Min Byung-Moo, Jeong Lim, Nam Young Sik, Kim Jin-Man, Kim Jin Young, Park Won Ho
Department of Oral Biochemistry and Dental Research Institute, IBEC and BK21 HLS, College of Dentistry, Seoul National University, Seoul 110-749, Republic of Korea.
Int J Biol Macromol. 2004 Oct;34(5):281-8. doi: 10.1016/j.ijbiomac.2004.08.004.
Three forms of silk fibroin (SF) matrices, woven (microfiber), non-woven (nanofiber), and film form, were used to perform a conformational analysis and cell culture using normal human oral keratinocytes (NHOK). To obtain the SF microfiber (SF-M) matrix, natural grey silk was degummed, while the SF film (SF-F) and nanofiber (SF-N) matrices were prepared by casting and electrospinning the formic acid solutions of the regenerated SF, respectively. For insolubilization, as-prepared SF-F and SF-N matrices were chemically treated with an aqueous methanol solution of 50%. The conformational structures of as-prepared and chemically treated SF matrices were investigated using attenuated total reflectance infrared spectroscopy (ATR-IR) and solid-state 13C CP/MAS nuclear magnetic resonance (NMR) spectroscopy. The as-cast SF-F matrix formed a mainly beta-sheet structure that was similar to the SF-M matrix, whereas the as-spun SF-N matrix had a random coil conformation as the predominant secondary structure. Conformational transitions from random coil to beta-sheet of the as-spun SF-N occurred rapidly within 10 min following aqueous methanol treatment, and were confirmed by solid-state 13C NMR analysis. To assess the cytocompatibility and cells behavior on the different textures of SF, we examined the cell attachment and spreading of NHOK that was seeded onto the SF matrices, as well as the interaction between the cells and SF matrices. Our results indicate that the SF nanofiber matrix may be more preferable than SF film and SF microfiber matrices for biomedical applications, such as wound dressings and scaffolds for tissue engineering.
使用三种形式的丝素蛋白(SF)基质,即编织(微纤维)、非编织(纳米纤维)和薄膜形式,对正常人口腔角质形成细胞(NHOK)进行构象分析和细胞培养。为了获得SF微纤维(SF-M)基质,对天然生丝进行脱胶,而SF薄膜(SF-F)和纳米纤维(SF-N)基质分别通过浇铸和静电纺丝再生SF的甲酸溶液制备。为了使其不溶解,对制备好的SF-F和SF-N基质用50%的甲醇水溶液进行化学处理。使用衰减全反射红外光谱(ATR-IR)和固态13C CP/MAS核磁共振(NMR)光谱研究制备好的和化学处理后的SF基质的构象结构。浇铸得到的SF-F基质形成了主要为β-折叠结构,与SF-M基质相似,而静电纺丝得到的SF-N基质以无规卷曲构象作为主要二级结构。纺丝态的SF-N在甲醇水溶液处理后的10分钟内迅速发生从无规卷曲到β-折叠的构象转变,并通过固态13C NMR分析得到证实。为了评估SF不同质地对细胞相容性和细胞行为的影响,我们检测了接种在SF基质上的NHOK的细胞附着和铺展情况,以及细胞与SF基质之间的相互作用。我们的数据表明,对于生物医学应用,如伤口敷料和组织工程支架来说,SF纳米纤维基质可能比SF薄膜和SF微纤维基质更合适。