Models for calcific aortic valve disease in vivo and in vitro

被引:3
作者
Zhu, Zijin [1 ]
Liu, Zhirong [1 ]
Zhang, Donghui [1 ]
Li, Li [1 ]
Pei, Jianqiu [2 ,3 ]
Cai, Lin [1 ]
机构
[1] Hubei Univ, Natl & Local Joint Engn Res Ctr High Throughput Dr, Sch Life Sci, State Key Lab Biocatalysis & Enzyme Engn, Wuhan 430062, Peoples R China
[2] Chinese Acad Med Sci & Peking Union Med Coll, Fuwai Hosp, Natl Ctr Cardiovasc Dis, State Key Lab Cardiovasc Dis, Beijing, Peoples R China
[3] Capital Med Univ, Sch Basic Med Sci, Dept Biochem & Mol Biol, Beijing Key Lab Metab Disorders Related Cardiovasc, Beijing 100069, Peoples R China
基金
国家重点研发计划;
关键词
Calcific aortic valve disease; Animal model; In vitro; 3-dimentional culture; VALVULAR INTERSTITIAL CELL; GROWTH-FACTOR; RABBIT MODEL; STEM-CELLS; STENOSIS; RECEPTOR; HYPERCHOLESTEROLEMIA; DIFFERENTIATION; INFLAMMATION; PROGRESSION;
D O I
10.1186/s13619-024-00189-8
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Calcific Aortic Valve Disease (CAVD) is prevalent among the elderly as the most common valvular heart disease. Currently, no pharmaceutical interventions can effectively reverse or prevent CAVD, making valve replacement the primary therapeutic recourse. Extensive research spanning decades has contributed to the establishment of animal and in vitro cell models, which facilitates a deeper understanding of the pathophysiological progression and underlying mechanisms of CAVD. In this review, we provide a comprehensive summary and analysis of the strengths and limitations associated with commonly employed models for the study of valve calcification. We specifically emphasize the advancements in three-dimensional culture technologies, which replicate the structural complexity of the valve. Furthermore, we delve into prospective recommendations for advancing in vivo and in vitro model studies of CAVD.
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页数:16
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