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Label-free imaging of 3D pluripotent stem cell differentiation dynamics on chip.


ABSTRACT: Massive, parallelized 3D stem cell cultures for engineering in vitro human cell types require imaging methods with high time and spatial resolution to fully exploit technological advances in cell culture technologies. Here, we introduce a large-scale integrated microfluidic chip platform for automated 3D stem cell differentiation. To fully enable dynamic high-content imaging on the chip platform, we developed a label-free deep learning method called Bright2Nuc to predict in silico nuclear staining in 3D from confocal microscopy bright-field images. Bright2Nuc was trained and applied to hundreds of 3D human induced pluripotent stem cell cultures differentiating toward definitive endoderm on a microfluidic platform. Combined with existing image analysis tools, Bright2Nuc segmented individual nuclei from bright-field images, quantified their morphological properties, predicted stem cell differentiation state, and tracked the cells over time. Our methods are available in an open-source pipeline, enabling researchers to upscale image acquisition and phenotyping of 3D cell culture.

SUBMITTER: Atwell S 

PROVIDER: S-EPMC10391578 | biostudies-literature | 2023 Jul

REPOSITORIES: biostudies-literature

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Label-free imaging of 3D pluripotent stem cell differentiation dynamics on chip.

Atwell Scott S   Waibel Dominik Jens Elias DJE   Boushehri Sayedali Shetab SS   Wiedenmann Sandra S   Marr Carsten C   Meier Matthias M  

Cell reports methods 20230713 7


Massive, parallelized 3D stem cell cultures for engineering <i>in vitro</i> human cell types require imaging methods with high time and spatial resolution to fully exploit technological advances in cell culture technologies. Here, we introduce a large-scale integrated microfluidic chip platform for automated 3D stem cell differentiation. To fully enable dynamic high-content imaging on the chip platform, we developed a label-free deep learning method called Bright2Nuc to predict <i>in silico</i>  ...[more]

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