|Publication Type||Journal Article|
|Year of Publication||2019|
|Authors||Subramanian, A, Sidhom, E-H, Emani, M, Vernon, K, Sahakian, N, Zhou, Y, Kost-Alimova, M, Slyper, M, Waldman, J, Dionne, D, Nguyen, LT, Weins, A, Marshall, JL, Rosenblatt-Rosen, O, Regev, A, Greka, A|
|Date Published||2019 11 29|
|Keywords||Animals, Cell Differentiation, Cell Line, Gene Expression Regulation, Developmental, Humans, Induced Pluripotent Stem Cells, Kidney, Kidney Transplantation, Mice, Organoids, Reproducibility of Results, Sequence Analysis, RNA, Single-Cell Analysis, Transplantation, Heterologous|
Human iPSC-derived kidney organoids have the potential to revolutionize discovery, but assessing their consistency and reproducibility across iPSC lines, and reducing the generation of off-target cells remain an open challenge. Here, we profile four human iPSC lines for a total of 450,118 single cells to show how organoid composition and development are comparable to human fetal and adult kidneys. Although cell classes are largely reproducible across time points, protocols, and replicates, we detect variability in cell proportions between different iPSC lines, largely due to off-target cells. To address this, we analyze organoids transplanted under the mouse kidney capsule and find diminished off-target cells. Our work shows how single cell RNA-seq (scRNA-seq) can score organoids for reproducibility, faithfulness and quality, that kidney organoids derived from different iPSC lines are comparable surrogates for human kidney, and that transplantation enhances their formation by diminishing off-target cells.
|Alternate Journal||Nat Commun|
|PubMed Central ID||PMC6884507|