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简介：Multipleregenerationofaxonalbudshasbeenshowntoexistduringtherepairofperipheralnerveinjury,whichconfirmsacertainrepairpotentialoftheinjuredperipheralnerve.Therefore,asystematicnervetranspositionrepairtechniquehasbeenproposedtotreatsevereperipheralnerveinjury.Duringnervetranspositionrepair,theregeneratednervefibersofmotorneuronsintheanteriorhornofthespinalcordcaneffectivelygrowintotherepaireddistalnerveandtargetmuscletissues,whichisconducivetotherecoveryofmotorfunction.Theaimofthisstudywastoexploreregenerationandnervefunctionalrecoveryafterrepairingalong-segmentperipheralnervedefectbytranspositionofdifferentdonornerves.Along-segment(2mm)ulnarnervedefectinSprague-Dawleyratswasrepairedbytranspositionofthemusculocutaneousnerve,medialpectoralnerve,muscularbranchesoftheradialnerveandanteriorinterosseousnerve(pronatorquadratusmusclebranch).Insiturepairoftheulnarnervewasconsideredasacontrol.Threemonthslater,wristflexionfunction,nerveregenerationandinnervationmusclerecoveryinratswereassessedusingneuroelectrophysiologicaltesting,osmicacidstainingandhematoxylin-eosinstaining,respectively.Ourfindingsindicatethatrepairofalong-segmentulnarnervedefectwithdifferentdonornervetranspositionscanreinnervateaxonalfunctionofmotorneuronsintheanteriorhornofspinalcordandrestorethefunctionofaffectedlimbstoacertainextent.

简介：AbstractBackground:Hyperbaric oxygen treatment (HBOT) has been demonstrated to influence the keloid recurrence rate after surgery and to relieve keloid symptoms and other pathological processes in keloids. To explore the mechanism of the effect of HBOT on keloids, tumor immune gene expression and immune cell infiltration were studied in this work.Methods:From February 2021 to April 2021, HBOT was carried out on keloid patients four times before surgery. Keloid tissue samples were collected and divided into an HBOT group (keloid with HBOT before surgery [HK] group, n = 6) and a non-HBOT group (K group, n = 6). Tumor gene expression was analyzed with an Oncomine Immune Response Research Assay kit. Data were mined with R package. The differentially expressed genes between the groups were compared. Hub genes between the groups were determined and verified with Quantitative Real-time PCR. Immune cell infiltration was analyzed based on CIBERSORT deconvolution algorithm analysis of gene expression and verified with immunohistochemistry (IHC).Results:Inflammatory cell infiltration was reduced in the HK group. There were 178 upregulated genes and 217 downregulated genes. Ten hub genes were identified, including Integrin Subunit Alpha M (ITGAM), interleukin (IL)-4, IL-6, IL-2, Protein Tyrosine Phosphatase Receptor Type C (PTPRC), CD86, transforming growth factor (TGF), CD80, CTLA4, and IL-10. CD80, ITGAM, IL-4, and PTPRC with significantly downregulated expression were identified. IL-10 and IL-2 were upregulated in the HK group but without a significant difference. Infiltration differences of CD8 lymphocyte T cells, CD4 lymphocyte T-activated memory cells, and dendritic resting cells were identified with gene CIBERSORT deconvolution algorithm analysis. Infiltration levels of CD4 lymphocyte T cell in the HK group were significantly higher than those of the K group in IHC verification.Conclusion:HBOT affected tumor gene expression and immune cell infiltration in keloids. CD4 lymphocyte T cell, especially activated memory CD4+T, might be the key regulatory immune cell, and its related gene expression needs further study.

简介：ＳＴＵＤＹＯＮＭＥＴＡＳＴＡＳＩＳＡＳＳＯＣＩＡＴＥＤＧＥＮＥＳＣＲＥＥＮＥＤＢＹＭＯＮＯＣＬＯＮＡＬＡＮＴＩＢＯＤＹＨＩＬＱｉＴｅｎｇｐｉｎｇ齐藤平；Ｚｈａｎｇｐｅｉｊｉ张沛基；ＷｅｉＳｈｕｇｕａｎｇ魏曙光；ＣｈｅｎＤｏｎｇ陈东；ＬｉＲｅｎ李仁；Ｗ...

简介：Object:ToidentifytranscriptvariantsandexpressionpatternsofporcineMitf.Materialsandmethods:ApairwiseBLASTsearchatNCBIdatabasewasperformedtodeducethestructureofporcineMitfgene.Subsequently,50RACEandfluorescentquantitativeRT-PCRwereusedtoanalyzetheexpressionpatternofporcineMitfindifferenttissues.Results:FourtranscriptvariantsofporcineMitf,MITF-A,MITF-H,MITF-MandMITF-SUSwereidentified,allsharinghighhomologywiththoseinhumans,exceptMitf-SUS.Conclusion:ThesequenceofporcineMitfappearhighlyhomologoustohumanMITF.However,only4transcriptvariantsofporcineMitfwereidentifiedintheseminipigs,lessthanthe9transcriptvariantsinhumanMITF.

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简介：WeclonedcDNAsforXenopusaldolasesA,BandC.Thesethreealdolasegenesarelocalizedondifferentchromosomesasasinglecopygene.Intheadult,thealdolaseAgeneisexpressedextensivelyinmuscletissues,whereasthealdolaseBgeneisexpressedstronglyinkidney,liver,stomachandintestine,whilethealdolaseCgeneisexpressedinbrain,heartandovary.InoocytesaldolaseAandCmRNAs,butnotaldolaseBmRNA,areextensivelytranscribed.Thus,aldolaseAandCmRNAs,butnotBmRNA,occurabundantlyineggsasmaternalmRNAs,andstrongexpressionofaldolaseBmRNAisseenonlyafterthelateneurulastage.WeconcludethataldolaseAandCmRNAsaremajoraldolasemRNAsinearlystagesofXenopusembryogenesiswhichproceedsutilizingyolkastheonlyenergysource,aldolaseBmRNA,ontheotherhand,isexpressedonlylaterindevelopmentintissueswhicharerequiredfordietaryfructosemetabolism.WealsoisolatedtheXenopusaldolaseCgenomicgene(ca.12kb)andfoundthatitspromoter(ca.2kb)containsregionsnecessaryfortissue-specificexpressionandalsoaGCrichregionwhichisessentialforbasaltranscriptionalactivity.

简介：Cowdensyndrome(CS),anautosomaldominantdisorder,isoneofaspectrumofclinicaldisordersthathavebeenlinkedtogermlinemutationsinthephosphataseandtensinhomolog(PTEN)gene.Although70-80%ofpatientswithCShaveanidentifiablegermlinePTENmutation,theclinicaldiagnosispresentsmanychallengesbecauseofthephenotypicandgenotypicvariations.Inthepresentstudy,wesequencedtheexonsandthepromoterofPTENgene,mutationsandvariationsinthepromoterandexonswereidentified,andaPTENproteinexpressionnegativeregionwasdeterminedbyimmunohistochemistry(IHC).Inconclusion,anovelpromotermutationwefoundinPTENgenemayturnoffPTENproteinexpressionoccasionally,leadingtothedisorderofPTENanduntypicalCSmanifestations.

简介：AbstractObjective:To investigate the effects of vitrification on the expression of the imprinted gene Snrpn in neonatal placental tissue.Methods:Neonatal placental tissue was collected from women with natural pregnancy (control group) and from women in assisted reproductive technology (ART) pregnancy group, following fresh and vitrified embryo transfer (fresh group and vitrified group, respectively). Snrpn mRNA expression and SNRPN protein levels in placental tissue from these three groups were assessed by real-time reverse transcription polymerase chain reaction and Western blot, respectively. DNA methylation in the Snrpn promoter region was analyzed by bisulfite-pyrosequencing.Results:The expression of Snrpn mRNA and SNRPN protein was found to be higher in placental tissue from the fresh and vitrified ART groups, compared to the control group. There was no significant difference in SNRPN gene or protein expression between the fresh and vitrified groups. DNA methylation at the Snrpn promoter region was not significantly different between these three groups.Conclusions:Human ART may alter the transcriptional expression and protein levels of the imprinted gene Snrpn. However, compared to other ART methods, vitrification may not aggravate or reduce this effect. Moreover, the altered expression of Snrpn is likely not directly related to DNA methylation of the Snrpn promoter region.

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简介：43个米饭变化的DNA碎片被放大，11份教材基于植物的抵抗基因类似物(RGA)设计了，并且变化的强风抵抗被接种与33识别从云南省收集的Magnaporthegrisea孤立，中国。聚类结果与0.6117的一个关联系数揭示了在强风抵抗和DNA乐队之间的重要关联(α=0.01)，显示抵抗分析基于接种与那基于聚类分析的RGA-PCR与一致。关联系数，然而，从0.1701～0.535取决于教材。五份教材，S1/AS3，S1INV/S2INV，XLRRFor/XLRR加快，Pto-Kin1IN/Pto-Kin2在，和NLRRFor/NLRR加快可能被申请在他们的乐队数字和多型性的考虑的强风抵抗鉴定，和他们有强风抵抗的关联系数是0.5305，0.4898，0.4059，0.3719和0.3524分别地。而且，除了二个高度易受影响的变化，CO39和Lijiangxintuanheigu的indica和装饰用的梨树米饭，能被11份教材很好分类。

简介：Objective:Toinvestigatetherelationshipbetweengenemutationandpathologicaltypeoflungcancer,inspectandverifytheconsistencybetweenhomologousgenesmutationinvariouspathologictype.Methods:CombinedwiththeCOSMICandUniProtdatabase,weobtainedthereportedoverallbig-samplemutationdataoflungcancerandtheproteinsequencesofthetop20mutatedgenes,respectively.Analyzethedataandclustertheproteinsequencesandthendeducethehomologousgene.Ultimately,analyzethemutationsofdifferentpathologicaltypesofhomologousgenes.Results:TP53(32.32%)hasthehighestmutationrateinlungcancer,followedbyEGFR(29.12%).Thecopynumbervariability(CNV)ofgenes:KRAS,LRP1B,CDKN2A,KMT2C,FAT1,PIK3CA,RB1,ERBB4,GRIN2AandKDRbetweeneachpathologicaltypeisstaticallysignificant(P<0.05).ThegenedifferentialexpressionratebetweenadenocarcinomaandsquamouscarcinomaofgeneTP53,KRAS,LRP1B,CDKN2A,STK11,FAT4,KMT2D,NFE2L2,KEAP1,PIK3CA,RB1,ERBB4,SMARCA4andKDRarestatisticallysignificant(P<0.05).ThesimilarityoftheproteinsequenceofEGFRandERBB4canreach93%,andFAT4andFAT1are81%.Forsmallcellcarcinoma,there’snodifferenceinCNVbetweenthetwogroupsofhomologousgenes,andnodifferencebetweenFAT4andFAT1inadenocarcinoma.Conclusion:TheCNVandgeneexpressionoflungcancer-associatedgenesarerelevanttopathologictypes.GFRandERBB4arehomologous,FAT4andFAT1arealsoamongthetop20mutationgenes.Additionally,there’snodifferenceinCNVbetweenthetwogroupsofsmallcellcarcinoma,whichisthesamebetweenFAT4andFAT1inadenocarcinoma.

简介：Objective:Tounderstandthecrucialroleoftheklothogeneinhearingdevelopmentinmousemodels.Methods:PCRwasusedtoidentifyCBAmicewithdifferentgenotypes,i.e.WT,heterozygous(klotho+/-)orhomozygous(klotho-/-).Micephenotypeandweightwererecordedpostnatal25days(P-25)andauditorybrainstemresponses(ABR)wereusedtodetermineauditoryfunctionatP-60.Results:klotho-/-micetendedtohavesmallersize,lighterweightandhigherABRthresholdsatP-60,showingearlyonsetage-relatedhearingloss(ARHL).Conclusion:Heterozygousandhomozygousklothodeficientmiceexhibitdifferentdegreesofhearinglossatyoungage,withhomozygousmice(klotho-/-)showingmoreseverehearingloss.OurresultsindicatethatpersistedexpressionofklothoproteinintheinnerearmaypotentiallydelaytheonsetofARHLandplayanimportantroleintheprotectionofauditoryfunction.

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简介：ToobtaintherecombinantsolubleproteinoftheextracellularfragmentofhumanTRAILgeneandtoidentifyitsfunctionpreliminarily,thisgenefragmentwasamplifiedfromperipheralbloodmononu-clearcells(PBMC)byRT-PCRandclonedintovectorpGEM-T-Easyforsequenceanalysis.Theexpres-sionvectorpET-30a/TRAILwasthenconstructedbyDNArecombinationmethodwithaHis-taggeneatthefrontoftheTRAILfragment,andtherecombinantproteinwasexpressedinE.coliBL21(DE3).Meanwhile,theexpressedtargetproteinwaspurifiedwithNi-NTAchromatographycolumnandidentifiedbySDS-PAGEandWesternblotting.TheproliferationinhibitionactivityofTRAIL-HiswasdetectedbyMTTassay.PIstainingandWright-GiemsastainingwereusedtodetectthepresenceoftheTRAIL-in-ducedcellapoptosis.ItwasdemonstratedthatthetargetproteinexpressedinE.coliBL21showedthesamerelativemolecularmassasthattheproteinexpectedandcouldberecognizedbyboththeanti-TRAILpolyclonalantibodyandanti-Hismonoclonalantibody.Inaddition,thisproteincouldalsoinhibitprolif-erationofhumanlymphomacelllineJurkatcellsorinduceapoptosisofthiscellline.ItisapparentthatarecombinantsolubleTRAILproteinwithbiologicalactivityisobtainedandthisprospectivestudycanlaysolidfoundationforfurtherresearchonthebiologicalactivityandapplicationintheanti-tumortherapy.

简介：肿瘤immunoevasion是肿瘤房间在获得能力围绕主人免疫系统并且利用protumorigenic发炎的癌症immunosurveillance的一个先进阶段。T房间免疫球蛋白粘蛋白(提姆)基因家庭成员作为调整多重有免疫力的反应阶段并且维持有免疫力的动态平衡的批评检查点蛋白质出现了。积累的证据证明肿瘤房间利用提姆基因家庭成员躲避immunosurveillance，而提姆基因家庭成员便于发炎相关的肿瘤前进的预防。因此，在肿瘤前进澄清提姆基因家庭成员的相对贡献的全面分析可以阐明在癌症病人的immunosurveillance系统。

简介：AIM:Totransfectthecatcornealendothelialcells(CECs)withrecombinanthumanβ-nervegrowthfactorgeneadeno-associatedvirus(AAV-β-NGF)andtoobservetheeffectoftheexpressedβ-NGFproteinontheproliferationactivityofcatCECs.METHODS:TheendotheliumofcatcorneawastornunderthemicroscopeandrapidlycultivatedinDulbecco’smodifiedEagle’smedium(DMEM)toformsinglelayerCECsandthepassage2endothelialcellswereusedinthisexperiment.TherecombinanthumanAAV-β-NGFwasconstructed.TherecombinanthumanAAV-β-NGFwastransferredintocatCECsdirectly.Threegroupswereasfollowing:normalCECcontrolgroup,CEC-AAVcontrolgroupandrecombinantCECAAV-β-NGFgroup.Forty-eighthoursaftertransfection,thetotalRNAwasextractedfromtheCECbyTrizol.Theexpressionoftheβ-NGFtargetgenedetectedbyfluorescencequantitativepolymerasechainreaction;proliferationactivityofthetransfectedCECdetectedat48hbyMTTassay;thepercentageofG1cellsamongCECsaftertransfectwasdetectedbyflowcytometrymethod(FCM);cellmorphologywasobservedunderinvertedphasecontrastmicroscope.RESULTS:Thetornendotheliumculturetechniquerapidlycultivatedsinglelayercatcornealendothelialcells.Theself-designedprimersforthetargetgeneandreferencegenewereefficientandspecialconfirmedthroughelectrophoresisanalysisandDNAsequencing.Forty-eighthoursaftertransfect,thehumanβ-NGFgenemRNAdetectedbyfluorescencequantitativepolymerasechainreactionshowedthattherewasnosignificantdifferencebetweennormalCECcontrolgroupandCECAAVcontrolgroup(P>0.05);therewassignificantdifferencebetweentwocontrolgroupsandrecombinantCEC-AAV-β-NGFgroup(P<0.05).MTTassayshowedthattransfectofrecombinantAAV-β-NGFpromotedtheproliferationactivityofcatCEC,whiletherewasnosignificantdifferencebetweennormalCECcontrolgroupandCEC-AAVcontrolgroup(P>0.05).FCMresultshowedthatthepercentageofG1cellsinCECAAV-NGFgroupwas76.8%whi

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简介：Sincepigisanimportantlivestockspeciesworldwide,itsgeneexpressionhasbeeninvestigatedintensively,butrarelyinbrain.Inordertostudygeneexpressionprofilesinthepigcentralnervoussystem,wesequencedandanalyzed43,122highquality5′endexpressedsequencetags(ESTs)fromporcinecerebellum,cortexcerebrum,andbrainstemcDNAlibraries,involvingseveraldifferentprenatalandpostnataldevelopmentalstages.TheinitialESTswereassembledinto16,101clustersandcomparedtoproteinandnucleicaciddatabasesinGenBank.Ofthesesequences,30.6%clustersmatchedproteindatabasesandrepresentedfunctionknownsequences;75.1%hadsignificanthitstonucleicaciddatabasesandpartialrepresentedknownfunction;73.3%matchedknownporcineESTs;and21.5%hadnomatchestoanyknownsequencesinGenBank.WeusedthecategoriesdefinedbytheGeneOntologytosurveygeneexpressionintheporcinebrain.

简介：抗菌剂肽是有抗菌剂活动的多肽。从中国虾(FenneropenaeusChinensis)的抗菌剂肽基因Np3和Np5集成于OryzasativaL。subsp。装饰用的梨树cv。由Agrobacterium的Aichiashahi调停了转变系统。PCR分析证明Np3和Np5的积极比率分别地在T0产生是36%和45%。RT-PCR分析证明抗菌剂肽基因在T1产生被表示，并且在转基因的植物和非转基因的植物之间的农学的特点地没有明显的差别。四Np3和Np5在T1产生的转基因的线与Xanthomonasoryzaepv被接种。oryzae紧张CR4，和所有四根转基因的线显著地提高了抵抗到紧张CR4引起的细菌的老家。Np5转基因的线也显示出更高的抵抗到紧张JS97-2，Zhe173和OS-225引起的细菌的老家。有Np5基因力量的转基因的线拥有宽广光谱抵抗到米饭，这被建议细菌的老家。