Kahn C R, Young E, Lee I H, Rhim J S
Gillette Medical Evaluation Laboratories, Gaithersburg, MD 20879.
Invest Ophthalmol Vis Sci. 1993 Nov;34(12):3429-41.
To develop an in vitro model of human corneal epithelium that can be propagated in serum-free medium that is tissue specific, species specific, and continuously available.
Primary explant cultures from human cadaver donor corneas were generated and subsequently infected with Adeno 12-SV40 (Ad12-SV40) hybrid virus or transfected with plasmid RSV-T.
Several lines of human corneal epithelial cells with extended life span were developed and characterized. Propagation of both primary cultures and lines with extended life span, upon collagen membranes at an air-liquid interface, promoted multilayering, more closely approximating the morphology observed in situ.
In vitro models, using primary cultures of corneal epithelium and lines of corneal epithelial cells with extended life span, retain a variety of phenotypic characteristics and may be used as an adjunct to ocular toxicology studies and as a tool to investigate corneal epithelial cell biology.
建立一种人角膜上皮细胞的体外模型,该模型能够在无血清、组织特异性、物种特异性且可连续获取的培养基中增殖。
从人尸体供体角膜制备原代外植体培养物,随后用腺病毒12 - SV40(Ad12 - SV40)杂交病毒感染或用质粒RSV - T转染。
建立并鉴定了几株寿命延长的人角膜上皮细胞系。原代培养物和寿命延长的细胞系在气液界面的胶原膜上增殖,促进了多层化,更接近原位观察到的形态。
使用角膜上皮原代培养物和寿命延长的角膜上皮细胞系的体外模型保留了多种表型特征,可作为眼毒理学研究的辅助手段和研究角膜上皮细胞生物学的工具。