Assimilating cell sheets and hybrid scaffolds for dermal tissue engineering

被引:21
|
作者
Ng, KW
Tham, W
Lim, TC
Hutmacher, DW
机构
[1] Natl Univ Singapore, Div Bioengn, Singapore 117576, Singapore
[2] Natl Univ Singapore, Dept Orthopaed Surg, Singapore 119074, Singapore
[3] Natl Univ Singapore, Dept Surg, Singapore 117576, Singapore
[4] Natl Univ Singapore, Dept Biol Sci, Singapore 117576, Singapore
[5] Natl Univ Singapore Hosp, Dept Plast Surg, Singapore 117576, Singapore
关键词
skin; extracellular matrix; poly(lactic-co-glycolic acid); collagen; tissue engineering;
D O I
10.1002/jbm.a.30454
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Cell sheets can be used to produce neo-tissue with mature extracellular matrix. However, extensive contraction of cell sheets remains a problem. We devised a technique to overcome this problem and applied it to tissue engineer a dermal construct. Human dermal fibroblasts were cultured with poly(lactic-co-glycolic acid)-collagen meshes and collagen-hyaluronic acid foams. Resulting cell sheets were folded over the scaffolds to form dermal constructs. Human keratinocytes were cultured on these dermal constructs to assess their ability to support bilayered skin regeneration. Dermal constructs produced with collagen-hyaluronic acid foams showed minimal contraction, while those with poly(lactic-co-glycolic acid)-collagen meshes curled up. Cell proliferation and metabolic activity profiles were characterized with PicoGreen (R) and AlamarBlue (TM) assays, respectively. Fluorescent labeling showed high cell viability and F-actin expression within the constructs. Collagen deposition was detected by immunocytochemistry and electron microscopy. Transforming Growth Factor-alpha and beta 1, Keratinocyte Growth Factor and Vascular Endothelial Growth Factor were produced at various stages of culture, measured by RT-PCR and ELISA. These results indicated that assimilating cell sheets with mechanically stable scaffolds could produce viable dermal-like constructs that do not contract. Repeated enzymatic treatment cycles for cell expansion is unnecessary, while the issue of poor cell seeding efficiency in scaffolds is eliminated. (c) 2005 Wiley Periodicals, Inc.
引用
收藏
页码:425 / 438
页数:14
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