Journal of Leukocyte Biology: An Official Publication of the Reticuloendothelial Society | |
Immunomodulatory and immunotoxic effects of bilirubin: molecular mechanisms | |
关键词: unconjugated bilirubin; p38MAPK; CD95; Bax; oxidative stress; | |
DOI : 10.1189/jlb.0211070 | |
学科分类:生理学 | |
来源: Federation of American Societies for Experimental Biology | |
【 摘 要 】
TheimmunomodulatoryandimmunotoxiceffectsofpurifiedUCBhavenotbeenevaluatedpreviouslyatclinicallyrelevantUCBconcentrationsandUCB:BSAratios.TodelineatethemolecularmechanismofUCB‐inducedimmunomodulation,immunecellswereexposedtoclinicallyrelevantconcentrationsofUCB.ItinhibitedLPS‐inducedBcellproliferationandcytokineproductionfromsplenicmacrophages.UCB(≥25μM)wastoxictounfractionatedsplenocytes,splenicTcells,Bcells,macrophages,LPS‐stimulatedCD19+Bcells,humanPBMCs,andRBCs.PurifiedUCBalsowasfoundtobetoxictosplenocytesandhumanPBMCs.UCBinducednecrosisandapoptosisinsplenocytes.UCBactivatedtheextrinsicandintrinsicpathwaysofapoptosis,asreflectedbythemarkers,suchasCD95,caspase‐8,Bax,MMP,cytoplasmicCa+2,caspase‐3,andDNAfragmentation.UCBdepletedGSHandactivatedp38MAPK.NAC,caspaseinhibitors,andp38MAPKinhibitorattenuatedtheUCB‐inducedapoptosis.Invivoadministrationof≥25mg/kbwUCBinducedatrophyofspleen,depletionofbonemarrowcells,andleukopeniaanddecreasedlymphocytecountandtheTandBcellresponsetomitogens.UCBadministrationtomiceledtoinductionofoxidativestress,activationofp38MAPK,andcelldeathinsplenocytes.TheseparameterswereattenuatedbytheinjectionofNACandthep38MAPKinhibitor.OurresultsdemonstrateforthefirsttimethatclinicallyrelevantconcentrationsofUCBinduceapoptosisandnecrosisinimmunecellsbydepletingcellularGSH.Thesefindingsshouldproveusefulinunderstandingtheimmunosuppressionassociatedwithhyperbilirubinemia...
【 授权许可】
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