,inflammationlevelsandimpressioncytologystagesofpreoperativeversuspostoperativevalues.PreoperativetearTGFβ1levelswerehigherinAMTandOMMTgroupscomparedtothecontrolgroup(25.5ng/mL,26.3ng/mLand21.7ng/mLrespectively).DecreasedtearTGFβ1levelswereobservedinboththeAMTandOMMTgroupspostoperatively(mediandecreasevalue=2.1ng/mLand2.7ng/mLrespectively).CONCLUSION:AMTisassociatedwithpostoperativeimprovementininferiorfornixdepth,socketvolume,inflammationandimpressioncytologylevelsandmaybeamoreproperalternativemethodthanOMMTinthemanagementofsocketcontracture.
简介:Traumaticinjuriestothecentralnervoussystem(CNS),includingtraumaticbraininjury(TBI)andspinalcordinjury(SCI),ofteninvolveanimmediatemechanicaldamagetoplasmamembranethatsurroundsneuronalsomataandaxons.Thisinitialdisruptionofplasmamembranefollowinginjurieshasbeenconvincinglydemonstratedbyincreasedmembrane
简介:对学习客观解剖并且cadaveric前臂的interosseous膜(马恩岛)的biomechanical特征。十radius-IOM-ulna结构从新鲜结冰死尸被收获测量马恩岛的腱的部分的长度,宽度和厚度的方法。然后,腱的部分与腱在测量以后属于的尺骨、光线的结束一起被孤立。半径的近似部分和尺骨的远侧的部分在牙齿的基础丙烯酸的树脂粉末被嵌入并且修理。嵌入的标本被MTS为全部张力的测试用10000N负担房间夹钳并且修理858测试机器。马恩岛以50mm/min的速度被拉长直到它被破裂。负担排水量曲线与一台计算机和最大的负担被描绘,僵硬同时被记录。结果前臂的马恩岛由三部分组成:中央腱的织物,膜的织物和背面的隶属于的倾斜的绳索。马恩岛在一个中立位置被拉长,并且在内转和旋后位置弯曲。当最大的负担的点到达了N到1021.50时,马恩岛的腱的部分在6个标本被撕碎吗?
简介:Rabbitlimbalcornealepithelialcells,cornealendothelialcellsandkeratocyteswereculturedonamnioticmembrane.Phasecontrastmicroscopeexaminationwasperformeddaily.Histologicalandscanelectronmicroscopicexaminationswerecarriedouttoobservethegrowth,arrangementandadhesionofcultivatedcells.Resultsshowedthatthreecornealcelltypesseededonamnioticmembranegrewwellandhadnormalcellmorphology.Culturedcellsattachedfirmlyonthesurfaceofamnioticmembrane.Cornealepithelialcellsshowedsingularlayerorstratification.Cellboundarieswereformedandtightlyopposed.Cornealendothelialcellsshowedcobblestoneorpolygonalmorphologiccharacteristicsthatappeareduniforminsize.Thecellulararrangementwascompact.Keratocyteselongatedandshowedtriangleordendriticmorphologywithmanyintercellularjointswhichcouldformnetworks.Inconclusion,amnioticmembranehasgoodscaffoldproperty,diffusioneffectandcompatibilitywithcornealcells.Thebasementmembranesideofamnioticmembranefacilitatedthegrowthofcornealepithelialcellsandendothelialcellsandcelljunctionsweretightlydeveloped.Thespongylayerofamnioticmembranefacilitatedthegrowthofkeratocytesandintercellularjointswererich.Amnioticmembraneisanidealbiomaterialforlayeringtissueengineeredcornea.
简介:DEVELOPMENTOFAVERSATILESENSINGMEMBRANEFORIMMUBILIZATIONOFPROTEINANDANEWIMMOBILIZATIONMETHODY.K.Zhou,J.W.Yuan,S.Q.Xu,B.H.Shu(D...
简介:Objective:Toconstructarecombinantplasmidcontainingtheoutermembraneprotein2(Omp2)geneofChlamydiatrachomatisandexpressOmp2inE.coli.Methods:Theomp2geneofC.trachomatisserovarDwasclonedintopQE30vectorfollowingPCRamplificationfromgenomicDNA.E.coliM15transformantswereinducedtoexpressthefusionproteinbyIPTGandtheproductwasidentifiedbySDS-PAGEandWesternblot.Results:ConfirmedbyenzymecleavageanalysisandDNAsequencing,acorrectrecombinantplasmidpQE30/omp2wasconstructed.Thefusionproteinfromthetransformantswasapproximately60kDainsizeinSDS-PAGEanalysis,whichcouldspeciallyreactwithanti-6×HismousemonoclonalIgGantibodies.Conclusion:WesuccessfullyexpressedOmp2inE.coilM15,providinganefficientandsimplesystemforassayingtheimmunologicalpropertiesofOmp2.
简介:Objectives:Recentstudieshaveintroducedmiddleearvolume(MEV)asanoveldeterminantofperforation-inducedconductivehearingloss(CHL)inamechanismdrivenbytrans-tympanicmembranepressuredifferences.Theprimaryaimsofthispreliminaryreportareto:1)correlateCHLwithperforationsize;2)describetherelationshipbetweenCHLandMEV;and3)compareCHLacrossarangeofcholesteatomainvolvement.Design:Aretrospectivepilotstudywasperformedin31subjectswithaudiometryindicativeofconductivehearingloss,temporalboneCTscans,andnopriormiddleearsurgery.PerforationsizeandMEVwereanalyzedwithrespecttoCHLinacohortof10perforatedearswithnocholesteatoma.CHLswerecomparedin3groupsdefinedbyextentofcholesteatomainvolvement.Results:EarswithlargeandsmallperforationsshowedmeanABGvaluesof32.0±15.7dBand16.0±16.4dB,respectively.AdirectrelationshipwasobservedbetweenMEVandCHLforearswithlargeperforationsacrossallfrequencies,whereasthisrelationshipforsmallperforationswasfrequency-dependent.Finally,astatisticallysignificantincreaseinCHLwasfoundacrossearswithincreasingcholesteatomainvolvementat1000Hz(c2(2)9.786,p0.008),2000Hz(c2(2)8.455,p0.015),and4000Hz(c2(2)8.253,p0.016).Conclusions:Thesepilotdatasuggestthatgreaterperforation-inducedconductivehearinglossesmaybeassociatedwithlargerperforationsizesandcholesteatoma.ThecorrelationbetweenMEVandCHLmayrequireadditionalstudy.
简介:Toobservetheprocessofinvasion,retinaofratwasusedasamodeltosubstitutetheinnerlimitingmembraneofretinaforthebasementmembrane.RetinainvadedbyesophagealcarcinomacellsandB16melanomacellsupontheinnerlimitingmembranewasstudiedbyscanningandtransmissionelectronmicroscopy.Theresultsshowedthattheinnerlimitingmembranewasdestroyedbybothkindsoftumorcells.Theprocessofdestructionwasfollowedbyaseriesoftransformationsintheinnerlimitingmembrane,i.e.folding,swelling,thickening,andgranularchange.Theinnerlimitingmembranewasdissolvedfocallyasaresultoftransformation,andthentumorcellsinvadedtheretinathroughthesedissolvedregions.Itseemsthat,asabarrier,theinnerlimitingmembraneplaysasimilarroleasthebasementmembrane.
简介:Tocloneandconstructtherecombinantplasmidcontainingthemajoroutermembraneprotein(MOMP)geneofChlamydiatrachomatis(C.trachomatis)andtoexpressthefusionproteininE.coliBL21,theMOMPgenewasamphfiedbypolymerasechainreaction(PCR)fromgenomeofC.trachomatisserovarD.ThefragmentwasclonedintotheprokaryoticexpressionvectorpET-22b(+)afterdigestionwithBamHⅠandNotⅠandtransformedintoE.coliXL1-Blue.RecombinantswereselectedbyenzymedigestionandsequencingandtherecombinantplasmidwithMOMPgenewasthentransformedintoE.coliBL21withIPTGtoexpressthetargetgene.TheexpressionrecombinantproteinswerepurifiedbyNi-NTAaffinitychromatography,andidentifiedbySDS-PAGEandWesternblot.Itwasfoundthata1.2kbMOMPgenewasisolated.TheDNAsequenceofMOMPwasfoundtobejustthesameasthesequencepublishedbyGenBank.ArecombinantplasmidcontainingMOMPgenewasconstructedtoexpressthefusionproteinsinE.coli.SDS-PAGEanalysisshowedthattherelativemolecularweightoftherecombinantproteinwasabout47kDathatwasconsistentwiththetheoreticalpredictedvalue,andthespecificityoftheexpressedproteinwasconformedbyWesternblot.ItconcludedthattheMOMPgenecouldbeexpressedintheprokaryoticsystem,bywhichitprovidedthefoundationforthefuturestudiesonthebiologicalactivitiesofC.trachomatisandforthedevelopmentofvaccineagainstthispathogen.
简介:Objective:Thepresentstudyaimedtoevaluatethepossibilityofusingcoherentanti-StokesRamanspectroscopy(CARS)microscopytodeterminethespecificmolecularmorphologyofcholesteatomabydetectingthenaturalvibrationalcontrastofthechemicalbondswithoutanystaining.Materialsandmethods:SpecimensfromthemastoidandtympanicmembranewithandwithoutcholesteatomawereanalyzedusingCARSmicroscopy,two-photonexcitedfluorescence(TPEF)microscopy,andthesecondharmonicgeneration(SHG)microscopy.Results:Incholesteatomatissuesfromthemastoid,astrongresonantsignalat2845cm-1wasobservedbyCARS,whichindicatedthedetectionoftheCH2hydro-carbonlipidbondsthatdonotgeneratevisiblesignalsat2940cm-1suggestiveofCH3bondsinaminoacids.Astrongresonantsignalat2940cm-1appearedinanareaofthesamespecimen,whichalsogeneratedabundantsignalsbyTPEFandSHGmicroscopyat817nm,whichwassuggestiveofcollagen.Inthetympanicmembranespecimenwithcholesteatoma,astrongresonantsignalwithcorrugatedmorphologywasdetected,whichindicatedthepresenceoflipids.AstrongsignalwasdetectedinthetympanicmembranewithchronicotitismediausingTPEF/SHGat817nm,whichindicatedcollagenenrichment.TheCARSandTPEF/SHGimageswereinaccordancewiththehistologyresults.Conclusion:TheseresultssuggesttheneedtodevelopanovelCARSmicroendoscopethatcanbeusedincombinationwithTPEF/SHGtodistinguishcholesteatomafrominflammatorytissues.
简介:AIMTo把主要、周期性的pterygium外科的长期的结果与三种不同技术作比较:联合结膜自体移植和覆盖羊膜的膜移植(有AMT的猫),结膜自体移植移植(猫)独自一个、羊膜的膜移植(AMT)alone.METHODSIn这回顾的研究,142个pterygium病人的142只眼睛(104主要,38周期性)经历了猫(组A),AMT(组B)或有AMT(组C)的猫分别地后面的外科的切除基于复发和手术后的complications.RESULTSThe数字被考察并且比较一样的描述在下面),18(10,8)并且2(1,1)在组A,B,和C分别地;干燥眼睛是22(16,6),27(18,9)并且7(3,4);结膜发炎是30(17,13),27(16,11)并且11(6,5)。在组C(主要或周期性的任何一个或两个)的病人主要在组A或B比那些显示出显著地更好的结果(P<0.05)关于上述临床的effects.CONCLUSIONCombined猫并且过分AMT比猫或AMT为主要、周期性的pterygium外科有复发和手术后的复杂并发症的显著地更低的率独自一个。
简介:ObjectiveTheaimofthisstudyistoinvestigatetheeffectoftransfectedhTERTgeneoncellapoptosisofnewbornratcochlearbasilarmembranecells(CBMCs).MethodsCBMCsisolatedfromnewbornratcochlearweretransfectedusingaplasmidcontaininghumantelomerasereverasetranscriptasegene(pCI-neo-hTERT),andwerescreenedusingG418toobtainstabletransfectedcelllines.Cellapoptosisratewasanalyzedbyflowcytometry.hTERTandapoptosisrelatedgenesexpressionweredetectedbyreversetranscriptasepolymerasechainreaction(RT-PCR).ResultshTERTgeneexpressionwasdetected72hoursaftergenetransfectionintransfectedcells.TheapoptoticrateoftransfectedCBMCssignificantlyreduced.Expressionofapoptosisrelatedgenescorrespondinglychanged.ConclusionTransfectionofhTERTgeneleadstoreducedapoptosisrateinnewbornratCBMCs.andlowerexpressionofapaf1,Caspase3andBCL2intransfectedcellsascomparedtothatofnormalCBMCs.
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简介:Objective:InfraredTympanicThermometer(ITT)isoneofthemostusefulinstrumentsforaccuratelymeasuringtemperature.TheeffectsofearpathologiesonITTmeasurementremainunclear.Thepurposeofthisstudyistodetermineiftympanicmembraneperforation(TMP)affectsITTmeasurementsinadultpatients.Materialandmethods:Atotalof90adultpatientswithmonauralcentralTMPwereenrolledinthisstudy.Patientswerecategorizedintothreesubgroupsaccordingtoperforationsize(1-3mm,4-7mm,and8-10mm).Thetympanictemperaturesoftheaffectedandunaffectedsites,andsubgroupswerecomparedwitheachother.Results:Thisstudycontained54(60%)malesand36(40%)femalesrangingfrom20to58yearsofage(meanage:30.74±9.61years).ThemeantympanictemperatureofthesideaffectedwithTMPwas36.34oC±0.61oC.Themeantympanictemperatureoftheunaffectedsidewithhealthyandintacttympanicmembranewas36.33oC±0.6oC.ThePearsoncorrelationscoreforthetympanictemperaturesandthesizeofTMPwas0.22whichwasnotsignificant(r=-0.12).Conclusion:TMPandperforationsizedonotaffectITTmeasurementsinadultpatients.
简介:EXPRESSIONOFEBVLATENTMEMBRANEPROTEININESOPHAGEALCARCINOMAANDPARACANCEROUSMUCOSAWuMingyao吴名耀LiangYingrui梁英锐WuXianying吴贤英Depar...
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简介:Theobjectiveofthispaperistodesignaporouspolyvinylalcohol(PVA)basedoncompositemembranewithcertainmechanicalstrengthandbiocompatibilitiesservingastissueregenerativescaffolds.PVA-glycosaminoglycan(GAG)-typeIcollagen(COL)compositemembranewasfabricatedbyPVAwithdifferentmolecularweight(Mw)andalcoholysisdegree(AD)beingblendedwithcertainamountsofGAGandCOLanddriedat38℃for24h.Thewatercontentofthecompositemembraneswerefrom61.9%to95.1%andswellingratiorangedfrom123.6%to621.7%.Scanningelectronmicroscope(SEM)analysisprovedthatPVA-GAG-COLcompositemembranehasporousandhomogenousstructure.Biocompatibilitytestresultsshowedthatthecompositemembranewasnontoxic,whichcouldpromoteadhesionandproliferationoffibroblastsonthecompositemembrane.Inconclusion,PVA-GAG-COLcompositemembranewithhighwatercontentandswellingratio,suitablemechanicalstrengthandgoodbiocompatibility,haspotentialintissueengineeringandregenerativemedicine.更多还原