Higa Kazunari, Takeshima Naomi, Moro Fumika, Kawakita Tetsuya, Kawashima Motoko, Demura Makoto, Shimazaki Jun, Asakura Tetsuo, Tsubota Kazuo, Shimmura Shigeto
a Department of Ophthalmology and Cornea Center, Tokyo Dental College, Sugano 5-11-13, Chiba 272-8513, Japan; Department of Ophthalmology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku, Tokyo 160-8582, Japan.
J Biomater Sci Polym Ed. 2011;22(17):2261-76. doi: 10.1163/092050610X538218.
Biological carriers, such as the amniotic membrane and serum-derived fibrin, are currently used to deliver cultivated corneal epithelial sheets to the ocular surface. Such carriers require being transparent and allowing the diffusion of metabolites in order to maintain a healthy ocular surface. However, safety issues concerning biological agents encouraged the development of safer, biocompatible materials as cell carriers. We examined the application of porous silk fibroin films with high molecular permeability prepared by mixing silk fibroin and poly(ethylene glycol) (PEG), and then removal of PEG from the silk-PEG films. Molecular permeability of porous silk fibroin film is higher than untreated silk fibroin film. Epithelial cells were isolated from rabbit limbal epithelium, and seeded onto silk fibroin coated wells and co-cultured with mitomycin C-treated 3T3 fibroblasts. Stratified epithelial sheets successfully engineered on porous silk fibroin film expressed the cornea-specific cytokeratins K3 and K12, as well as the corneal epithelial marker pax6. Basement membrane components such as type-IV collagen and integrin β1 were expressed in the stratified epithelial sheets. Further more, colony-forming efficiency of dissociated cells was similar to primary corneal epithelial cells showing that progenitor cells were preserved. The biocompatibility of fibroin films was confirmed in rabbit corneas for up to 6 months. Porous silk fibroin film is a highly transparent, biocompatible material that may be useful as a carrier of cultivated epithelial sheets in the regeneration of corneal epithelium.
生物载体,如羊膜和血清来源的纤维蛋白,目前被用于将培养的角膜上皮片递送至眼表。这类载体需要具备透明性并允许代谢产物扩散,以维持健康的眼表。然而,与生物制剂相关的安全问题促使人们研发更安全、具有生物相容性的材料作为细胞载体。我们研究了通过将丝素蛋白与聚乙二醇(PEG)混合,然后从丝素-PEG膜中去除PEG制备的具有高分子渗透性的多孔丝素蛋白膜的应用。多孔丝素蛋白膜的分子渗透性高于未处理的丝素蛋白膜。从兔角膜缘上皮分离出上皮细胞,接种到涂有丝素蛋白的孔中,并与丝裂霉素C处理的3T3成纤维细胞共培养。在多孔丝素蛋白膜上成功构建的分层上皮片表达角膜特异性细胞角蛋白K3和K12以及角膜上皮标志物pax6。分层上皮片中表达了IV型胶原和整合素β1等基底膜成分。此外,解离细胞的集落形成效率与原代角膜上皮细胞相似,表明祖细胞得以保留。丝素蛋白膜在兔角膜中的生物相容性在长达6个月的时间内得到了证实。多孔丝素蛋白膜是一种高度透明、具有生物相容性的材料,可能作为培养上皮片的载体用于角膜上皮再生。