再狭窄
血管平滑肌
内膜增生
新生内膜增生
支架
药品
医学
药物洗脱支架
平滑肌
生物医学工程
癌症研究
药理学
内科学
作者
Haoshuang Wu,Li Yang,Rifang Luo,Li Li,Tiantian Zheng,Kaiyang Huang,Yumei Qin,Xia Yang,Qian Zhang,Yunbing Wang
标识
DOI:10.1038/s41467-024-44902-2
摘要
Abstract Drug-eluting stent implantation suppresses the excessive proliferation of smooth muscle cells to reduce in-stent restenosis. However, the efficacy of drug-eluting stents remains limited due to delayed reendothelialization, impaired intimal remodeling, and potentially increased late restenosis. Here, we show that a drug-free coating formulation functionalized with tailored recombinant humanized type III collagen exerts one-produces-multi effects in response to injured tissue following stent implantation. We demonstrate that the one-produces-multi coating possesses anticoagulation, anti-inflammatory, and intimal hyperplasia suppression properties. We perform transcriptome analysis to indicate that the drug-free coating favors the endothelialization process and induces the conversion of smooth muscle cells to a contractile phenotype. We find that compared to drug-eluting stents, our drug-free stent reduces in-stent restenosis in rabbit and porcine models and improves vascular neointimal healing in a rabbit model. Collectively, the one-produces-multi drug-free system represents a promising strategy for the next-generation of stents.
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