Journal article
Reporter-based fate mapping in human kidney organoids confirms nephron lineage relationships and reveals synchronous nephron formation
SE Howden, JM Vanslambrouck, SB Wilson, KS Tan, MH Little
EMBO Reports | WILEY | Published : 2019
Abstract
Nephron formation continues throughout kidney morphogenesis in both mice and humans. Lineage tracing studies in mice identified a self-renewing Six2-expressing nephron progenitor population able to give rise to the full complement of nephrons throughout kidney morphogenesis. To investigate the origin of nephrons within human pluripotent stem cell-derived kidney organoids, we performed a similar fate-mapping analysis of the SIX2-expressing lineage in induced pluripotent stem cell (iPSC)-derived kidney organoids to explore the feasibility of investigating lineage relationships in differentiating iPSCs in vitro. Using CRISPR/Cas9 gene-edited lineage reporter lines, we show that SIX2-expressing ..
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Awarded by National Institutes of Health
Funding Acknowledgements
The Murdoch Children's Research Institute is supported by the Victorian Government's Operational Infrastructure Support Program. The MCRI Gene Editing Facility is supported by the Stafford Fox Foundation. MHL is a Senior Principal Research Fellow of the National Health and Medical Research Council, Australia (GNT1136085). This work was supported by the National Institutes of Health, USA (DK107344-01), and the NHMRC (GNT1100970).