Journal of Leukocyte Biology: An Official Publication of the Reticuloendothelial Society | |
Attenuation of HIV‐1 replication in macrophages by cannabinoid receptor 2 agonists | |
关键词: neuroinflammation; JWH133; CXCR4; CCR5; encephalitis; CB2; | |
DOI : 10.1189/jlb.1012523 | |
学科分类:生理学 | |
来源: Federation of American Societies for Experimental Biology | |
【 摘 要 】
InfiltratingmonocytesandmacrophagesplayacrucialroleintheprogressionofHIV‐1infectionintheCNS.PreviousstudiesshowedthatactivationoftheCB2canattenuateinflammatoryresponsesandaffectHIV‐1infectivityinTcellsandmicroglia.Here,wereportthatCB2agonistscanalsoactasimmunomodulatorsonHIV‐1‐infectedmacrophages.First,ourfindingsindicatedthepresenceofelevatedlevelsofCB2expressiononmonocytes/macrophagesinperivascularcuffsofpostmortemHIV‐1encephaliticcases.InvitroanalysisbyFACSofprimaryhumanmonocytesrevealedastep‐wiseincreaseinCB2surfaceexpressioninmonocytes,MDMs,andHIV‐1‐infectedMDMs.Wenexttestedthenotionthatup‐regulationofCB2mayallowfortheuseofsyntheticCB2agonisttolimitHIV‐1infection.TwocommerciallyavailableCB2agonists,JWH133andGP1a,andaresorcinol‐basedCB2agonist,O‐1966,wereevaluated.ResultsfrommeasurementsofHIV‐1RTactivityintheculturemediaof7day‐infectedcellsshowedasignificantdecreaseinRTactivitywhentheCB2agonistwaspresent.Furthermore,CB2activationalsopartiallyinhibitedtheexpressionofHIV‐1pol.CB2agonistsdidnotmodulatesurfaceexpressionofCXCR4orCCR5detectedbyFACS.WespeculatethatthesefindingsindicatethatpreventionofviralentryisnotacentralmechanismforCB2‐mediatedsuppressioninviralreplication.However,CB2mayaffecttheHIV‐1replicationmachinery.Resultsfromasingle‐roundinfectionwiththepseudotypedvirusrevealedamarkeddecreaseinHIV‐1LTRactivationbytheCB2ligands.Together,theseresultsindicatethatCB2mayofferameanstolimitHIV‐1infectioninmacrophages...
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