细胞外基质
体内
炎症
药理学
医学
癌症研究
细胞生物学
生物
免疫学
生物技术
作者
Jun Chen,Xixi Zhang,Robbie Cross,Yu-Jin Ahn,Gillian Huskin,Will Evans,Patrick T.J. Hwang,Jeong‐a Kim,Brigitta C. Brott,Hanjoong Jo,Young‐sup Yoon,Ho‐Wook Jun
出处
期刊:Biomaterials
[Elsevier]
日期:2023-12-27
卷期号:305: 122450-122450
标识
DOI:10.1016/j.biomaterials.2023.122450
摘要
In vitro atherosclerosis models are essential to evaluate therapeutics before in vivo and clinical studies, but significant limitations remain, such as the lack of three-layer vascular architecture and limited atherosclerotic features. Moreover, no scalable 3D atherosclerosis model is available for making high-throughput assays for therapeutic evaluation. Herein, we report an in vitro 3D three-layer nanomatrix vascular sheet with critical atherosclerosis multi-features (VSA), including endothelial dysfunction, monocyte recruitment, macrophages, extracellular matrix remodeling, smooth muscle cell phenotype transition, inflammatory cytokine secretion, foam cells, and calcification initiation. Notably, we present the creation of high-throughput functional assays with VSAs and the use of these assays for evaluating therapeutics for atherosclerosis treatment. The therapeutics include conventional drugs (statin and sirolimus), candidates for treating atherosclerosis (curcumin and colchicine), and potential gene therapy (miR-146a-loaded liposomes). The high efficiency and flexibility of the scalable VSA functional assays should facilitate drug discovery and development for atherosclerosis.
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