Engineering co-emergence in organoid models

被引:0
作者
Vasic, Ivana [1 ,2 ]
McDevitt, Todd C. [1 ,3 ]
机构
[1] Gladstone Inst, San Francisco, CA 94158 USA
[2] UC Berkeley UC San Francisco Grad Program Bioengn, San Francisco, CA USA
[3] Univ Calif San Francisco, Dept Bioengn & Therapeut Sci, San Francisco, CA 94143 USA
来源
PROGRESS IN BIOMEDICAL ENGINEERING | 2021年 / 3卷 / 02期
关键词
organoids; pluripotent stem cells; tissue engineering; symmetry breaking; morphogenesis; co-emergence; PLURIPOTENT STEM-CELLS; IN-VITRO EXPANSION; EXTRACELLULAR-MATRIX; SELF-ORGANIZATION; PROGENITOR CELLS; DIFFERENTIATION; CARDIOMYOCYTES; PRINCIPLES; CULTURE; BIOLOGY;
D O I
10.1088/2516-1091/abe41e
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Pluripotent stem cell-derived organoids provide in vitro models of development and disease that can be used for a wide range of biomedical applications, including high-throughput screens or regenerative medicine. The ability of stem cells to self-renew and self-organize in three dimensions is the basis for creating highly structured multicellular organoid models. However, progress in clinical translation of organoid technologies has been stymied by the stochastic nature of stem cell differentiation within organoids, which leads to inconsistent cell type maturity, tissue function, reproducibility, and control over macroscale structure and phenotype(s). Advances in our understanding of developmental biology and the mechanisms which regulate symmetry breaking and pattern formation in the embryo have led to new approaches for engineering cooperative emergence (co-emergence) in organoid models to address these challenges.
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页数:10
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