Endogenous Thrombospondin-1 Regulates Leukocyte Recruitment and Activation and Accelerates Death from Systemic Candidiasis 英文参考文献.docVIP
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Endogenous Thrombospondin-1 Regulates Leukocyte Recruitment and Activation and Accelerates Death from Systemic Candidiasis 英文参考文献
EndogenousThrombospondin-1RegulatesLeukocyte
RecruitmentandActivationandAcceleratesDeathfrom
SystemicCandidiasis
GemaMartin-Manso,DhammikaH.M.L.P.Navarathna,SusanaGalli,DavidR.Soto-Pantoja,
SvetlanaA.Kuznetsova¤,MariaTsokos,DavidD.Roberts*
LaboratoryofPathology,CenterforCancerResearch,NationalCancerInstitute,NationalInstitutesofHealth,Bethesda,Maryland,UnitedStatesofAmerica
Abstract
DisseminatedCandidaalbicansinfectionresultsinhighmorbidityandmortalitydespitetreatmentwithexistingantifungal
drugs.Recentstudiessuggestthatmodulatingthehostimmuneresponsecanimprovesurvival,butspecifichosttargetsfor
accomplishingthisgoalremaintobeidentified.Theextracellularmatrixproteinthrombospondin-1isreleasedatsitesof
tissueinjuryandmodulatesseveralimmunefunctions,butitsroleinC.albicanspathogenesishasnotbeeninvestigated.
Here, we show that mice lacking thrombospondin-1 have an advantage in surviving disseminated candidiasis and more
efficientlycleartheinitialcolonizationfromkidneysdespiteexhibitingfewerinfiltratingleukocytes.Byexamininglocaland
systemic cytokine responses to C. albicans and other standard inflammatory stimuli, we identify a crucial function of
phagocytes in this enhanced resistance. Subcutaneous air pouch and systemic candidiasis models demonstrated that
endogenousthrombospondin-1enhancestheearlyinnateimmuneresponseagainstC.albicansandpromotesactivationof
inflammatorymacrophages(induciblenitricoxidesynthase+,IL-6high,TNF-ahigh,IL-10low),releaseofthechemokinesMIP-2,
JE, MIP-1a, and RANTES, and CXCR2-driven polymorphonuclear leukocytes recruitment. However, thrombospondin-1
inhibitedthephagocyticcapacityofinflammatoryleukocytesinvivoandinvitro,resultinginincreasedfungalburdeninthe
kidney and increased mortality in wild type mice. Thus, thrombospondin-1 enhances the pathogenesis of disseminated
candidiasisbycreatinganimbalanceinthehostimmuneresponsethatultimatelyleadstoreducedphagocyticfunction,
impaired fungal clearance, and increased mortality. Conversely, inhibitors
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