Generation of nephron progenitor cells and kidney organoids from human pluripotent stem cells

被引:139
|
作者
Morizane, Ryuji [1 ,2 ,3 ]
Bonventre, Joseph V. [1 ,2 ,3 ]
机构
[1] Brigham & Womens Hosp, Renal Div, 75 Francis St, Boston, MA 02115 USA
[2] Harvard Med Sch, Dept Med, Boston, MA 02215 USA
[3] Harvard Stem Cell Inst, Cambridge, MA 02138 USA
基金
美国国家卫生研究院;
关键词
INTERMEDIATE MESODERM; IN-VIVO; DIFFERENTIATION; DISEASE; INJURY; MODEL; ACTIVATION; MOLECULE-1; INDUCTION; BIOMARKER;
D O I
10.1038/nprot.2016.170
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A variety of protocols have been developed that demonstrate the capability to differentiate human pluripotent stem cells (hPSCs) into kidney structures. Our goal was to develop a high-efficiency protocol to generate nephron progenitor cells (NPCs) and kidney organoids to facilitate applications for tissue engineering, disease modeling and chemical screening. Here, we describe a detailed protocol resulting in high-efficiency production (80-90%) of NPCs from hPSCs within 9 d of differentiation. Kidney organoids were generated from NPCs within 12 d with high reproducibility using 96-well plates suitable for chemical screening. The protocol requires skills for culturing hPSCs and careful attention to morphological changes indicative of differentiation. This kidney organoid system provides a platform for studies of human kidney development, modeling of kidney diseases, nephrotoxicity and kidney regeneration. The system provides a model for in vitro study of kidney intracellular and intercompartmental interactions using differentiated human cells in an appropriate nephron and stromal context.
引用
收藏
页码:195 / 207
页数:13
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