Three Dimensional Collagen Scaffold Promotes Intrinsic Vascularisation for Tissue Engineering Applications

被引:115
作者
Chan, Elsa C. [1 ,2 ]
Kuo, Shyh-Ming [3 ]
Kong, Anne M. [4 ]
Morrison, Wayne A. [4 ,5 ,6 ]
Dusting, Gregory J. [1 ,2 ,4 ]
Mitchell, Geraldine M. [4 ,5 ,6 ]
Lim, Shiang Y. [4 ,5 ]
Liu, Guei-Sheung [1 ,2 ]
机构
[1] Royal Victorian Eye & Ear Hosp, Ctr Eye Res Australia, East Melbourne, Vic, Australia
[2] Univ Melbourne, Dept Surg, Ophthalmol, East Melbourne, Vic, Australia
[3] I Shou Univ, Dept Biomed Engn, Kaohsiung, Taiwan
[4] St Vincents Inst Med Res, OBrien Inst Dept, 41 Victoria Parade, Fitzroy, Vic 3065, Australia
[5] Univ Melbourne, St Vincents Hosp Melbourne, Dept Surg, Fitzroy, Vic 3065, Australia
[6] Australian Catholic Univ, Fac Hlth Sci, Fitzroy, Vic, Australia
基金
英国医学研究理事会;
关键词
STEM-CELLS; IN-VITRO; ENHANCES SURVIVAL; ENDOTHELIAL-CELLS; CARDIAC TISSUE; ANGIOGENESIS; VIVO; MATRIX; DIFFERENTIATION; POPULATION;
D O I
10.1371/journal.pone.0149799
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Here, we describe a porous 3-dimensional collagen scaffold material that supports capillary formation in vitro, and promotes vascularization when implanted in vivo. Collagen scaffolds were synthesized from type I bovine collagen and have a uniform pore size of 80 mu m. In vitro, scaffolds seeded with primary human microvascular endothelial cells suspended in human fibrin gel formed CD31 positive capillary-like structures with clear lumens. In vivo, after subcutaneous implantation in mice, cell-free collagen scaffolds were vascularized by host neovessels, whilst a gradual degradation of the scaffold material occurred over 8 weeks. Collagen scaffolds, impregnated with human fibrinogen gel, were implanted subcutaneously inside a chamber enclosing the femoral vessels in rats. Angiogenic sprouts from the femoral vessels invaded throughout the scaffolds and these degraded completely after 4 weeks. Vascular volume of the resulting constructs was greater than the vascular volume of constructs from chambers implanted with fibrinogen gel alone (42.7 +/- 5.0 mu L in collagen scaffold vs 22.5 +/- 2.3 mu L in fibrinogen gel alone; p < 0.05, n = 7). In the same model, collagen scaffolds seeded with human adipose-derived stem cells (ASCs) produced greater increases in vascular volume than did cell-free collagen scaffolds (42.9 +/- 4.0 mu L in collagen scaffold with human ASCs vs 25.7 +/- 1.9 mu L in collagen scaffold alone; p < 0.05, n = 4). In summary, these collagen scaffolds are biocompatible and could be used to grow more robust vascularized tissue engineering grafts with improved the survival of implanted cells. Such scaffolds could also be used as an assay model for studies on angiogenesis, 3-dimensional cell culture, and delivery of growth factors and cells in vivo.
引用
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页数:15
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