Soong H, Fischbarg J, Iwamoto T
Invest Ophthalmol Vis Sci. 1978 Nov;17(11):1113-7.
A method for denuding Descemet's membrane by dissection of all overlying stroma, while preserving the corneal endothelial layer, was developed and evaluated. The technique consists in treating the stroma with trypsin and surgically removing the softened stromal layers. With an automated thickness-measuring technique, the endothelium-Descemet preparation was found to range from 23 to 42 micron in thickness. Endothelial cell morphology was normal under specular and light-transmission microscopic examinations. Under electron microscopy, the endothelial cells appeared intact, except for an increase in the number of intracellular vacuoles. Occasionally, small portions of an intercellular space were found to be mildly dilated, but the over-all integrity of the junctional complex was intact. In vitro, the viability of the preparation was comparable with that of a cornea with all layers intact. Endothelial resting membrane potentials, measured with intracellular microelectrodes, were found to be within the normal (33 +/- 2 mV) range. It is thus possible to obtain a viable endothelial layer, completely stripped of stroma.
我们研发并评估了一种在保留角膜内皮细胞层的同时,通过切除所有覆盖其上的基质来剥除后弹力层的方法。该技术包括用胰蛋白酶处理基质并手术切除软化的基质层。采用自动厚度测量技术,发现内皮 - 后弹力层制剂的厚度在23至42微米之间。在镜面反射和透光显微镜检查下,内皮细胞形态正常。在电子显微镜下,除了细胞内空泡数量增加外,内皮细胞看起来完整无损。偶尔发现细胞间空间的小部分有轻度扩张,但连接复合体的整体完整性完好。在体外,该制剂的活力与各层完整的角膜相当。用细胞内微电极测量的内皮静息膜电位在正常范围(33±2 mV)内。因此,有可能获得一个完全去除了基质的有活力的内皮细胞层。