3D multicellular systems in disease modelling: From organoids to organ-on-chip

被引:16
|
作者
Goldrick, Caoimhe [1 ]
Guri, Ina [1 ]
Herrera-Oropeza, Gabriel [1 ]
O'Brien-Gore, Charlotte [1 ]
Roy, Errin [1 ]
Wojtynska, Maja [1 ]
Spagnoli, Francesca M. [1 ]
机构
[1] Kings Coll London, Fac Life Sci, Ctr Gene Therapy & Regenerat Med, Guys Campus, London, England
基金
英国惠康基金;
关键词
organoids; assembloids; organ-on-chip; multicellular systems; disease modelling; HUMAN BRAIN-DEVELOPMENT; CELL-CULTURE; STEM-CELL; BASEMENT-MEMBRANE; MORPHOGENESIS; HYDROGELS; DIFFERENTIATION; MATRIX;
D O I
10.3389/fcell.2023.1083175
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cell-cell interactions underlay organ formation and function during homeostasis. Changes in communication between cells and their surrounding microenvironment are a feature of numerous human diseases, including metabolic disease and neurological disorders. In the past decade, cross-disciplinary research has been conducted to engineer novel synthetic multicellular organ systems in 3D, including organoids, assembloids, and organ-on-chip models. These model systems, composed of distinct cell types, satisfy the need for a better understanding of complex biological interactions and mechanisms underpinning diseases. In this review, we discuss the emerging field of building 3D multicellular systems and their application for modelling the cellular interactions at play in diseases. We report recent experimental and computational approaches for capturing cell-cell interactions as well as progress in bioengineering approaches for recapitulating these complexities ex vivo. Finally, we explore the value of developing such multicellular systems for modelling metabolic, intestinal, and neurological disorders as major examples of multisystemic diseases, we discuss the advantages and disadvantages of the different approaches and provide some recommendations for further advancing the field.
引用
收藏
页数:12
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