Organoid-Derived Epithelial Monolayer: A Clinically Relevant In Vitro Model for Intestinal Barrier Function

被引:11
|
作者
van Dooremalen, Wies T. M. [1 ]
Derksen, Merel [1 ]
Roos, Jamie Lee [1 ]
Baron, Celia Higuera [1 ]
Verissimo, Carla S. [1 ]
Vries, Robert G. J. [1 ]
Boj, Sylvia F. [1 ]
Pourfarzad, Farzin [1 ]
机构
[1] Fdn Hubrecht Organoid Technol HUB, Utrecht, Netherlands
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2021年 / 173期
关键词
STEM-CELLS; PROGENITOR CELLS; TEER MEASUREMENT; EXPANSION; BIOBANK; LGR5;
D O I
10.3791/62074
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In the past, intestinal epithelial model systems were limited to transformed cell lines and primary tissue. These model systems have inherent limitations as the former do not faithfully represent original tissue physiology, and the availability of the latter is limited. Hence, their application hampers fundamental and drug development research. Adult stem-cell-based organoids (henceforth referred to as organoids) are miniatures of normal or diseased epithelial tissue from which they are derived. They can be established very efficiently from different gastrointestinal (GI) tract regions, have long-term expandability, and simulate tissue- and patient-specific responses to treatments in vitro. Here, the establishment of intestinal organoid-derived epithelial monolayers has been demonstrated along with methods to measure epithelial barrier integrity, permeability and transport, antimicrobial protein secretion, as well as histology. Moreover, intestinal organoid-derived monolayers can be enriched with proliferating stem and transit-amplifying cells as well as with key differentiated epithelial cells. Therefore, they represent a model system that can be tailored to study the effects of compounds on target cells and their mode of action. Although organoid cultures are technically more demanding than cell lines, once established, they can reduce failures in the later stages of drug development as they truly represent in vivo epithelium complexity and interpatient heterogeneity.
引用
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页数:22
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