Eniwumide Joshua O, Tanaka Masaru, Nagai Nobuhiro, Morita Yuka, de Bruijn Joost, Yamamoto Sadaaki, Onodera Shin, Kondo Eiji, Yasuda Kazunori, Shimomura Masatsugu
Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, 2-1-1. Katahira, Aoba-ku, Sendai 980-8577, Japan.
Creative Research Initiative "Sousei" (CRIS), Hokkaido University, N21 W10 Kita-ku, Sapporo 001-0021, Japan ; Department of Biochemical Engineering, Graduate School of Science and Engineering, Yamagata University, 4-3-16 Jonan, Yonezawa 992-8510, Japan.
Biomed Res Int. 2014;2014:710354. doi: 10.1155/2014/710354. Epub 2014 Apr 6.
The present study investigated the potential of a novel micropatterned substrate for neocartilage formation. Articular chondrocytes were cultured on poly( ɛ-caprolactone) materials whose surfaces were either flat or honeycomb-patterned. The latter was prepared using a novel self-organization technique, while the former, was prepared by spin-coating. The chondrocytes attached and proliferated on both surfaces. On the honeycomb films, chondrocytes were found at the top surface and encased within the 10 μm pores. Meanwhile, chondrocytes on the spin-coated surface flattened out. Accumulation of DNA and keratin sulphate was comparatively higher on the honeycomb films within the first 7 days. At their respective peaks, DNA concentration increased on the honeycomb and flat surfaces by approximately 210% and 400% of their day 1 values, respectively. However, cultures on the flat surface took longer to peak. Extracellular Matrix (ECM) concentrations peaked at 900% and 320% increases for the honeycomb and flat cultures. Type II collagen was upregulated on the honeycomb and flat surfaces by as much as 28% and 25% of their day 1 values, while aggrecan was downregulated with time, by 3.4% and 7.4%. These initial results demonstrate the potential usefulness of honeycomb-based scaffolds during early cultures neocartilage and soft tissue engineering.
本研究调查了一种新型微图案化基质用于新软骨形成的潜力。将关节软骨细胞培养在聚(ε-己内酯)材料上,其表面要么是平坦的,要么是蜂窝状图案的。后者使用一种新型自组装技术制备,而前者通过旋涂制备。软骨细胞在两种表面上均能附着并增殖。在蜂窝状薄膜上,软骨细胞出现在顶面并被包裹在10μm的孔隙内。同时,旋涂表面上的软骨细胞变扁平。在最初的7天内,蜂窝状薄膜上DNA和硫酸角质素的积累相对较高。在各自的峰值时,蜂窝状和平坦表面上的DNA浓度分别比第1天的值增加了约210%和400%。然而,平坦表面上的培养物达到峰值所需的时间更长。细胞外基质(ECM)浓度在蜂窝状和平坦培养物中分别达到900%和320%的峰值增长。II型胶原蛋白在蜂窝状和平坦表面上分别上调至第1天值的28%和25%,而聚集蛋白聚糖随时间下调,分别下调3.4%和7.4%。这些初步结果证明了基于蜂窝状的支架在新软骨早期培养和软组织工程中的潜在用途。