Engineering Organ-on-a-Chip Systems for Vascular Diseases

被引:14
作者
Shakeri, Amid [1 ,4 ]
Wang, Ying [1 ,4 ]
Zhao, Yimu [1 ,4 ]
Landau, Shira [1 ,4 ]
Perera, Kevin [2 ]
Lee, Jonguk [1 ,5 ]
Radisic, Milica [1 ,3 ,4 ,6 ]
机构
[1] Univ Toronto, Inst Biomed Engn, Toronto, ON, Canada
[2] Univ Toronto, Dept Mech & Ind Engn, Toronto, ON, Canada
[3] Univ Toronto, Dept Chem Engn & Appl Chem, Toronto, ON, Canada
[4] Toronto Gen Res Inst, Toronto, ON, Canada
[5] Univ Hlth Network, KITE Toronto Rehabil Inst, Toronto, ON, Canada
[6] Univ Toronto, 164 Coll St,RS407, Toronto, ON M5S 3G9, Canada
基金
美国国家卫生研究院; 加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
endothelial cells; hemodynamics; microfluidics; microphysiological systems; vascular diseases; STEM-CELLS; THROMBOSIS; MODEL; BLOOD; FABRICATION; MIMICKING; CULTURE; MICROFLUIDICS; MECHANISMS; SCAFFOLD;
D O I
10.1161/ATVBAHA.123.318233
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Vascular diseases, such as atherosclerosis and thrombosis, are major causes of morbidity and mortality worldwide. Traditional in vitro models for studying vascular diseases have limitations, as they do not fully recapitulate the complexity of the in vivo microenvironment. Organ-on-a-chip systems have emerged as a promising approach for modeling vascular diseases by incorporating multiple cell types, mechanical and biochemical cues, and fluid flow in a microscale platform. This review provides an overview of recent advancements in engineering organ-on-a-chip systems for modeling vascular diseases, including the use of microfluidic channels, ECM (extracellular matrix) scaffolds, and patient-specific cells. We also discuss the limitations and future perspectives of organ-on-a-chip for modeling vascular diseases.
引用
收藏
页码:2241 / 2255
页数:15
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