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纤维蛋白凝胶固定的血管内皮生长因子和碱性成纤维细胞生长因子在动静脉环模型中能有效刺激血管生成。

Fibrin gel-immobilized VEGF and bFGF efficiently stimulate angiogenesis in the AV loop model.

作者信息

Arkudas Andreas, Tjiawi Jimmy, Bleiziffer Oliver, Grabinger Lucia, Polykandriotis Elias, Beier Justus P, Stürzl Michael, Horch Raymund E, Kneser Ulrich

机构信息

Department of Plastic and Hand Surgery, University of Erlangen Medical Center, Erlangen, Germany.

出版信息

Mol Med. 2007 Sep-Oct;13(9-10):480-7. doi: 10.2119/2007-00057.Arkudas.

Abstract

The modulation of angiogenic processes in matrices is of great interest in tissue engineering. We assessed the angiogenic effects of fibrin-immobilized VEGF and bFGF in an arteriovenous loop (AVL) model in 22 AVLs created between the femoral artery and vein in rats. The loops were placed in isolation chambers and were embedded in 500 microL fibrin gel (FG) (group A) or in 500 microL FG loaded with 0.1 ng/microL VEGF and 0.1 ng/microL bFGF (group B). After two and four weeks specimens were explanted and investigated using histological, morphometrical, and ultramorphological [scanning electron microscope (SEM) of vascular corrosion replicas] techniques. In both groups, the AVL induced formation of densely vascularized connective tissue with differentiated and functional vessels inside the fibrin matrix. VEGF and bFGF induced significantly higher absolute and relative vascular density and a faster resorption of the fibrin matrix. SEM analysis in both groups revealed characteristics of an immature vascular bed, with a higher vascular density in group B. VEGF and bFGF efficiently stimulated sprouting of blood vessels in the AVL model. The implantation of vascular carriers into given growth factor-loaded matrix volumes may eventually allow efficient generation of axially vascularized, tissue-engineered composites.

摘要

基质中血管生成过程的调控在组织工程领域备受关注。我们在大鼠股动脉和静脉之间构建的22个动静脉环(AVL)模型中,评估了纤维蛋白固定化血管内皮生长因子(VEGF)和碱性成纤维细胞生长因子(bFGF)的血管生成作用。将这些动静脉环置于隔离室中,分别嵌入500微升纤维蛋白凝胶(FG)(A组)或含有0.1纳克/微升VEGF和0.1纳克/微升bFGF的500微升FG中(B组)。两周和四周后取出标本,采用组织学、形态计量学和超微形态学[血管铸型扫描电子显微镜(SEM)]技术进行研究。在两组中,动静脉环均诱导纤维蛋白基质内形成血管密集的结缔组织,其中含有分化且功能正常的血管。VEGF和bFGF诱导的绝对和相对血管密度显著更高,且纤维蛋白基质的吸收更快。两组的SEM分析均显示出不成熟血管床的特征,B组的血管密度更高。VEGF和bFGF在AVL模型中有效刺激了血管的芽生。将血管载体植入给定生长因子负载的基质体积中,最终可能实现轴向血管化组织工程复合材料的高效生成。

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