CelltypeR: A flow cytometry pipeline to characterize single cells from brain organoids.
Rhalena A ThomasJulien SiroisShuming LiAlexandre GestinGhislaine DeyabValerio E C PiscopoPaula LépineMeghna MathurCarol X-Q ChenVincent SoubannierTaylor M GoldsmithLama FawazThomas M DurcanEdward A FonPublished in: iScience (2024)
Motivated by the cellular heterogeneity in complex tissues, particularly in brain and induced pluripotent stem cell (iPSC)-derived brain models, we developed a complete workflow to reproducibly characterize cell types in complex tissues. Our approach combines a flow cytometry (FC) antibody panel with our computational pipeline CelltypeR, enabling dataset aligning, unsupervised clustering optimization, cell type annotating, and statistical comparisons. Applied to human iPSC derived midbrain organoids, it successfully identified the major brain cell types. We performed fluorescence-activated cell sorting of CelltypeR-defined astrocytes, radial glia, and neurons, exploring transcriptional states by single-cell RNA sequencing. Among the sorted neurons, we identified subgroups of dopamine neurons: one reminiscent of substantia nigra cells most vulnerable in Parkinson's disease. Finally, we used our workflow to track cell types across a time course of organoid differentiation. Overall, our adaptable analysis framework provides a generalizable method for reproducibly identifying cell types across FC datasets in complex tissues.
Keyphrases
- single cell
- rna seq
- flow cytometry
- stem cells
- cell therapy
- high throughput
- resting state
- gene expression
- white matter
- spinal cord
- endothelial cells
- functional connectivity
- transcription factor
- blood brain barrier
- spinal cord injury
- multiple sclerosis
- electronic health record
- subarachnoid hemorrhage
- high glucose
- cell cycle arrest
- pi k akt
- data analysis