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通过优化动态条件培养实现自体纤维蛋白基组织工程心脏瓣膜的体外发育

The in vitro development of autologous fibrin-based tissue-engineered heart valves through optimised dynamic conditioning.

作者信息

Flanagan Thomas C, Cornelissen Christian, Koch Sabine, Tschoeke Beate, Sachweh Joerg S, Schmitz-Rode Thomas, Jockenhoevel Stefan

机构信息

Cardiovascular Tissue Engineering Group, Department of Applied Medical Engineering, Helmholtz Institute for Biomedical Engineering, RWTH Aachen University, Pauwelsstrasse 20, 52074 Aachen, Germany.

出版信息

Biomaterials. 2007 Aug;28(23):3388-97. doi: 10.1016/j.biomaterials.2007.04.012. Epub 2007 Apr 13.

Abstract

Our group has previously demonstrated the synthesis of a completely autologous fibrin-based heart valve structure using the principles of tissue engineering. The present approach aims to guide more mature tissue development in fibrin-based valves based on in vitro conditioning in a custom-designed bioreactor system. Moulded fibrin-based tissue-engineered heart valves seeded with ovine carotid artery-derived cells were subjected to 12 days of mechanical conditioning in a bioreactor system. The bioreactor pulse rate was increased from 5 to 10 b.p.m. after 6 days, while a pressure difference of 20 mmH(2)O was maintained over the valve leaflets. Control valves were cultured under stirred conditions in a beaker. Cell phenotype and extracellular matrix (ECM) composition were analysed in all samples and compared to native ovine aortic valve tissue using routine histological and immunohistochemical techniques. Conditioned valve leaflets showed reduced tissue shrinkage compared to stirred controls. Limited ECM synthesis was evident in stirred controls, while the majority of cells were detached from the fibrin scaffold. Dynamic conditioning increased cell attachment/alignment and expression of alpha-smooth muscle actin, while enhancing the deposition of ECM proteins, including types I and III collagen, fibronectin, laminin and chondroitin sulphate. There was no evidence for elastin synthesis in either stirred controls or conditioned samples. The present study demonstrates that the application of low-pressure conditions and increasing pulsatile flow not only enhances seeded cell attachment and alignment within fibrin-based heart valves, but dramatically changes the manner in which these cells generate ECM proteins and remodel the valve matrix. Optimised dynamic conditioning, therefore, might accelerate the maturation of surgically feasible and implantable autologous fibrin-based tissue-engineered heart valves.

摘要

我们的团队此前已证明,利用组织工程原理可合成完全自体的纤维蛋白基心脏瓣膜结构。目前的方法旨在基于在定制设计的生物反应器系统中进行体外预处理,引导纤维蛋白基瓣膜中更成熟的组织发育。将接种了绵羊颈动脉来源细胞的模制纤维蛋白基组织工程心脏瓣膜在生物反应器系统中进行12天的机械预处理。6天后,生物反应器的脉搏率从5次/分钟增加到10次/分钟,同时在瓣膜小叶上维持20 mmHg₂O的压差。对照瓣膜在烧杯中搅拌条件下培养。使用常规组织学和免疫组织化学技术分析所有样本中的细胞表型和细胞外基质(ECM)组成,并与天然绵羊主动脉瓣膜组织进行比较。与搅拌对照相比,预处理后的瓣膜小叶组织收缩减少。在搅拌对照中,ECM合成有限,而大多数细胞从纤维蛋白支架上脱落。动态预处理增加了细胞附着/排列以及α-平滑肌肌动蛋白的表达,同时增强了ECM蛋白的沉积,包括I型和III型胶原、纤连蛋白、层粘连蛋白和硫酸软骨素。在搅拌对照或预处理样本中均未发现弹性蛋白合成的证据。本研究表明,施加低压条件和增加脉动流不仅能增强接种细胞在纤维蛋白基心脏瓣膜内的附着和排列,还能显著改变这些细胞产生ECM蛋白和重塑瓣膜基质的方式。因此,优化的动态预处理可能会加速手术可行且可植入的自体纤维蛋白基组织工程心脏瓣膜的成熟。

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