人外周血巨噬细胞培养及功能鉴定-林炜明

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doi10.3969/j.issn.1000-484X.2015.01.018①②364000R292.12A1000-484X201501-0086-04①JKNo.JK2011053、2013N0026。②364000。1976-E-mailwmlin925@126.com。PBMC。CD14+10%AB10ng/mlM-CSFIMDMCD14+。CD14+CD1410%CD1485.8%。740~45μmRaji。CD14+。CultureandfunctionalidentificationofmacrophagesfromhumanperipheralbloodLINWei-MingDAIAi-LingYinHui-FangYANGXiao-Yan.CollegeofLifeSciencesofLongyanUniversityLongyan364000ChinaAbstractObjectiveToisolatemonocytesfromhumanperipheralbloodmononuclearcellsPBMCinducemacrophagesandidentifythefunctionofmacrophages.MethodsMonocyteswereisolatedfromPBMCusingmagneticactivatedcellsortingMACSanti-CD14microbead.SortedCD14+andCD14-cellswerecheckedbyflowcytometertoevaluatetheefficiencyofsorting.ThesortedCD14+cellswereculturedinIMDMmediawith10%humanABserumand10ng/mlM-CSFfor7daystogeneratemacrophageswhichwereidentifiedbymorphologicalfeaturesandphagocytosisfunction.ResultsAhighpurityofmonocyteswasobtainedbyMACSanti-CD14microbead.ThepercentageofCD14+cellswas10%and85.8%beforeandaftersortingrespectively.Themacrophageswereapproximately40-45μminmaximumdiameterandhadthefriedeggcolonymorphologicalfeaturesafter7daysculture.ThelymphomaRajicellswereefficientlyengulfedbymacrophages.ConclusionThehighpurityofCD14+monocytesisisolatedfromPBMCandmonocyte-derivedmacrophagesefficientlyengulfedlymphomacells.KeywordsMacrophagesMagneticactivatedcellsortingCultureFunctionalidentification-。。1。M-CSF2。CD14、、CD1434。CD14+。11.1IMDM、、ABTrypLELifeTechnologyM-CSFeBiosciencesPrimocinInvivogenCD14CD14cloneMoP9APCEasySepStemcellTechnol-ogies。682015311.2FicollPBMC2%FBSPBSPBMCPBMCDNaseⅠ15min30μm2.0×108PBMCCD14200μlEasySep15min100μlEasySep10min5min。2。1.3PBMC、CD14+5×1052.5μlCD14-APCcloneMoP9IgG4℃30minCD14CD14。1.410%AB10ng/mlM-CSFIMDM8ml10cmCD14+5×10637℃、5%CO27d。1、3、6、、。1.5Raji1.5.1CFSERaji1.0×106Raji0.5μmol/LCFSEPBS2minFBSFBS10%37℃10minCFSERaji。1.5.27PBSTrypLE15~20min1.0×106/ml。CFSERaji2.0×106/ml。50μl1∶29637℃、5%CO22h1μlCD14-APC4℃30min。22.11CD14PBMC10%CD14CD1485.8%CD14CD140.3%。CD14+。2.2CD14+CD14+10%AB10ng/mlM-CSFIMDM7d24h2A。31CD14Fig.1FlowcytometrygraphofpurityanalysisofCD14positivecellsNoteCD14expressionwasquantifiedflowcytometricanalysisusingCD14-APCantibodycloneMoP9.Blacklinesrepresentisotypecontrols.RedlinesrepresentA.PBMCbeforesortingB.NegativelyselectedcellsC.Positivelyselectedcells.7812Fig.2MorphologicalfeaturesofmacrophagesNoteMacrophagesculturedfor1dayA3daysB6daysC.3Fig.3FlowcytometrygraphofphagocytosisfunctionofmacrophageNoteA.MacrophagesbeforephagocytosisB.Macrophagesafterphago-cytosis2B。640~45μm2C。2.37CD14CD14+46%。56。CFSERaji2hCD14-APC3。82%CD1483%CD14+Raji。3-、2。3。7。CD14CD14CD1410%85.8%。CD14CD14BA-8CD14+MoP9CD14CD14CD14。GM-CSF、IL-48M-CSF2M-CSFROSSHP1PI3K/AKT/9。10。10%AB10ng/mlM-CSF88201531。76。CD14+7dTrypLETrypsin15~20minTrypLETrypsin。7CD14CD14CD14。5。Erbel4CD14CD45RO。。RajiRaji83%CD14+Raji。11。RajiCD47FcCD47Fc12。CD14+、。1.-J.2014301126-132.2GeissmannFManzMGJungSetal.DevelopmentofmonocytesmacrophagesanddendriticcellsJ.Science20103275966656-661.3ChengSMChangSJTsaiTNetal.Differentialexpressionofdis-tinctsurfacemarkersinearlyendothelialprogenitorcellsandmon-ocyte-derivedmocrophagesJ.GeneExpr201316115-24.4ErbelCRuppGHelmesCMetal.Aninvitromodeltostudyhet-erogeneityofhumanmacrophagedifferentiationandpolarizationJ.JVisExp201376e50332.5KangJWChoiSCChoMCetal.Aproinflammatorycytokinein-terleukin-32βpromotestheproductionofananti-inflammatorycy-tokineinterleukin-10J.Immunology20091281e532-540.6.DC-STAMPJ.2013295474-480.7.J.201329188-92.8DelirezhNMajediLRezaeiSAetal.Generationofmaturemono-cyte-deriveddendriticcellsinthepresenceofheparinandmono-cyteconditionedmediumphenotypicandfunctionalcomparisonJ.IranBiomedJ201115379-84.9ChoiHKKimTHJhonGetal.ReactiveoxygenspeciesregulateM-CSF-inducedmoncyte/macophageproliferationthroughSHP1oxidationJ.CellSignal201123101633-1639.10HodreaJDeményMAMajaiGetal.Transglutaminase2isex-pressedandactiveonthesurfaceofhumanmonocye-derivedden-driticcellsandmacrophagesJ.ImmunolLett2010130174-81.11.J.2011322197-203.12ChaoMPAlizadehAATangCetal.Anti-CD47antibodysyner-gizeswithrituximabtopromotephagocytosisanderadicatenon-hodgkinlymphomaJ.Cell20101425699-713.2014-08-202014-09-10981

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