预处理内皮化移植物在大鼠肺动脉模型中减少狭窄和改善血管重塑。

IF 10.4 1区 医学 Q1 ENGINEERING, BIOMEDICAL
Acta Biomaterialia Pub Date : 2026-10-01 Epub Date: 2026-08-20 DOI:10.1016/j.actbio.2026.08.038
Wei Zhang, Qinzhe Xing, Séverine Ménoret, Ignacio Anegon, Yibing Qyang
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引用次数: 0

摘要

先天性心脏病的修复通常需要肺动脉重建,但目前的移植物选择仍然受到自体导管的缺乏和合成移植物耐久性差的限制,这些移植物经常因血栓形成、狭窄和钙化而失败。在低氧、低压的肺循环中,挑战会加剧。由于功能内皮对于预防血栓形成和新生内膜增生至关重要,我们设计了现成的内皮化组织工程血管移植物(TEVGs),采用逐步剪切预处理方案,模拟生理肺血流动力学。将人诱导多能干细胞来源的内皮细胞(iPSC-ECs)植入去细胞血管移植物,并在植入前进行脉动剪切应力调节。剪切预处理内皮化改善移植物顺应性,减少纤维蛋白原吸收,并增加内皮对体外缺氧应激的抵抗力。然后,我们在一个大鼠肺动脉移植模型中评估了移植物的性能,该模型旨在重现先天性心脏病的缺氧和狭窄易发环境。剪切预处理的内皮化移植物维持通畅一个月,支持宿主细胞再生,促进巨噬细胞介导的重塑,而所有对照移植物均出现严重狭窄。不通畅的移植物保留了肺泡结构,而狭窄的移植物导致肺渗出性损伤。这些研究结果表明,剪切预处理内皮化可能代表了一种产生功能性血管移植物用于肺动脉重建的策略,并建立了一个生理相关的小动物平台来评估TEVG在先天性心脏病中的表现。意义声明:有限的移植物可用性和缺乏功能性内皮层仍然是导致肺动脉重建中狭窄和移植物失败的关键因素。在这里,我们报道了一种内皮化组织工程血管移植物(TEVG)的发展,该血管移植物通过生理剪切应力预处理产生,以促进内皮成熟和对缺氧,低压肺环境的功能适应。为了评价移植体在生理相关条件下的性能,我们建立了可重复的大鼠左肺动脉移植模型。与发生严重狭窄的对照移植物相比,剪切预处理的内皮化TEVGs在植入后1个月保持管腔通畅并显示移植物再细胞化。这项工作提出了一种剪切预处理内皮化策略,以增强移植物的通畅和重塑,从而在生理相关的小动物模型中重建肺循环。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preconditioned endothelialized grafts reduce stenosis and improve vascular remodeling in a rat pulmonary artery model
Pulmonary artery reconstruction is frequently required for congenital heart disease repair, yet current graft options remain limited by the scarcity of autologous conduits and the poor durability of synthetic grafts, which often fail due to thrombosis, stenosis, and calcification. Challenges are exacerbated in the hypoxic, low-pressure pulmonary circulation. Because a functional endothelium is critical for preventing thrombosis and neointimal hyperplasia, we engineered ready-to-use endothelialized tissue-engineered vascular grafts (TEVGs) using a stepwise shear-preconditioning regimen that mimics physiological pulmonary hemodynamics. Human induced pluripotent stem cell-derived endothelial cells (iPSC-ECs) were seeded onto decellularized vascular grafts and conditioned under pulsatile shear stress before implantation. Shear-preconditioned endothelialization improved graft compliance, reduced fibrinogen absorption, and increased endothelial resistance to hypoxic stress in vitro. We then evaluated graft performance in a rat pulmonary artery transplantation model designed to recapitulate the hypoxic and stenosis-prone environment of congenital heart disease. Shear-preconditioned endothelialized grafts maintained patency for one month, supported host cell repopulation, and promoted macrophage-mediated remodeling, whereas all control grafts developed severe stenosis. Patent grafts preserved lung alveolar architecture, while stenotic grafts resulted in exudative lung injury. These findings suggest that shear-preconditioned endothelialization may represent a strategy to generate functional vascular grafts for pulmonary artery reconstruction and establish a physiologically relevant small-animal platform for evaluating TEVG performance in congenital heart diseases.

Statement of significance

Limited graft availability and the lack of functional endothelial layer remain key factors contributing to stenosis and graft failure in pulmonary artery reconstruction. Here, we reported development of an endothelialized tissue-engineered vascular graft (TEVG) generated through physiological shear-stress preconditioning to promote endothelial maturation and functional adaptation to the hypoxic, low-pressure pulmonary environment. To evaluate graft performance under physiologically relevant condition, we established a reproducible rat left pulmonary artery transplantation model. Compared with control grafts that developed severe stenosis, shear-preconditioned endothelialized TEVGs maintained luminal patency and showed graft recellularization at one month after implantation. This work presents a shear-preconditioned endothelialization strategy to enhance graft patency and remodeling for pulmonary circulation reconstruction in a physiologically relevant small animal model.
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来源期刊
Acta Biomaterialia
Acta Biomaterialia 工程技术-材料科学:生物材料
CiteScore
16.80
自引率
3.10%
发文量
776
审稿时长
30 days
期刊介绍: Acta Biomaterialia is a monthly peer-reviewed scientific journal published by Elsevier. The journal was established in January 2005. The editor-in-chief is W.R. Wagner (University of Pittsburgh). The journal covers research in biomaterials science, including the interrelationship of biomaterial structure and function from macroscale to nanoscale. Topical coverage includes biomedical and biocompatible materials.
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