首页> 外文期刊>Biomaterials >Engineering vascularized soft tissue flaps in an animal model using human adipose derived stem cells and VEGF plus PLGA/PEG microspheres on a collagen-chitosan scaffold with a flow-through vascular pedicle
【24h】

Engineering vascularized soft tissue flaps in an animal model using human adipose derived stem cells and VEGF plus PLGA/PEG microspheres on a collagen-chitosan scaffold with a flow-through vascular pedicle

机译:使用人脂肪衍生的干细胞和VEGF加上PLGA / PEG微球在具有流动性血管蒂的胶原壳聚糖支架上在动物模型中工程化血管化的软组织皮瓣

获取原文
获取原文并翻译 | 示例
           

摘要

Insufficient neovascularization is associated with high levels of resorption and necrosis in autologous and engineered fat grafts. We tested the hypothesis that incorporating angiogenic growth factor into a scaffold-stem cell construct and implanting this construct around a vascular pedicle improves neovascularization and adipogenesis for engineering soft tissue flaps. Poly(lactic-co-glycolic-acid/polyethylene glycol (PLGA/PEG) microspheres containing vascular endothelial growth factor (VEGF) were impregnated into collagen-chitosan scaffolds seeded with human adipose-derived stem cells (hASCs). This setup was analyzed in vitro and then implanted into isolated chambers around a discrete vascular pedicle in nude rats. Engineered tissue samples within the chambers were harvested and analyzed for differences in vascularization and adipose tissue growth. In vitro testing showed that the collagen-chitosan scaffold provided a supportive environment for hASC integration and proliferation. PLGA/PEG microspheres with slow-release VEGF had no negative effect on cell survival in collagen-chitosan scaffolds. In vivo, the system resulted in a statistically significant increase in neovascularization that in turn led to a significant increase in adipose tissue persistence after 8 weeks versus control constructs. These data indicate that our model-hASCs integrated with a collagen-chitosan scaffold incorporated with VEGF-containing PLGA/PEG microspheres supported by a predominant vascular vessel inside a chamber-provides a promising, clinically translatable platform for engineering vascularized soft tissue flap. The engineered adipose tissue with a vascular pedicle could conceivably be transferred as a vascularized soft tissue pedicle flap or free flap to a recipient site for the repair of soft-tissue defects. (C) 2015 Elsevier Ltd. All rights reserved.
机译:自体和工程脂肪移植物中新血管形成不足与高水平的吸收和坏死有关。我们测试了以下假设,即将血管生成生长因子整合到支架干细胞构建体中,并将​​该构建体植入血管蒂周围可以改善新血管形成和成脂,从而工程化软组织皮瓣。将含有血管内皮生长因子(VEGF)的聚乳酸-乙醇酸/聚乙二醇(PLGA / PEG)微球浸入植入人脂肪干细胞(hASCs)的胶原壳聚糖支架中。体外,然后将其植入裸鼠离散血管蒂周围的隔离腔中,收集腔室内的工程组织样本并分析其血管形成和脂肪组织生长的差异,体外测试表明胶原壳聚糖支架为小鼠提供了支持性环境。 hASC整合和增殖:缓慢释放VEGF的PLGA / PEG微球对胶原壳聚糖支架的细胞存活没有负面影响,在体内,该系统导致新血管形成的统计显着增加,进而导致脂肪显着增加与对照组相比,第8周后的组织持续存在。这些数据表明我们的hASCs模型与胶原-壳聚糖支架与腔室内主要血管支持的含VEGF的PLGA / PEG微球相结合,为工程化血管化的软组织皮瓣提供了有希望的,可临床翻译的平台。可以想到,具有血管蒂的工程化脂肪组织可以作为血管化的软组织蒂皮瓣或游离皮瓣转移到接受部位,以修复软组织缺损。 (C)2015 Elsevier Ltd.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号