| Literature DB >> 32726627 |
Shin-Ichi Mae1, Makoto Ryosaka1, Satoko Sakamoto2, Kyoko Matsuse1, Aya Nozaki1, Maiko Igami1, Ryotaro Kabai2, Akira Watanabe2, Kenji Osafune3.
Abstract
Ureteric bud (UB) is the embryonic kidney progenitor tissue that gives rise to the collecting duct and lower urinary tract. UB-like structures generated from human pluripotent stem cells by previously reported methods show limited developmental ability and limited branching. Here we report a method to generate UB organoids that possess epithelial polarity and tubular lumen and repeat branching morphogenesis. We also succeed in monitoring UB tip cells by utilizing the ability of tip cells to uptake very-low-density lipoprotein, cryopreserving UB progenitor cells, and expanding UB tip cells that can reconstitute the organoids and differentiate into collecting duct progenitors. Moreover, we successfully reproduce some phenotypes of multicystic dysplastic kidney (MCDK) using the UB organoids. These methods will help elucidate the developmental mechanisms of UB branching and develop a selective differentiation method for collecting duct cells, contributing to the creation of disease models for congenital renal abnormalities.Entities:
Keywords: branching; collecting duct; cryopreservation method; disease model; expansion culture; human induced pluripotent stem cell; monitoring method; tip cell; ureteric bud
Mesh:
Year: 2020 PMID: 32726627 DOI: 10.1016/j.celrep.2020.107963
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423