类有机物
诱导多能干细胞
细胞生物学
肾单位
肾
干细胞
中胚层
胚胎干细胞
生物
Wnt信号通路
成纤维细胞生长因子
输尿管芽
化学
解剖
肾脏发育
内分泌学
生物化学
信号转导
受体
基因
作者
Langping Gao,Yue J. Wang,Gang Wang,Hangdi Wu,Qingtao Yan,Jingjing Wang,Fei Liu,Haidong Fu,Wei Li,Lidan Hu,Jianhua Mao
摘要
Kidney organoids can be generated from induced pluripotent stem cells (iPSCs) through various approaches. These organoids hold great promise for disease modeling, drug screening, and potential therapeutic applications. This article presents a step-by-step procedure to create kidney organoids from iPSCs, starting from the posterior primitive streak (PS) to the intermediate mesoderm (IM). The approach relies on the APEL 2 medium, which is a defined, animal component-free medium. It is supplemented with a high concentration of WNT agonist (CHIR99021) for a duration of 4 days, followed by fibroblast growth factor 9 (FGF9)/heparin and a low concentration of CHIR99021 for an additional 3 days. During this process, emphasis is given to selecting the optimal cell density and CHIR99021 concentration at the start of iPSCs, as these factors are critical for successful kidney organoid generation. An important aspect of this protocol is the suspension culture in a low adherent plate, allowing the IM to gradually develop into nephron structures, encompassing glomerular, proximal tubular, and distal tubular structures, all presented in a visually comprehensible format. Overall, this detailed protocol offers an efficient and specific technique to produce kidney organoids from diverse iPSCs, ensuring successful and consistent results.
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