A High-Throughput Automated Confocal Microscopy Platform for Quantitative Phenotyping of Nanoparticle Uptake and Transport in Spheroids

被引:30
|
作者
Cutrona, Meritxell B. [1 ,2 ,3 ]
Simpson, Jeremy C. [1 ,2 ,3 ]
机构
[1] UCD, Sch Biol & Environm Sci, Dublin D04 N2E5, Ireland
[2] UCD, Conway Inst Biomol & Biomed Res, Dublin D04 N2E5, Ireland
[3] Ctr Res Med Devices CURAM, Galway H91 W2TY, Ireland
基金
爱尔兰科学基金会;
关键词
high-content screening and analysis; membrane trafficking; nanoparticles; RAB GTPases; spheroids; INTRACELLULAR TRAFFICKING NETWORK; TUMOR SPHEROIDS; PENETRATION; ENDOCYTOSIS; EXOCYTOSIS; MODEL; ENHANCEMENT; EFFICACY; CULTURE; TARGETS;
D O I
10.1002/smll.201902033
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
There is a high demand for advanced, image-based, automated high-content screening (HCS) approaches to facilitate phenotypic screening in 3D cell culture models. A major challenge lies in retaining the resolution of fine cellular detail but at the same time imaging multicellular structures at a large scale. In this study, a confocal microscopy-based HCS platform in optical multiwell plates that enables the quantitative morphological profiling of populations of nonuniform spheroids obtained from HT-29 human colorectal cancer cells is described. This platform is then utilized to demonstrate a quantitative dissection of the penetration of synthetic nanoparticles (NP) in multicellular 3D spheroids at multiple levels of scale. A pilot RNA interference-based screening validates this methodology and identifies a subset of RAB GTPases that regulate NP trafficking in these spheroids. This technology is suitable for high-content phenotyping in 3D cell-based screening, providing a framework for nanomedicine drug development as applied to translational oncology.
引用
收藏
页数:14
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