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The enhanced angiogenesis effect of VEGF-silk fibroin nanospheres-BAMG scaffold composited with adipose derived stem cells in a rabbit model

机译:VEGF-丝素蛋白纳米球-BAMG支架与脂肪干细胞复合在兔模型中的血管新生作用增强

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摘要

We report a study to determine whether a vascular endothelial growth factor (VEGF)-silk fibroin (SF) nanospheres-bladder acellular matrix graft (BAMG) scaffold composited with adipose derived stem cells (ADSCs) could enhance angiogenesis in bladder regeneration in rabbits. Rabbit ADSCs were isolated and identified by flow cytometry. The morphology and release behaviour of VEGF-SF nanospheres were detected. After the composite scaffolds were successfully used in bladder reconstruction, the bladder capacity, H&E staining and immunohistochemical staining were studied at different time points. ADSCs exerts high expression rates of CD29, CD90, and CD44, accompanied with low expression rates of CD34 and CD45. SF nanospheres with diameters of 200–1000 nm were prepared to load VEGF, and they contributed to maintain the release of VEGF. The reconstructed bladder with VEGF-SF nanospheres-BAMG plus ADSCs had more regular smooth muscle tissue and blood vessels. Moreover, instead of differentiating into epithelial or vascular endothelial cells, ADSCs may be more likely to provide additional cytokines to enhance angiogenesis in the bladder regeneration process. The tissue engineered bladder constructed by BAMG modified by VEGF-SF nanospheres possessed high bio-compatibility and an enhanced angiogenesis effect, and could be used as an ideal biological material to repair bladder defects after being composited with ADSCs.
机译:我们报告了一项研究,以确定是否将血管内皮生长因子(VEGF)-丝素蛋白(SF)纳米球-膀胱脱细胞基质移植物(BAMG)支架与脂肪衍生干细胞(ADSCs)复合在一起可以增强兔膀胱再生中的血管生成。分离兔ADSC并通过流式细胞术鉴定。检测了VEGF-SF纳米球的形态和释放行为。在成功地将复合支架用于膀胱重建后,研究了在不同时间点的膀胱容量,H&E染色和免疫组织化学染色。 ADSC发挥CD29,CD90和CD44的高表达率,并伴随CD34和CD45的低表达率。制备直径为200–1000 nm的SF纳米球以加载VEGF,它们有助于维持VEGF的释放。 VEGF-SF纳米球-BAMG加ADSCs重建的膀胱具有更规则的平滑肌组织和血管。此外,ADSC可能分化为上皮或血管内皮细胞,而不是分化为上皮或血管内皮细胞,而是更有可能提供其他细胞因子来增强膀胱再生过程中的血管生成。 VEGF-SF纳米球修饰的BAMG构建的组织工程膀胱具有较高的生物相容性和增强的血管生成作用,可作为与ADSCs复合后修复膀胱缺损的理想生物材料。

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