Low-temperature electrospun silk scaffold for in vitro mucosal modeling

被引:25
作者
Bulysheva, Anna A. [1 ,2 ]
Bowlin, Gary L. [2 ]
Klingelhutz, Aloysius J. [3 ,4 ]
Yeudall, W. Andrew [1 ,5 ]
机构
[1] Virginia Commonwealth Univ, VCU Philips Inst, Richmond, VA 23298 USA
[2] Virginia Commonwealth Univ, Dept Biomed Engn, Richmond, VA 23298 USA
[3] Univ Iowa, Dept Microbiol, Iowa City, IA 52242 USA
[4] Univ Iowa, Holden Comprehens Canc Ctr, Iowa City, IA 52242 USA
[5] Virginia Commonwealth Univ, Massey Canc Ctr, Richmond, VA 23298 USA
关键词
low-temperature electrospinning; cryogenic electrospinning; silk; cell infiltration; fibroblasts; keratinocytes; VIVO CELL INFILTRATION; POLY(D; L-LACTIDE); SCAFFOLD; NANOFIBERS; KERATINOCYTES; FABRICATION; EXPRESSION; PROTEINS;
D O I
10.1002/jbm.a.33288
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Electrospinning is often used to create scaffolding as a biomimetic of the extracellular matrix of tissues. A frequent limitation of this technique for three-dimensional tissue modeling is poor cell infiltration throughout the void volume of scaffolds. Here, we generated low-temperature electrospun silk scaffolds and compared these with conventional electrospun silk scaffolds in terms of mechanical properties, void volume, cell infiltration, cell viability, and potential to support mucosal models under three-dimensional culture conditions. Low-temperature electrospun silk scaffolds supported fibroblast attachment and infiltration throughout the volume of the scaffolds, while conventional electrospun scaffolds exhibited limited cell infiltration with fibroblasts attaching exclusively to the seeding surface of the scaffolds. The porosity of low-temperature electrospun scaffolds was 93% compared with 88% of conventional electrospun silk scaffolds. Uniaxial tensile testing showed a 3.5-fold reduction in strength of low-temperature electrospun silk compared with the conventional in terms of peak stress and modulus but no significant change in strain at break. Mucosal modeling with fibroblast-keratinocyte or fibroblast-carcinoma cocultures showed similar results, with cell infiltration occurring only in low-temperature electrospun scaffolds. Cell viability was confirmed using live/dead staining after 21 days in culture. Furthermore, low-temperature electrospun silk scaffolds were able to support keratinocyte differentiation, as judged by involucrin immunoreactivity. The low-temperature electrospun silk scaffold that we have developed eliminates the limitation of electrospun silk scaffolds in terms of cell infiltration and, therefore, can potentially be used for a wide range of tissue engineering purposes ranging from in vitro tissue modeling to in vivo tissue regeneration purposes. (C) 2012 Wiley Periodicals, Inc. J Biomed Mater Res Part A, 2012.
引用
收藏
页码:757 / 767
页数:11
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