Tracking cell proliferation using a nanotechnology-based approach

被引:9
|
作者
Altea-Manzano, Patricia [1 ,3 ]
Diego Unciti-Broceta, Juan [3 ]
Cano-Cortes, Victoria [1 ,2 ]
Paz Ruiz-Blas, Maria [1 ,2 ]
Valero-Grianan, Teresa [1 ,2 ]
Jose Diaz-Mochon, Juan [1 ,2 ]
Sanchez-Martin, Rosario [1 ,2 ]
机构
[1] Univ Granada, GENYO Pfizer, Junta Andalucia Ctr Genom & Oncol Res, Hlth Sci Technol Pk PTS, Ave Ilustrac 114, Granada 18016, Spain
[2] Univ Granada, Dept Med & Organ Chem, Campus Cartuja S-N, E-18071 Granada, Spain
[3] NanoGet SL Granada, Hlth Sci Technol Pk PTS, R&D Dept, Ave Innovac 1,Edificio BIC, Granada 18016, Spain
关键词
cell proliferation; cell tracking; flow cytometry; fluorescent nanoparticles; nanofection; POLYSTYRENE NANOPARTICLES; NANO;
D O I
10.2217/nnm-2017-0118
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aim: To develop an efficient nanotechnology fluorescence-based method to track cell proliferation to avoid the limitations of current cell-labeling dyes. Material & methods: Synthesis, PEGylation, bifunctionalization and labeling with a fluorophore (Cy5) of 200 nm polystyrene nanoparticles (NPs) were performed. These NPs were characterized and assessed for in vitro long-term monitoring of cell proliferation. Results: The optimization and validation of this method to track long-term cell proliferation assays have been achieved with high reproducibility, without cell cycle disruption. This method has been successfully applied in several adherent and suspension cells including hard-to-transfect cells and isolated human primary lymphocytes. Conclusion: A novel approach to track efficiently cellular proliferation by flow cytometry using fluorescence labeled NPs has been successfully developed. [GRAPHICS] .
引用
收藏
页码:1591 / 1605
页数:15
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