Zhu Zijin, Liu Zhirong, Zhang Donghui, Li Li, Pei Jianqiu, Cai Lin
State Key Laboratory of Biocatalysis and Enzyme Engineering, School of Life Science, National & Local Joint Engineering Research Center of High-Throughput Drug Screening Technology, Hubei University, Wuhan, 430062, China.
State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Cell Regen. 2024 Mar 1;13(1):6. doi: 10.1186/s13619-024-00189-8.
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.
钙化性主动脉瓣疾病(CAVD)在老年人中普遍存在,是最常见的心脏瓣膜病。目前,尚无药物干预措施能够有效逆转或预防CAVD,因此瓣膜置换成为主要的治疗手段。数十年来的广泛研究促成了动物和体外细胞模型的建立,这有助于更深入地了解CAVD的病理生理进展及潜在机制。在本综述中,我们全面总结并分析了常用于研究瓣膜钙化的模型的优缺点。我们特别强调了三维培养技术的进展,该技术可复制瓣膜的结构复杂性。此外,我们深入探讨了推进CAVD体内和体外模型研究的前瞻性建议。