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Advanced lung organoids for respiratory system and pulmonary disease modeling
被引:5
|作者:
Joo, Hyebin
[1
]
Min, Sungjin
[1
]
Cho, Seung-Woo
[1
,2
,3
]
机构:
[1] Yonsei Univ, Dept Biotechnol, Seoul, South Korea
[2] Inst Basic Sci IBS, Ctr Nanomed, Seoul, South Korea
[3] Yonsei Univ, Dept Biotechnol, 50 Yonsei Ro, Seoul 03722, South Korea
基金:
新加坡国家研究基金会;
关键词:
Lung organoid;
bioengineeing platform;
cellular niches;
respiratory infection;
pulmonary fibrosis;
STEM-CELLS;
CYSTIC-FIBROSIS;
EXTRACELLULAR-MATRIX;
MECHANICAL-TENSION;
AIRWAY EPITHELIUM;
BASAL-CELLS;
GENERATION;
HYDROGELS;
TRACHEA;
CULTURE;
D O I:
10.1177/20417314241232502
中图分类号:
Q813 [细胞工程];
学科分类号:
摘要:
Amidst the recent coronavirus disease 2019 (COVID-19) pandemic, respiratory system research has made remarkable progress, particularly focusing on infectious diseases. Lung organoid, a miniaturized structure recapitulating lung tissue, has gained global attention because of its advantages over other conventional models such as two-dimensional (2D) cell models and animal models. Nevertheless, lung organoids still face limitations concerning heterogeneity, complexity, and maturity compared to the native lung tissue. To address these limitations, researchers have employed co-culture methods with various cell types including endothelial cells, mesenchymal cells, and immune cells, and incorporated bioengineering platforms such as air-liquid interfaces, microfluidic chips, and functional hydrogels. These advancements have facilitated applications of lung organoids to studies of pulmonary diseases, providing insights into disease mechanisms and potential treatments. This review introduces recent progress in the production methods of lung organoids, strategies for improving maturity, functionality, and complexity of organoids, and their application in disease modeling, including respiratory infection and pulmonary fibrosis.
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页数:24
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