High-throughput deconvolution of 3D organoid dynamics at cellular resolution for cancer pharmacology with Cellos.
Patience MukashyakaPooja KumarDavid J MellertShadae NicholasJavad NoorbakhshMattia BrugioloElise T CourtoisOlga AnczukowEdison T LiuJeffrey H ChuangPublished in: Nature communications (2023)
Three-dimensional (3D) organoid cultures are flexible systems to interrogate cellular growth, morphology, multicellular spatial architecture, and cellular interactions in response to treatment. However, computational methods for analysis of 3D organoids with sufficiently high-throughput and cellular resolution are needed. Here we report Cellos, an accurate, high-throughput pipeline for 3D organoid segmentation using classical algorithms and nuclear segmentation using a trained Stardist-3D convolutional neural network. To evaluate Cellos, we analyze ~100,000 organoids with ~2.35 million cells from multiple treatment experiments. Cellos segments dye-stained or fluorescently-labeled nuclei and accurately distinguishes distinct labeled cell populations within organoids. Cellos can recapitulate traditional luminescence-based drug response of cells with complex drug sensitivities, while also quantifying changes in organoid and nuclear morphologies caused by treatment as well as cell-cell spatial relationships that reflect ecological affinity. Cellos provides powerful tools to perform high-throughput analysis for pharmacological testing and biological investigation of organoids based on 3D imaging.
Keyphrases
- high throughput
- single cell
- convolutional neural network
- deep learning
- cell therapy
- high resolution
- stem cells
- machine learning
- squamous cell carcinoma
- climate change
- cell death
- mesenchymal stem cells
- signaling pathway
- photodynamic therapy
- bone marrow
- young adults
- cell proliferation
- papillary thyroid
- drug induced
- fluorescence imaging
- high intensity
- childhood cancer