Propofol exerts its antiinflammatory effect in Alveolar type II epithelial cells through downreg.docx
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Propofol exerts its antiinflammatory effect in Alveolar type II epithelial cells through downreg.docx
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PropofolexertsitsantiinflammatoryeffectinAlveolartypeIIepithelialcellsthroughdownreg
Propofolexertsitsanti-inflammatoryeffectinAlveolartype
epithelialcellsthroughdownregulationofCD14andTLR4expression
LingMa,WeiminChen,XiuyingWu,LingxinMeng,YujiFujino
Authors:
LingMa,M.D.1,XiuyingWu,M.D,Ph.D2,WeiminChen,M.D,Ph.D3,YujiFujino,M.D,Ph.D4
1.Lecturer,DepartmentofAnesthesiology,ShengjingHospitalofChinaMedicalUniversity,Shenyang,China
2.AssociateProfessor,DepartmentofAnesthesiology,ShengjingHospitalofChinaMedicalUniversity,Shenyang,China
3.Professor,DepartmentofAnesthesiology,ShengjingHospitalofChinaMedicalUniversity,Shenyang,China
4.AssociateProfessor,DepartmentofAnesthesiologyandIntensiveCareMedicine,OsakaUniversityMedicalSchool,Osaka,Japan
Correspondingauthor:
WeiminChen.
Mailingaddress:
DepartmentofAnesthesiology,No.36SanhaoStreet,HepingDistrict,Shenyang,110004,China.
Phone:
+86-13386861177Email:
chenwm@sj-hospital.org
Runningtitle:
propofolandalveolartype
epithelialcell
Summary
Background:
WeinvestigatedwhetherLPSinducedinflammationinATIIisthroughCD14andTLR4andtheeffectofdifferentdosageofpropofolontheinflammationinprimaryculturedratalveolarepithelialtype
(AT
)cells.
Methods:
TheculturedAT
cellswererandomlyassignedtooneofthefollowingfivegroups:
GroupC:
AT
cellsinuntreatedgroup(control)wasculturedintheabsenceofpropofolandLPS;GroupLPS:
treatedwith1μg.-1mlLPS;GroupP1:
treatedwith1μ.ml-1LPSand25μMpropofol;GroupP2:
treatedwith1μg.ml-1LPSand50μMpropofol;GroupP3:
treatedwith1μg.ml-1LPSand100μMpropofol.AT
cellsinuntreatedandpropofolcontrolgroupswereculturedat37°Cfor3h.CD14andTLR4mRNAweredetectedusingreal-timePCR.WesternblotwereusedtodetectCD14andTLR4proteinexpression.CD14andTLR4expressionontheAT
cellswereimagedusingimmunofluorescence.TNF-αproductionweredeterminedusingELISAkit.
Results:
LPSstimulationresultedinanincreasedCD14andTLR4expressionandincreasedTNF-αproductioninAT
cells.Propofol,atconcentrations
50µM,significantly(P<0.05)anddose-dependentlydecreasedCD14andTLR4mRNAexpressionandproteinexpressioninAT
cells.ThiswasaccompaniedbydecreasesinTNF-αproduction(P<0.05).
Conclusion:
Theseresultssuggestthatpropofol,atclinicalrelevantconcentrations,canreduceinflammatoryresponseinLPS-inducedAT
cellsinjurythroughdownregulationofCD14andTLR4expression.
Keywords:
propofol;alveolartype
epithelialcell;CD14;Tolllikereceptor-4
Introduction:
Thelungrepresentsasitefortheinvasionofvariousbacteriaorbacterialproducts.Alongwithalveolarmacrophages,pulmonaryepithelialcellsarethefirstcellstobechallengedbypathogenicmicroorganisms.ratalveolarepithelialtype
(AT
)cellssynthesizeandsecretesurfactant,controlthevolumeandcompositionoffluidinthealveolarspace,andproliferateanddifferentiateintoalveolartypeIepithelialcellsafterlunginjurytomaintaintheintegrityofthealveolarlining1,2.Recently,therehavebeenpublicationsreportingtheinvolvementofAT
inmodulatingthedevelopmentofinflammatoryreactionswithinthealveolus3.AT
secretechemokinesinresponsetoinflammatorystimuliinvitro,suggestingapotentialphysiologicroleinacuteinflammatorylunginjury4,5.
Lipopolysaccharide(LPS)triggersaphysicalassociationbetweenclusterofdifferentiation14(CD14)andTolllikereceptor4(TLR4)6,7.InflammatoryresponsetoendotoxinislargelymediatedthroughCD14andTLR48,9.TheactivationofCD14andTLR4leadstoproinflammatorycascadeincludingtheexpressionofproinflammatorymediators,suchasTNF-α.CD14andTLR4havebeenfoundonAT
10,11andcouldthusplayanimportantroleintheinnateimmuneresponseatthealveolarsurfacearea.
Littleisknownabouttheinteractionofgenerallyusedintravenousanestheticpropofol(2,6-diisopropylphenol)withATII.OurgoalistoinvestigatewhetherLPSinducedinflammationinATIIisthroughCD14andTLR4andtheeffectofdifferentdosageofpropofolontheinflammation.
MethodsandMaterials
Isolationofalveolarepithelialcellandprimaryculture
ATIIwereisolatedfrommaleSPFdegreeWistarrats(180-250g),followingtheprotocolaccordingtothemethodofRichardetal12.Briefly,afterintraperitonealsodiumpentobarbital(60mg.kg-1)andheparin(400U.kg-1),thethoraciccavitywasopenedandtheinferiorvenacavawascut.Thelungswereperfusedviatherightatriumwithsterilesalineandinflatedsimultaneouslywithair.Afterremovalfromthethoraciccavity,theywerewashed6timeswithnormalsalineanddigestedenzymaticallywithtypsin.Thelungswerethenmincedinfetalbovineserum(FBS)andDNase
(Roche),andtheresultingsuspensionwasfilteredthrough150μmand30μmmeshonce.ThecellmixturewaspurifiedbycentrifugationonadiscontinuousPercollgradient(density1.089and1.04,400g,20min).Theinterfacewascollectedandafterrewashingthecellswereseededonto6-wellculturedishesatadensityof1×106cells/dishinDulbecco'smodifiedEaglemedium(DMEM)with10%inactivatedFBS,penicillin(100U.ml-1),streptomycin(100μg.ml-1)at37℃inthehumidifiedatmosphereof95%air/5%CO2andculturedfor18-20hours.
Characterizationoftype
pneumocyte
AlkalinePhosphataseHistochemicalStaining
AlkalinephosphatasestainingservedtoidentifyATIIcellsinprimaryculturedcellsgrownonglasscoverslips.Briefly,thecellswerefixedfor15minatroomtemperaturein4%paraformaldehydesolution,rinsedfor1minindistilledwater,andair-dried.FixedcellswereincubatedwithBCIP/NBTstain(SigmaChemical,StLouis,Mo)for10minatroomtemperature.Thesampleswerethenrinsedwithdistilledwaterfor1minandair-dried.Thecellswerecounterstainedwith0.1%neutralredsolution(Sigma)for1minatroomtemperature,rinsedfor1min,air-dried,andphotographedunderlightmicroscopy.Bluestainingidentifiedcellswithhighalkalinephosphataseactivity,whereasothercells,suchasmacrophages,werecounterstainedinred.
Transmissionelectronmicroscopy
Cellswerefixedin2.5%glutaraldehyde,washedthreetimesin0.1Mphosphatebufferedsaline(PBS)andseriallydehydratedinacetoneandembeddedinEpon812.Ultrathinsections(70nm)wereexaminedwithatransmissionelectronmicroscope(JEM-1200EX,JEOL,Tokyo,Japan).
Experimentaldesign
TheculturedAT
cellswererandomlyassignedtooneofthefollowingfivegroups:
GroupC:
AT
cellsinuntreatedgroup(control)wasculturedfor3hintheabsenceofpropofol(AstraZeneca,Basiglio,Italy)andLPS(E.ColiO55:
B5,Sigma);GroupLPS:
treatedwith1μg.-1mlLPSfor3h;GroupP1:
treatedwith1μ.ml-1LPSand25μMpropofolfor3h;GroupP2:
treatedwith1μg.ml-1LPSand50μMpropofolfor3h;GroupP3:
treatedwith1μg.ml-1LPSand100μMpropofolfor3h.
RealTimePCR
TotalRNAwasextractedbyTRIzolreagent(Invitrogen,Carlsbad,CA).RealtimePCRswereconductedwithSYBRPrimeScriptTMRT-PCRkit(Cat.no.DRR063S,TaKaRaBiotechnology,Dalian,China)accordingtothemanufacturer’sinstructions.Briefly,totalRNA(500ng)wasreverse-transcribedintocDNAusing0.5μlPrimeScriptRTEnzymeMix
0.5μlRandom6mers.QuantitativerealtimePCRwasdoneusinganABIPRISM®7500Real-TimePCRSystem(PEAppliedBiosystems,FosterCity,CA).Thereactionswerecarriedoutonmultiple8-wellstripes.GAPDHwasamplifiedonthesameplatesandusedtonormalizethedata.Thereactionvolumewas25μlcontaining12.5μloftheSYBRPremixEXTaq,0.5μlofROXreferenceDye
2.5μleachof2μMforwardandreverseprimers,5μlofRNasefreewater,and2μlofthecDNAsamples.Real-timePCRswereperformedintriplicateforeachsampleandatleast3differentsetsofcellpreparationswereused.Thethermalcyclingconditionsusedwere:
95℃for10sfollowedby40cyclesat95℃for5s,60℃for34s.PCRproductswereheatedto95℃for15s,annealedat60℃for1minandthenheatedfrom60℃to95℃for15stoobtainmeltingcurve.DissociationcurveanalysiswasperformedforeachgenetoensurethespecificityofPCRproducts.Serialdilutions(10-fold)ofoneofthesampleswereusedtogeneratethestandardcurveforeachPCR.AllsenseandantisenseprimersweresuppliedbySangon(Shanghai,China).Theoligonucleotidesprimersusedforreal-timePCRwere:
ratCD14:
forwardATTCCCGACCCTCCAAGT;reverseCCAGCAGTATCCCGCAGT;ratTLR4:
forwardGAGGACTGGGTGAGAAACGA;reverseGAAACTGCCATGTCTGAGCA;ratGAPDH:
forwardATGTTCCAGTATGACTCCACTCACG;reverseGAAGACACCAGTAGACTCCACGACA.
Immunoblotting
Cellswerelysedusingacommerciallyavailablekit(KGP250;NanjingKeygenBiotechCo.Ltd.,Nanjing,China).ProteinconcentrationwasdeterminedusingtheEasyQuantproteinassaykit(Cat.no.DQ101,TransGenBiotechCo.Ltd.,Beijing,China)andboiledfor5minat100℃.EachvesselhomogenatewasdilutedwithPBStoobtainthesameproteinconcentration.Then20μgofproteinperlanewasseparatedona10%SDS-polyacrylamidegelsandtransferredtoanitrocellulosemembrane(Bio-Rad,Hercules,CA).Thetransferswereblockedovernightwith5%dryskimmilkpower.Themembraneswereincubatedwithanti-CD14(sc-9150),anti-TLR4(sc-16240)oranti-β-actin(sc-47778;allSantaCruzBiotechnology,CA)antibodiesat1:
200dilutionsfor2hat37℃.AfterbeingwashedinPBS3times,themembraneswereincubatedwith1:
2000horseradishperoxidase-conjugatedanti-rabbit,-goat,or-mouseIgGs(Pierce,Rockford,IL)for1hatroomtemperature.Theblotswerewashedagain.Theindividualtargetproteinswere
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