Adipose tissue engineering in vivo with adipose-derived stem cells on naturally derived scaffolds

被引:45
|
作者
Flynn, L. [1 ]
Prestwich, G. D. [2 ,3 ]
Semple, J. L. [4 ,5 ,6 ]
Woodhouse, K. A. [1 ,6 ,7 ]
机构
[1] Univ Toronto, Dept Chem Engn & Appl Chem, Toronto, ON M5S 3E5, Canada
[2] Univ Utah, Ctr Therapeut Biomat, Salt Lake City, UT 84108 USA
[3] Univ Utah, Dept Med Chem, Salt Lake City, UT 84108 USA
[4] Univ Toronto, Div Plast Surg, Dept Surg, Toronto, ON M5G 1L5, Canada
[5] Womens Coll Hosp, Toronto, ON M5S 1B2, Canada
[6] Sunnybrook Hlth Sci Ctr, Adv Regenerat Tissue Engn Ctr, Toronto, ON M4N 3M5, Canada
[7] Queens Univ, Dept Chem Engn, Kingston, ON K7L 3N6, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
adipose tissue engineering; scaffold; extracellular matrix; hyaluronan; stem cells; GENE-EXPRESSION; HYALURONAN; DIFFERENTIATION; BREAST; RECONSTRUCTION; IMPLANTATION; MATRICES; MICE;
D O I
10.1002/jbm.a.32044
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Placental decellular matrix (PDM) and PDM combined with cross-linked hyaluronan (XLHA) scaffolds, seeded with primary human adipose-derived stem cells (ASC), were investigated in a subcutaneous athymic mouse model. The in vivo response at 3 and 8 weeks was characterized using histological and immunohistochemical staining. Fibrous capsule formation was assessed and the relative number of adipocytes in each scaffold was quantified. Undifferentiated ASC were localized using immunostaining for human vimentin. Unilocular and multilocular adipocytes were identified by intracellular lipid accumulation. Staining for murine CD31 assessed implant vascularization. Both scaffolds macroscopically maintained their three-dimensional volume and supported mature adipocyte populations in vivo. There was evidence of implant integration and a host contribution to the adipogenic response. The results Suggested that incorporating the XLHA had a positive effect in terms of angiogenesis and adipogenesis. Overall, the PDM and PDM with XLHA scaffolds showed great promise for adipose tissue regeneration. (c) 2008 Wiley Periodicals, Inc. J Biomed Mater Res 89A: 929-941, 2009
引用
收藏
页码:929 / 941
页数:13
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