Growth of mesenchymal stem cells on electrospun type I collagen nanofibers

被引:242
作者
Shih, Yu-Ru V.
Chen, Chung-Nan
Tsai, Shiao-Wen
Wang, Yng Jiin
Lee, Oscar K.
机构
[1] Taipei Vet Gen Hosp, Dept Orthopaed & Traumatol, Taipei, Taiwan
[2] Natl Yang Ming Univ, Inst Biopharmaceut Sci, Taipei 112, Taiwan
[3] Ind Technol Res Inst, Biomed Engn Res Lab, Hsinchu, Taiwan
[4] Chang Gung Univ, Inst Biochem & Biomed Engn, Taoyuan, Taiwan
[5] Natl Yang Ming Univ, Inst Biomed Engn, Taipei 112, Taiwan
[6] Taipei Vet Gen Hosp, Dept Med Res & Educ, Taipei, Taiwan
[7] Natl Yang Ming Univ, Sch Med, Taipei 112, Taiwan
关键词
mesenchymal stem cells; electrospin; nanofibers; type I collagen; focal adhesion;
D O I
10.1634/stemcells.2006-0253
中图分类号
Q813 [细胞工程];
学科分类号
摘要
We reconstituted type I collagen nanofibers prepared by electrospin technology and examined the morphology, growth, adhesion, cell motility, and osteogenic differentiation of human bone marrow-derived mesenchymal stem cells (MSCs) on three nano-sized diameters (50-200, 200 500, and 500-1,000 nm). Results from scanning electron microscopy showed that cells on the nanofibers had a more polygonal and flattened cell morphology. MTS (3-[4,5-dimethythiazol-2-yl]-5-[3-carboxy-methoxyphenyl]-2-[4-sulfophenyl]2H-tetrazolium compound) assay demonstrated that the MSCs grown on 500-1,000-nm nanofibers had significantly higher cell viability than the tissue culture polystyrene control. A decreased amount of focal adhesion formation was apparent in which quantifiable staining area of the cytoplasmic protein vinculin for the 200-500-nm nanofibers was 39% less compared with control, whereas the area of quantifiable vinculin staining was 45% less for both the 200-500-nm and 500-1,000-nm nanofibers. The distances of cell migration were quantified on green fluorescent protein-nucleofected cells and was 56.7%, 37.3%, and 46.3% for 50-200, 200-500, and 500-1,000 nm, respectively, compared with those on the control. Alkaline phosphatase activity demonstrated no differences after 12 days of osteogenic differentiation, and reverse transcription-polymerase chain reaction (RT-PCR) analysis showed comparable osteogenic gene expression of osteocalcin, osteonectin, and ostepontin between cells differentiated on polystyrene and nanofiber surfaces. Moreover, single-cell RT-PCR of type I collagen gene expression demonstrated higher expression on cells seeded on the nanofibers. Therefore, type I collagen nanofibers support the growth of MSCs without compromising their osteogenic differentiation capability and can be used as a scaffold for bone tissue engineering to facilitate intramembranous bone formation. Further efforts are necessary to enhance their biomimetic properties.
引用
收藏
页码:2391 / 2397
页数:7
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