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.
引用
收藏
页码:459 / 472
页数:14
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