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Parallel generation of easily selectable multiple nephronal cell types from human pluripotent stem cells.

Item Type:Article
Title:Parallel generation of easily selectable multiple nephronal cell types from human pluripotent stem cells.
Creators Name:Hariharan, K. and Stachelscheid, H. and Rossbach, B. and Oh, S.J. and Mah, N. and Schmidt-Ott, K. and Kurtz, A. and Reinke, P.
Abstract:Human pluripotent stem cells (hPSCs) provide a source for the generation of defined kidney cells and renal organoids applicable in regenerative medicine, disease modeling, and drug screening. These applications require the provision of hPSC-derived renal cells by reproducible, scalable, and efficient methods. We established a chemically defined protocol by application of Activin A, BMP4, and Retinoic acid followed by GDNF, which steered hPSCs to the renal lineage and resulted in populations of SIX2(+)/CITED1(+) metanephric mesenchyme- (MM) and of HOXB7(+)/GRHL2(+) ureteric bud (UB)-like cells already by 6 days. Transcriptome analysis corroborated that the PSC-derived cell types at day 8 resemble their renal vesicle and ureteric epithelial counterpart in vivo, forming tubular and glomerular renal cells 6 days later. We demonstrate that starting from hPSCs, our in vitro protocol generates a pool of nephrogenic progenitors at the renal vesicle stage, which can be further directed into specialized nephronal cell types including mesangial-, proximal tubular-, distal tubular, collecting duct epithelial cells, and podocyte precursors after 14 days. This simple and rapid method to produce renal cells from a common precursor pool in 2D culture provides the basis for scaled-up production of tailored renal cell types, which are applicable for drug testing or cell-based regenerative therapies.
Keywords:HPSCS, Renal Progenitors, Differentiation, Tubules, Renal Vesicle, Nephron, Animals
Source:Cellular and Molecular Life Sciences
ISSN:1420-682X
Publisher:Springer (Switzerland)
Volume:76
Number:1
Page Range:179
Date:January 2019
Official Publication:https://doi.org/10.1007/s00018-018-2929-2
PubMed:View item in PubMed

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