A Small-Diameter Artificial Vascular Graft: Biocompatibility Evaluation and Regulatory Mechanisms of Vascular Remodeling at the Cellular and Molecular Levels

生物相容性 血管移植 血管壁 细胞生物学 化学 生物医学工程 医学 生物 内科学 有机化学
作者
Zhenhao Zhang,Shuo Wang,Jiafei Li,Gang Tian,Ting Pan,Yunhui Lv,Matthew Yung,Peng Peng,Xuemin Wang,Xiaodong Hao,Qi Zhang,Jiafei Luo,Xue Zhang,Peihe Wang,J. H. Fan,Chen‐Yang Shen,Jinyan Zhu,Yongchun Cui
出处
期刊:ACS applied bio materials [American Chemical Society]
卷期号:8 (9): 7925-7941 被引量:1
标识
DOI:10.1021/acsabm.5c00942
摘要

The increasing prevalence of cardiovascular diseases highlights the urgent demand for small-diameter artificial vascular grafts (SD-AVGs). However, the clinical application of current SD-AVGs is limited by complications such as thrombosis and proliferative stenosis. We first designed and fabricated a triple-layered SD-AVG (TL-SD-AVG) composed of polycarbonate polyurethane and polyethylene terephthalate using electrospinning and mixed weaving techniques. Then, we characterized its mechanical properties through standard mechanical testing. Cytotoxicity, cell adhesion assay hemolysis, and blood clotting assays were subsequently performed to preliminarily evaluate its cytocompatibility and hemocompatibility in vitro. Next, we assessed the TL-SD-AVG's tissue compatibility and biosafety using a porcine carotid artery replacement model. Finally, we employed both bulk RNA sequencing (RNA-seq) and single-nucleus RNA sequencing (snRNA-seq) to investigate the cellular and molecular mechanisms involved in vascular remodeling. Our results showed that the TL-SD-AVG exhibited adequate mechanical strength, low cytotoxicity, and a hemolysis rate below 5%, and its anticoagulant performance was better than the expanded polytetrafluoroethylene control graft. In vivo, the grafts maintained structural integrity and patency over a 4-week period, with no thrombus formation or pathological stenosis. Histopathological analyses revealed endothelial coverage of 34.66 ± 4.47% at 1 week, increasing to 72.14 ± 4.01% by 4 weeks. RNA-seq and snRNA-seq identified six key cell types involved in vascular regeneration, with no significant aberrations in pathways related to vascular remodeling. Both in vitro and in vivo experiments demonstrated that TL-SD-AVG had low cytotoxicity, good hemocompatibility, favorable histocompatibility, and overall biosafety. Moreover, it supported effective vascular remodeling, providing a robust theoretical and experimental foundation for its future clinical translation.
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