A Modular Differentiation System Maps Multiple Human Kidney Lineages from Pluripotent Stem Cells

Hiraku Tsujimoto(Kyoto University), Tomoko Kasahara(Kyoto University), Shinichi Sueta(Kyoto University), Toshikazu Araoka(Kyoto University), Satoko Sakamoto(Kyoto University), Chihiro Okada(Kyoto University), Shin-Ichi Mae(Kyoto University), Taiki Nakajima(Kyoto University), Natsumi Okamoto(Kyoto University), Daisuke Taura(Kyoto University), Makoto Nasu(Kyoto University), Tatsuya Shimizu(Kyoto University), Makoto Ryosaka(Kyoto University), Zhongwei Li(University of Southern California), Masakatsu Sone(Kyoto University), Makoto Ikeya(Kyoto University), Akira Watanabe(Kyoto University), Kenji Osafune(Kyoto University)
Cell Reports
April 1, 2020
Cited by 109Open Access
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Abstract

Recent studies using human pluripotent stem cells (hPSCs) have developed protocols to induce kidney-lineage cells and reconstruct kidney organoids. However, the separate generation of metanephric nephron progenitors (NPs), mesonephric NPs, and ureteric bud (UB) cells, which constitute embryonic kidneys, in in vitro differentiation culture systems has not been fully investigated. Here, we create a culture system in which these mesoderm-like cell types and paraxial and lateral plate mesoderm-like cells are separately generated from hPSCs. We recapitulate nephrogenic niches from separately induced metanephric NP-like and UB-like cells, which are subsequently differentiated into glomeruli, renal tubules, and collecting ducts in vitro and further vascularized in vivo. Our selective differentiation protocols should contribute to understanding the mechanisms underlying human kidney development and disease and also supply cell sources for regenerative therapies.


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