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Brain Miffed by Macrophage Migration Inhibitory Factor英文文献资料
HindawiPublishingCorporation
InternationalJournalofCellBiology
Volume2012,ArticleID139573,11pages
doi:10.1155/2012/139573
ReviewArticle
BrainMiffedbyMacrophageMigrationInhibitoryFactor
NicE.Savaskan, G¨unterFingerle-Rowson, MichaelBuchfelder, andIlkerY.Ey¨upoglu
1 2 1 1
1
2
DepartmentofNeurosurgery,UniversityofErlangen-Nuremberg,Schwabachanlage6,91054Erlangen,Germany
ClinicIforInternalMedicine,UniversityHospitalCologne,KerpenerStra?e62,50924Cologne,Germany
CorrespondenceshouldbeaddressedtoNicE.Savaskan,Nicolai.savaskan@uk-erlangen.deand
IlkerY.Ey¨upoglu,ilker.eyupoglu@uk-erlangen.de
Received18May2012;Revised6July2012;Accepted12July2012
AcademicEditor:PierGiorgioMastroberardino
Copyright?2012NicE.Savaskanetal. This is an open access article distributed under the Creative Commons Attribution
License,whichpermitsunrestricteduse,distribution,andreproductioninanymedium,providedtheoriginalworkisproperly
cited.
Macrophagemigrationinhibitoryfactor(MIF)isacytokinewhichalsoexhibitsenzymaticpropertieslikeoxidoreductaseand
tautomerase.MIFplaysapivotalroleininnateandacquiredimmunityaswellasintheneuroendocrineaxis.Sinceitisinvolved
in the pathogenesis of acute and chronic in?ammation, neoangiogenesis, and cancer, MIF and its signaling components are
consideredsuitabletargetsfortherapeuticinterventioninseveral?eldsofmedicine.Inneurodegenerativeandneurooncological
diseases,MIFisahighlyrelevant,butstillahardlyinvestigatedmediator.MIFoperatesviaintracellularprotein-proteininteraction
aswellasinCD74/CXCR2/CXCR4receptor-mediatedpathwaystoregulateessentialcellularsystemssuchasredoxbalance,HIF-
1,andp53-mediatedsenescenceandapoptosisaswellasmultiplesignalingpathways.Actingasanendogenousglucocorticoid
antagonist, MIF thus represents a relevant resistance gene in brain tumor therapies. Alongside this dual action, a functional
homolog-annotated D-dopachrome tautomerase/MIF-2 has been uncovered utilizing the same cell su
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