Minami Y, Sugihara H, Oono S
Department of Pathology, Saga Medical School, Japan.
Invest Ophthalmol Vis Sci. 1993 Jun;34(7):2316-24.
To report on an in vitro reconstruction of cornea composed of three main layers.
These layers were reconstructed from isolated bovine corneal cells in three-dimensional collagen gel culture conditions.
The topmost layer, corneal epithelial cells on collagen gel, was treated by what was designated as the "air-liquid interface method," a method developed specifically for this study. The treatment induced proliferation and differentiation of this layer. Those epithelial cells were positively immunostained with anti-epithelial keratin (55-kD/64-kD) antibody, AE5, which was specific for in vivo corneal epithelial cells. The middle layer consisted of keratocytes in the three-dimensional collagen gel matrix. This layer was comparable to the stroma in vivo. The underlayer, the counterpart of in vivo endothelial layer, was composed of corneal endothelial cells.
This culture system probably provides a physiologic environment for detailed investigations of corneal cells.
报告一种由三个主要层次组成的角膜体外重建方法。
这些层次是在三维胶原凝胶培养条件下,由分离的牛角膜细胞重建而成。
最上层,即胶原凝胶上的角膜上皮细胞,采用了专门为本研究开发的“气液界面法”进行处理。该处理诱导了这一层的增殖和分化。这些上皮细胞用抗上皮角蛋白(55-kD/64-kD)抗体AE5进行阳性免疫染色,AE5对体内角膜上皮细胞具有特异性。中间层由三维胶原凝胶基质中的角膜细胞组成。这一层与体内的基质相当。底层,即体内内皮细胞层的对应物,由角膜内皮细胞组成。
该培养系统可能为角膜细胞的详细研究提供一个生理环境。