类有机物
细胞生物学
壁细胞
生物
胚胎干细胞
体外
肾脏发育
诱导多能干细胞
肾
祖细胞
解剖
干细胞
内皮干细胞
内分泌学
基因
生物化学
作者
Kimberly A. Homan,Navin Gupta,Katharina T. Kroll,David B. Kolesky,Mark A. Skylar‐Scott,Tomoya Miyoshi,Donald Mau,M. Todd Valerius,Thomas C. Ferrante,Joseph V. Bonventre,Jennifer A. Lewis,Ryuji Morizane
出处
期刊:Nature Methods
[Nature Portfolio]
日期:2019-02-11
卷期号:16 (3): 255-262
被引量:683
标识
DOI:10.1038/s41592-019-0325-y
摘要
Kidney organoids derived from human pluripotent stem cells have glomerular- and tubular-like compartments that are largely avascular and immature in static culture. Here we report an in vitro method for culturing kidney organoids under flow on millifluidic chips, which expands their endogenous pool of endothelial progenitor cells and generates vascular networks with perfusable lumens surrounded by mural cells. We found that vascularized kidney organoids cultured under flow had more mature podocyte and tubular compartments with enhanced cellular polarity and adult gene expression compared with that in static controls. Glomerular vascular development progressed through intermediate stages akin to those involved in the embryonic mammalian kidney's formation of capillary loops abutting foot processes. The association of vessels with these compartments was reduced after disruption of the endogenous VEGF gradient. The ability to induce substantial vascularization and morphological maturation of kidney organoids in vitro under flow opens new avenues for studies of kidney development, disease, and regeneration.
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