Chamlian A, Benkoel L, Gulian J M, Bongrand P, Brisse J, Dalmasso C, Benoliel A M
Laboratoire d'Anatomie Pathologique et de Cytochimie, Faculté de Médecine, Marseille, France.
Cell Mol Biol. 1992 May;38(3):273-80.
Histochemical and cytochemical methods induce a loss of endoplasmic reticulum (ER) membrane integrity in hepatocytes. In order to evaluate the degree of ER membrane integrity, glucose-6-phosphatase (G6P-A) was localized in light and electron microscopy using glucose-6-phosphate (G6P) and mannose-6-phosphate (M6P) as substrates. In case of ER membrane alteration, M6P diffuses inside the ER and is hydrolysed by a non-specific phosphohydrolase. G6P and M6P hydrolysis was quantified with image analysis methods. In light microscopy, the ratio of reaction of M6P hydrolysis/G6P hydrolysis gave 75% of non specific reaction. In electron microscopic study this ratio was about 30%. These results showed that enzyme localization methods in electron microscopy produced less ER membrane alteration than light microscopic methods.
组织化学和细胞化学方法会导致肝细胞内质网(ER)膜完整性丧失。为了评估内质网膜完整性的程度,以葡萄糖-6-磷酸(G6P)和甘露糖-6-磷酸(M6P)为底物,通过光学显微镜和电子显微镜对葡萄糖-6-磷酸酶(G6P-A)进行定位。在内质网膜发生改变的情况下,M6P扩散到内质网内部,并被一种非特异性磷酸水解酶水解。采用图像分析方法对G6P和M6P的水解进行定量分析。在光学显微镜下,M6P水解反应/G6P水解反应的比值显示非特异性反应占75%。在电子显微镜研究中,该比值约为30%。这些结果表明,与光学显微镜方法相比,电子显微镜中的酶定位方法对内质网膜的改变较小。