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使用基于纳米技术的方法追踪细胞增殖。

Tracking cell proliferation using a nanotechnology-based approach.

作者信息

Altea-Manzano Patricia, Unciti-Broceta Juan Diego, Cano-Cortes Victoria, Ruiz-Blas María Paz, Valero-Griñan Teresa, Diaz-Mochon Juan Jose, Sanchez-Martin Rosario

机构信息

GENYO:Pfizer - Universidad de Granada-Junta de Andalucía Centre for Genomics & Oncological Research, Health Science Technological Park (PTS), Avenida de la Ilustración 114, 18016 Granada, Spain.

R&D Deparment, NanoGetic S. L. Granada HealthScienceTechnological Park (PTS), Avenida de la Innovación 1, Edificio BIC, 18016 Granada, Spain.

出版信息

Nanomedicine (Lond). 2017 Jul;12(13):1591-1605. doi: 10.2217/nnm-2017-0118. Epub 2017 May 17.

Abstract

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. [Formula: see text].

摘要

目的

开发一种基于纳米技术的高效荧光方法来追踪细胞增殖,以避免当前细胞标记染料的局限性。

材料与方法

对200纳米聚苯乙烯纳米颗粒(NPs)进行合成、聚乙二醇化、双功能化以及用荧光团(Cy5)标记。对这些纳米颗粒进行表征,并评估其用于细胞增殖的体外长期监测。

结果

该追踪长期细胞增殖试验方法已实现优化和验证,具有高重现性,且不会破坏细胞周期。此方法已成功应用于多种贴壁细胞和悬浮细胞,包括难以转染的细胞和分离的人原代淋巴细胞。

结论

已成功开发出一种通过使用荧光标记纳米颗粒的流式细胞术有效追踪细胞增殖的新方法。[公式:见正文]

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