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

被引:57
|
作者
Zhang, Qixu [1 ]
Hubenak, Justin [1 ]
Iyyanki, Tejaswi [1 ]
Aired, Erik [1 ]
Turza, Kristin C. [1 ]
Davis, Greg [1 ]
Chang, Edward I. [1 ]
Branch-Brooks, Cynthia D. [1 ]
Beahm, Elisabeth K. [1 ]
Butler, Charles E. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Plast Surg, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
Soft tissue flap engineering; Adipose-derived stem cell; Vascular endothelial growth factor; PLGA/PEG microsphere; Collagen-chitosan scaffold; Vascularization; IN-VITRO CHARACTERIZATION; GROWTH-FACTOR-I; LONG-TERM; HYDROGEL CONSTRUCTS; LOCAL-DELIVERY; PROLIFERATION; CARRIERS; CHAMBER; INSULIN; MATRIX;
D O I
10.1016/j.biomaterials.2015.09.024
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
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.
引用
收藏
页码:198 / 213
页数:16
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