Azar D T, Spurr-Michaud S J, Tisdale A S, Gipson I K
Eye Research Institute of the Retina Foundation, Boston, MA 02114.
Arch Ophthalmol. 1989 Oct;107(10):1520-3. doi: 10.1001/archopht.1989.01070020594047.
Morphometric measurements of epithelial adhesion structures were performed on electron micrographs of corneas of diabetic patients (ages 35 to 77 years) and controls of similar age (ages 21 to 79 years). Penetration of the anchoring fibrils from the deepest layer of the basal lamina into the stroma was significantly decreased in diabetics (0.41 +/- 0.02 microns) compared with controls of similar ages (0.65 +/- 0.03 microns). Significant thickening of the basal lamina in diabetics (50.1 +/- 7.6 microns 2/100 microns basal cell membrane) was noted compared with controls (32.0 +/- 6.3 microns 2/100 microns), but no significant differences were noted in the percentage of the basal cell membrane occupied by hemidesmosomes. Decreased penetration of the anchoring fibrils into the stroma may cause the loose adhesion between the stroma and basement membrane observed in diabetes.
对糖尿病患者(年龄35至77岁)及年龄相仿的对照组(年龄21至79岁)角膜的电子显微照片进行上皮黏附结构的形态测量。与年龄相仿的对照组(0.65±0.03微米)相比,糖尿病患者中锚定原纤维从基底膜最深层向基质的穿透显著减少(0.41±0.02微米)。与对照组(32.0±6.3平方微米/100微米基底细胞膜)相比,糖尿病患者的基底膜显著增厚(50.1±7.6平方微米/100微米基底细胞膜),但在半桥粒占据的基底细胞膜百分比方面未观察到显著差异。锚定原纤维向基质的穿透减少可能导致糖尿病中观察到的基质与基底膜之间的黏附松散。