Automated 3D light-sheet screening with high spatiotemporal resolution reveals mitotic phenotypes.
Björn EismannTeresa G KriegerJürgen BenekeRuben BulkescherLukas AdamHolger ErfleCarl HerrmannRoland EilsChristian ConradPublished in: Journal of cell science (2020)
3D cell cultures enable the in vitro study of dynamic biological processes such as the cell cycle, but their use in high-throughput screens remains impractical with conventional fluorescent microscopy. Here, we present a screening workflow for the automated evaluation of mitotic phenotypes in 3D cell cultures by light-sheet microscopy. After sample preparation by a liquid handling robot, cell spheroids are imaged for 24 h in toto with a dual-view inverted selective plane illumination microscope (diSPIM) with a much improved signal-to-noise ratio, higher imaging speed, isotropic resolution and reduced light exposure compared to a spinning disc confocal microscope. A dedicated high-content image processing pipeline implements convolutional neural network-based phenotype classification. We illustrate the potential of our approach using siRNA knockdown and epigenetic modification of 28 mitotic target genes for assessing their phenotypic role in mitosis. By rendering light-sheet microscopy operational for high-throughput screening applications, this workflow enables target gene characterization or drug candidate evaluation in tissue-like 3D cell culture models.
Keyphrases
- high throughput
- cell cycle
- single cell
- deep learning
- single molecule
- high resolution
- convolutional neural network
- cell proliferation
- machine learning
- cell therapy
- genome wide
- optical coherence tomography
- mesenchymal stem cells
- high speed
- dna methylation
- label free
- emergency department
- drug delivery
- living cells
- genome wide identification
- risk assessment
- human health
- bioinformatics analysis