Surface modification of microparticles causes differential uptake responses in normal and tumoral human breast epithelial cells

被引:66
|
作者
Patino, Tania [1 ]
Soriano, Jorge [1 ]
Barrios, Lleonard [1 ]
Ibanez, Elena [1 ]
Nogues, Carme [1 ]
机构
[1] Univ Autonoma Barcelona, Fac Biociencies, Dept Biol Celulular Fisiol & Immunol, Unitat Biol Celulular, Bellaterra 08139, Spain
来源
SCIENTIFIC REPORTS | 2015年 / 5卷
关键词
CELLULAR UPTAKE; DRUG-DELIVERY; PLASMID DNA; NANOPARTICLES; POLYETHYLENEIMINE; INTERNALIZATION; PARTICLES; SIZE; MICROCAPSULES; MECHANISMS;
D O I
10.1038/srep11371
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The use of micro-and nanodevices as multifunctional systems for biomedical applications has experienced an exponential growth during the past decades. Although a large number of studies have focused on the design and fabrication of new micro-and nanosystems capable of developing multiple functions, a deeper understanding of their interaction with cells is required. In the present study, we evaluated the effect of different microparticle surfaces on their interaction with normal and tumoral human breast epithelial cell lines. For this, AlexaFluor488 IgG functionalized polystyrene microparticles (3 mu m) were coated with Polyethyleneimine (PEI) at two different molecular weights, 25 and 750 kDa. The effect of microparticle surface properties on cytotoxicity, cellular uptake and endocytic pathways were assessed for both normal and tumoral cell lines. Results showed a differential response between the two cell lines regarding uptake efficiency and mechanisms of endocytosis, highlighting the potential role of microparticle surface tunning for specific cell targeting.
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页数:12
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