Different Capacity of Monocyte Subsets to Phagocytose Iron-Oxide Nanoparticles 英文参考文献.docVIP
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Different Capacity of Monocyte Subsets to Phagocytose Iron-Oxide Nanoparticles 英文参考文献
DifferentCapacityofMonocyteSubsetstoPhagocytose
Iron-OxideNanoparticles
MarcusSettles1,MartinEtzrodt2,KatjaKosanke1,MatthiasSchiemann3,AlexanderZimmermann4,
ReinhardMeier1,RickmerBraren1,ArminHuber1,ErnstJ.Rummeny1,RalphWeissleder2,FilipK.
Swirski2,MoritzWildgruber1,2*
1Institutfu¨rRadiologie,KlinikumRechtsderIsar,TechnischeUniversita¨t Mu¨nchen,Munich,Germany,2CenterforSystemsBiology,MassachusettsGeneralHospitaland
HarvardMedicalSchool,Boston,Massachusetts,UnitedStatesofAmerica,3Institutfu¨rmedizinischeMikrobiologie,ImmunologieundHygiene,KlinikumRechtsderIsar,
Technische Universita¨t Mu¨nchen and Clinical Cooperation Group ‘‘Antigen-Specific Immunotherapy’’, Helmholtzzentrum Mu¨nchen, Munich, Germany, 4Klinik und
Poliklinikfu¨rGefa¨?chirurgie, KlinikumRechtsderIsar,TechnischeUniversita¨t Mu¨nchen,Munich,Germany
Abstract
Objective: To explore the capacity of human CD14+CD16++ and CD14++CD16- monocytes to phagocyte iron-oxide
nanoparticlesinvitro.
Methods:Humanmonocyteswerelabeledwithfourdifferentmagneticnanoparticlepreparations(Ferumoxides,SHU555C,
CLIO-680, MION-48) exhibiting distinct properties and cellular uptake was quantitatively assessed by flow cytometry,
fluorescence microscopy, atomic absorption spectrometry and Magnetic Resonance Imaging (MRI). Additionally we
determinedwhethercellularuptakeofthenanoparticlesresultedinphenotypicchangesofcellsurfacemarkers.
Results: Cellular uptake differed between the four nanoparticle preparations. However for each nanoparticle tested,
++
+
++
CD14 CD16- monocytes displayed a significantly higher uptake compared to CD14 CD16 monocytes, this resulted in
significantly lower T1 and T2 relaxation times of these cells. The uptake of iron-oxide nanoparticles further resulted in a
remarkable shift of expression of cell surface proteins indicating that the labeling procedure affects the phenotype of
+
CD14 CD16 andCD14 CD16-monocytesdifferently.
++
++
Conclusion: Human monocyte subsets internalize different magnetic n
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