Garg K, Sell S A, Madurantakam P, Bowlin G L
Virginia Commonwealth University, Richmond, VA 23284, USA.
Biomed Mater. 2009 Jun;4(3):031001. doi: 10.1088/1748-6041/4/3/031001. Epub 2009 Apr 17.
The aim of this study was to investigate macrophage interactions with electrospun scaffolds and quantify the expression of key angiogenic growth factors in vitro. This study will further help in evaluating the potential of these electrospun constructs as vascular grafts for tissue repair and regeneration in situ. Human peripheral blood macrophages were seeded in serum free media on electrospun (10 mm) discs of polydioxanone (PDO), elastin and PDO:elastin blends (50:50, 70:30 and 90:10). The growth factor secretion was analyzed by ELISA. Macrophages produced high levels of vascular endothelial growth factor and acidic fibroblast growth factor. Transforming growth factor beta-1 (TGF-beta1) secretion was relatively low and there was negligible production of basic fibroblast growth factor. Therefore, it can be anticipated that these scaffolds will support tissue regeneration and angiogenesis.
本研究的目的是调查巨噬细胞与电纺支架的相互作用,并在体外定量关键血管生成生长因子的表达。本研究将进一步有助于评估这些电纺构建体作为原位组织修复和再生血管移植物的潜力。将人外周血巨噬细胞接种于无血清培养基中的聚二氧六环酮(PDO)、弹性蛋白以及PDO:弹性蛋白共混物(50:50、70:30和90:10)的电纺(10毫米)圆盘上。通过酶联免疫吸附测定法分析生长因子的分泌情况。巨噬细胞产生高水平的血管内皮生长因子和酸性成纤维细胞生长因子。转化生长因子β-1(TGF-β1)的分泌相对较低,碱性成纤维细胞生长因子的产生可忽略不计。因此,可以预期这些支架将支持组织再生和血管生成。