Direct On-Chip Differentiation of Intestinal Tubules from Induced Pluripotent Stem Cells

被引:59
作者
Naumovska, Elena [1 ,2 ]
Aalderink, Germaine [1 ]
Valencia, Christian Wong [2 ]
Kosim, Kinga [1 ,2 ]
Nicolas, Arnaud [1 ]
Brown, Stephen [2 ]
Vulto, Paul [1 ]
Erdmann, Kai S. [2 ]
Kurek, Dorota [1 ]
机构
[1] Mimetas BV, Model Dev, JH Oortweg 16, NL-2333 CH Leiden, Netherlands
[2] Univ Sheffield, Dept Biomed Sci, Sheffield S10 2TN, S Yorkshire, England
基金
欧盟地平线“2020”;
关键词
iPSC; intestinal organoids; directed differentiation; gut-on-a-chip; organ-on-a-chip; microfluidics; 3D cell culture; intestinal inflammation; IN-VITRO; DRUG DISCOVERY; ORGANOIDS; MODELS; IL-6; PREDICTION; CULTURE; CACO-2; TISSUE; NICHE;
D O I
10.3390/ijms21144964
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Intestinal organoids have emerged as the new paradigm for modelling the healthy and diseased intestine with patient-relevant properties. In this study, we show directed differentiation of induced pluripotent stem cells towards intestinal-like phenotype within a microfluidic device. iPSCs are cultured against a gel in microfluidic chips of the OrganoPlate, in which they undergo stepwise differentiation. Cells form a tubular structure, lose their stem cell markers and start expressing mature intestinal markers, including markers for Paneth cells, enterocytes and neuroendocrine cells. Tubes develop barrier properties as confirmed by transepithelial electrical resistance (TEER). Lastly, we show that tubules respond to pro-inflammatory cytokine triggers. The whole procedure for differentiation lasts 14 days, making it an efficient process to make patient-specific organoid tubules. We anticipate the usage of the platform for disease modelling and drug candidate screening.
引用
收藏
页码:1 / 15
页数:15
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