Cejková J, Lojda Z, Havránková E
Histochemistry. 1975 Sep 29;44(4):337-43. doi: 10.1007/BF00490370.
Activities of acid phosphatase, beta-glucuronidase, N-acethyl-beta-D-glucosaminidase and acid beta-galactosidase were investigated histochemically in rabbit corneas. Frozen sections after block fixation in cold 4% formaldehyde with 1% CaCl2 followed by washing in cold physiological saline as well as cold microtome sections of corneas quenched in petroleter chilled with acetone-dry ice mixture, transferred to nonprecooled slides or semipermeable membranes were used. Standard aqueous media were employed in the case of free-floating frozen sections of fixed corneas as well as of cold mictrotome sections (postfixed in cold 4% formaldehyde). Agar media were used in connection with the technic of semipermeable membranes. Gomori method (in the case of acid phosphatase), simultaneous azocoupling methods (substrates derivated of naphthol-AS-BI with hexazonium-p-rosanilin) in the case of acid phosphatase, beta-glucuronidase and N-acetyl-beta-D-glucosaminidase and the indigogenic method in the case of acid beta-galactosidase were applied. Enzyme activities in sections of fixed corneas were minimal in comparison with those in cold microtome sections of unfixed material revealed particularly with the technic of semipermeable membranes which is to be preferred. This technic is recommended in studies concerned with lysosomal enzymes in the cornea, particularly in keratocytes. All enzymes investigated were present in corneal epithelium, keratocytes and endothelium. Acid phosphatase displayed the highest activity followed by beta-glucuronidase and acetyl-beta-D-glucosaminidase. The activity of beta-galactosidase was the lowest. For the demonstration of activities in keratocytes sections parallel to the surface are very suitable. In these sections enzyme activities were demonstrated in small granules (apparently lysosomes) present in the central part of their cytoplasm as well as in projections. Diffuse staining was also seen, being the highest in the case of acid phosphatase.
采用组织化学方法研究了兔角膜中酸性磷酸酶、β-葡萄糖醛酸酶、N-乙酰-β-D-氨基葡萄糖苷酶和酸性β-半乳糖苷酶的活性。使用在含有1%氯化钙的冷4%甲醛中进行块固定后,经冷生理盐水冲洗的冰冻切片,以及在丙酮-干冰冷冻的石油醚中骤冷的角膜冷切片,将其转移至未预冷的载玻片或半透膜上。对于固定角膜的游离漂浮冰冻切片以及冷切片(在冷4%甲醛中后固定),使用标准水性介质。琼脂介质与半透膜技术结合使用。应用了Gomori法(用于酸性磷酸酶)、同时偶氮偶联法(萘酚-AS-BI衍生底物与对玫瑰红六偶氮盐)用于酸性磷酸酶、β-葡萄糖醛酸酶和N-乙酰-β-D-氨基葡萄糖苷酶,以及用于酸性β-半乳糖苷酶的靛蓝生成法。与未固定材料的冷切片相比,固定角膜切片中的酶活性最低,特别是在半透膜技术中尤为明显,该技术更受青睐。在研究角膜中的溶酶体酶,特别是角膜细胞中的溶酶体酶时,推荐使用该技术。所有研究的酶均存在于角膜上皮、角膜细胞和内皮中。酸性磷酸酶活性最高,其次是β-葡萄糖醛酸酶和乙酰-β-D-氨基葡萄糖苷酶。β-半乳糖苷酶的活性最低。对于显示角膜细胞中的活性,与表面平行的切片非常合适。在这些切片中,酶活性在其细胞质中央部分以及突起中存在的小颗粒(显然是溶酶体)中得到显示。还可见弥漫性染色,酸性磷酸酶的染色最高。