诱导多能干细胞
祖细胞
干细胞
祖细胞
小岛
细胞生物学
细胞分化
β细胞
生物
定向微分
胰岛素
内分泌学
胚胎干细胞
遗传学
基因
作者
Jia Zhao,Shenghui Liang,Mitchell J.S. Braam,Robert K. Baker,Diepiriye G. Iworima,Nina Quiskamp,Timothy J. Kieffer
摘要
Differentiation of human pluripotent stem cells (hPSCs) into insulin-secreting beta cells provides material for investigating beta cell function and diabetes treatment. However, challenges remain in obtaining stem cell-derived beta cells that adequately mimic native human beta cells. Building upon previous studies, hPSC-derived islet cells have been generated to create a protocol with improved differentiation outcomes and consistency. The protocol described here utilizes a pancreatic progenitor kit during Stages 1-4, followed by a protocol modified from a paper previously published in 2014 (termed "R-protocol" hereafter) during Stages 5-7. Detailed procedures for using the pancreatic progenitor kit and 400 µm diameter microwell plates to generate pancreatic progenitor clusters, R-protocol for endocrine differentiation in a 96-well static suspension format, and in vitro characterization and functional evaluation of hPSC-derived islets, are included. The complete protocol takes 1 week for initial hPSC expansion followed by ~5 weeks to obtain insulin-producing hPSC islets. Personnel with basic stem cell culture techniques and training in biological assays can reproduce this protocol.
科研通智能强力驱动
Strongly Powered by AbleSci AI