Differentiation and CRISPR-Cas9-mediated genetic engineering of human intestinal organoids

被引:4
|
作者
Martinez-Silgado, Adriana [1 ,2 ]
Yengej, Fjodor A. Yousef [1 ,2 ,3 ]
Puschhof, Jens [1 ,2 ,4 ]
Geurts, Veerle [1 ,2 ]
Boot, Charelle [1 ,2 ]
Geurts, Maarten H. [1 ,2 ]
Rookmaaker, Maarten B. [3 ]
Verhaar, Marianne C.
Beumer, Joep [1 ,2 ]
Clevers, Hans [1 ,2 ,5 ]
机构
[1] Hubrecht Inst, Royal Netherlands Acad Arts & Sci KNAW, Oncode Inst, NL-3584 CT Utrecht, Netherlands
[2] UMC Utrecht, NL-3584 CT Utrecht, Netherlands
[3] Univ Med Ctr Utrecht, Dept Nephrol & Hypertens, NL-3584 CX Utrecht, Netherlands
[4] German Canc Res Ctr, Microbiome & Canc Div, Neuenheimer Feld 280, D-69120 Heidelberg, Germany
[5] F Hoffmann La Roche Ltd, Pharma Res & Early Dev pRED, Basel, Switzerland
来源
STAR PROTOCOLS | 2022年 / 3卷 / 03期
基金
欧洲研究理事会;
关键词
STEM-CELLS; IN-VITRO;
D O I
10.1016/j.xpro.2022.101639
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Intestinal organoids are three-dimensional cultures that resemble key aspects of the epithelium of origin. Here, we describe how to differentiate human small intestinal organoids by combining growth media variations and genetic engineering. We detail the differentiation of human intestinal organoids in the presence and absence of BMP agonists to recapitulate a broader scope of functional cell states found in vivo. Using transient overexpression of the transcription factor Neurogenin-3, we describe the enhancement of differentiation toward rare enteroendocrine cells.For complete details on the use and execution of this protocol, please refer to Beumer et al. (2022).
引用
收藏
页数:23
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