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Surface Modification of Microparticles Causes Differential Uptake Responses in Normal and Tumoral Human Breast Epithelial Cells

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Journal Sci Rep
Specialty Science
Date 2015 Jun 13
PMID 26068810
Citations 29
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Abstract

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 μm) 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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References
1.
Sanna V, Pala N, Sechi M . Targeted therapy using nanotechnology: focus on cancer. Int J Nanomedicine. 2014; 9:467-83. PMC: 3896284. DOI: 10.2147/IJN.S36654. View

2.
Barr D, Ostermeyer-Fay A, Matundan R, Brown D . Clathrin-independent endocytosis of ErbB2 in geldanamycin-treated human breast cancer cells. J Cell Sci. 2008; 121(Pt 19):3155-66. PMC: 2707784. DOI: 10.1242/jcs.020404. View

3.
Patino T, Mahajan U, Palankar R, Medvedev N, Walowski J, Munzenberg M . Multifunctional gold nanorods for selective plasmonic photothermal therapy in pancreatic cancer cells using ultra-short pulse near-infrared laser irradiation. Nanoscale. 2015; 7(12):5328-37. DOI: 10.1039/c5nr00114e. View

4.
Gratton S, Ropp P, Pohlhaus P, Luft J, Madden V, Napier M . The effect of particle design on cellular internalization pathways. Proc Natl Acad Sci U S A. 2008; 105(33):11613-8. PMC: 2575324. DOI: 10.1073/pnas.0801763105. View

5.
Macia E, Ehrlich M, Massol R, Boucrot E, Brunner C, Kirchhausen T . Dynasore, a cell-permeable inhibitor of dynamin. Dev Cell. 2006; 10(6):839-50. DOI: 10.1016/j.devcel.2006.04.002. View