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Transient loading of CD34+ hematopoietic progenitor cells with polystyrene nanoparticles
被引:5
|作者:
Deville, Sarah
[1
,2
]
Hadiwikarta, Wahyu Wijaya
[1
]
Smisdom, Nick
[1
,2
]
Wathiong, Bart
[1
,3
]
Ameloot, Marcel
[2
]
Nelissen, Inge
[1
]
Hooyberghs, Jef
[1
,3
]
机构:
[1] Flemish Inst Technol Res, VITO, Mol, Belgium
[2] Hasselt Univ, Biomed Res Inst, Diepenbeek, Belgium
[3] Hasselt Univ, Theoret Phys, Diepenbeek, Belgium
来源:
关键词:
nanoparticles;
hematopoietic progenitor cells;
dendritic cells;
uptake;
release;
IRON-OXIDE;
PERIPHERAL-BLOOD;
CELLULAR UPTAKE;
EXOCYTOSIS;
ENDOCYTOSIS;
SIZE;
THERAPIES;
TRACKING;
MODEL;
PLGA;
D O I:
10.2147/IJN.S119407
中图分类号:
TB3 [工程材料学];
学科分类号:
0805 ;
080502 ;
摘要:
CD34(+) hematopoietic progenitor cells (HPCs) offer great opportunities to develop new treatments for numerous malignant and non-malignant diseases. Nanoparticle (NP)-based strategies can further enhance this potential, and therefore a thorough understanding of the loading behavior of HPCs towards NPs is essential for a successful application. The present study focusses on the interaction kinetics of 40 nm sized carboxylated polystyrene (PS) NPs with HPCs. Interestingly, a transient association of the NPs with HPCs is observed, reaching a maximum within 1 hour and declining afterwards. This behavior is not seen in dendritic cells (CD34-DCs) differentiated from HPCs, which display a monotonic increase in NP load. We demonstrate that this transient interaction requires an energy-dependent cellular process, suggesting active loading and release of NPs by HPCs. This novel observation offers a unique approach to transiently equip HPCs. A simple theoretical approach modeling the kinetics of NP loading and release is presented, contributing to a framework of describing this phenomenon.
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页码:459 / 472
页数:14
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