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首页> 外文期刊>Biomaterials Science >Polysaccharide electrospun fibers with sulfated poly(fucose) promote endothelial cell migration and VEGF-mediated angiogenesis
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Polysaccharide electrospun fibers with sulfated poly(fucose) promote endothelial cell migration and VEGF-mediated angiogenesis

机译:带有硫酸化聚岩藻糖的多糖电纺纤维可促进内皮细胞迁移和VEGF介导的血管生成

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Vascularization of tissue-engineered constructs is critical for proper cell and graft survival. In order to achieve this, pro-angiogenic factors, such as vascular endothelial growth factor (VEGF), are often incorporated into scaffolds by methods that either involve multiple steps or risk compromising protein bioactivity. In this study, we demonstrate a simple approach to incorporate VEGF into polysaccharide electrospun fibers by taking advantage of the interactions between VEGF and sulfated polysaccharide, fucoidan. Pullulan/dextran (P/D) electrospun fibers (diameter ~500 nm) incorporating fucoidan were fabricated by a one-step electrospinning process. Thereafter, VEGF was loaded onto the scaffolds. By varying the content of the chemical crosslinker, trisodium trimetaphosphate (STMP), from 10 to 12 and 16 wt% (denoted as STMP10, 12 and 16 respectively), the extent of fucoidan incorporation was significantly enhanced (<2.5 mg g~(-1) for STMP10 vs. 5 mg g~(-1) for STMP12 and 16). In addition, increased fucoidan content resulted in prolonged retention of VEGF bioactivity (≥14 days for STMP12 and 16 vs. 3 days for STMP10 and 1 day for VEGF by bolus delivery). Subcutaneous implantation of P/D scaffolds in mice demonstrated enhanced angiogenic response towards fucoidan and VEGF loaded scaffolds at 14 days post-implantation. In addition, P/D constructs supported rapid cellular infiltration and complete biodegradation of the scaffolds was observed at 7 days post-implantation. Taken together, the results demonstrate the potential of P/D electrospun fibers endowed with fucoidan as tunable reservoirs for the effective delivery of VEGF to control vascularization of tissue-engineered constructs.
机译:组织工程化构建体的血管化对于适当的细胞和移植物存活至关重要。为了实现这一点,促血管生成因子,例如血管内皮生长因子(VEGF),通常通过涉及多个步骤或冒着损害蛋白质生物活性风险的方法掺入支架中。在这项研究中,我们展示了一种简单的方法,可以利用VEGF与硫酸化多糖岩藻依聚糖之间的相互作用将VEGF掺入多糖电纺纤维中。采用一步法静电纺丝工艺制备了含岩藻依聚糖的支链淀粉/葡聚糖(P / D)电纺纤维(直径〜500 nm)。此后,将VEGF加载到支架上。通过将化学交联剂三偏磷酸三钠(STMP)的含量从10 wt%改变为12 wt%(分别表示为STMP10、12和16 wt%),岩藻依聚糖的掺入程度得到了显着提高(<2.5 mg g〜(- 1)对于STMP10,而对于STMP12和16,则为5 mg g(-1)。另外,岩藻依聚糖含量的增加导致VEGF生物活性的保留时间延长(通过推注递送,对于STMP12≥14天,对于STMP10≥16天,对于STMP10≥3天,对于VEGF≥1天)。在小鼠中皮下植入P / D支架表明,在植入后14天,对岩藻依聚糖和VEGF负载的支架的血管生成反应增强。另外,P / D构建体支持快速的细胞浸润,并且在植入后7天观察到支架的完全生物降解。两者合计,结果表明赋有岩藻依聚糖作为可调储库的P / D电纺纤维的潜力,可以有效地输送VEGF来控制组织工程构建体的血管生成。

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