Skip to Content
Merck
  • A Modular Differentiation System Maps Multiple Human Kidney Lineages from Pluripotent Stem Cells.

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

Cell reports (2020-04-09)
Hiraku Tsujimoto, Tomoko Kasahara, Shin-Ichi Sueta, Toshikazu Araoka, Satoko Sakamoto, Chihiro Okada, Shin-Ichi Mae, Taiki Nakajima, Natsumi Okamoto, Daisuke Taura, Makoto Nasu, Tatsuya Shimizu, Makoto Ryosaka, Zhongwei Li, Masakatsu Sone, Makoto Ikeya, Akira Watanabe, Kenji Osafune
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.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
TTNPB
Sigma-Aldrich
Anti-HNF1B antibody produced in rabbit, Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution
Sigma-Aldrich
Retinoic acid, ≥98% (HPLC), powder
Sigma-Aldrich
IWR-1, ≥98% (HPLC)
Sigma-Aldrich
DAPT, ≥98% (HPLC), solid
Sigma-Aldrich
Monoclonal Anti-Calbindin-D-28K antibody produced in mouse, clone CB-955, ascites fluid