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首页> 外文期刊>Biomaterials >Effect of local sequential VEGF and BMP-2 delivery on ectopic and orthotopic bone regeneration.
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Effect of local sequential VEGF and BMP-2 delivery on ectopic and orthotopic bone regeneration.

机译:局部顺序VEGF和BMP-2递送对异位和原位骨再生的影响。

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Bone regeneration is a coordinated cascade of events regulated by several cytokines and growth factors. Angiogenic growth factors are predominantly expressed during the early phases for re-establishment of the vascularity, whereas osteogenic growth factors are continuously expressed during bone formation and remodeling. Since vascular endothelial growth factor (VEGF) and bone morphogenetic proteins (BMPs) are key regulators of angiogenesis and osteogenesis during bone regeneration, the aim of this study was to investigate if their sequential release could enhance BMP-2-induced bone formation. A composite consisting of poly(lactic-co-glycolic acid) microspheres loaded with BMP-2 embedded in a poly(propylene) scaffold surrounded by a gelatin hydrogel loaded with VEGF was used for the sequential release of the growth factors. Empty composites or composites loaded with VEGF and/or BMP-2 were implanted ectopically and orthotopically in Sprague-Dawley rats (n=9). Following implantation, the local release profiles were determined by measuring the activity of (125)I-labeled growth factors using scintillation probes. After 8 weeks blood vessel and bone formation were analyzed using microangiography, microCT and histology. The scaffolds exhibited a large initial burst release of VEGF within the first 3 days and a sustained release of BMP-2 over the full 56-day implantation period. Although VEGF did not induce bone formation, it did increase the formation of the supportive vascular network (p=0.03) in ectopic implants. In combination with local sustained BMP-2 release, VEGF significantly enhanced ectopic bone formation compared to BMP-2 alone (p=0.008). In the orthotopic defects, no effect of VEGF on vascularisation was found, nor was bone formation higher by the combination of growth factors, compared to BMP-2 alone. This study demonstrates that a sequential angiogenic and osteogenic growth factor release may be beneficial for the enhancement of bone regeneration.
机译:骨再生是由几种细胞因子和生长因子调节的事件的协调级联。血管生成生长因子主要在重建血管的早期阶段表达,而成骨生长因子在骨骼形成和重塑过程中持续表达。由于血管内皮生长因子(VEGF)和骨形态发生蛋白(BMP)是骨骼再生过程中血管生成和成骨的关键调节剂,因此本研究的目的是研究它们的顺序释放是否可以增强BMP-2诱导的骨形成。由载有BMP-2的聚乳酸-乙醇酸共聚物微球组成的复合物被包埋在被载有VEGF的明胶水凝胶包围的聚丙烯支架中,用于顺序释放生长因子。将空的复合材料或负载VEGF和/或BMP-2的复合材料异位和原位植入Sprague-Dawley大鼠(n = 9)。植入后,通过使用闪烁探针测量(125)I标记的生长因子的活性来确定局部释放曲线。 8周后,使用微血管造影,microCT和组织学分析血管和骨形成。支架在最初的3天之内表现出较大的VEGF初始爆发释放,并在整个56天的植入期内持续释放BMP-2。尽管VEGF不诱导骨形成,但确实增加了异位植入物中支持性血管网络的形成(p = 0.03)。与单独的BMP-2持续释放相结合,与单独的BMP-2相比,VEGF显着增强了异位骨形成(p = 0.008)。与单独的BMP-2相比,在原位缺损中,未发现VEGF对血管形成的影响,并且通过生长因子的组合也没有更高的骨形成。这项研究表明,顺序的血管生成和成骨生长因子释放可能有益于增强骨再生。

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