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使用光镜和电镜联合程序在大鼠肝脏未固定的低温切片中显示5'-核苷酸酶活性。

Demonstration of 5'-nucleotidase activity in unfixed cryostat sections of rat liver using a combined light- and electron-microscope procedure.

作者信息

Song J, Bosch K S, Tigchelaar W, Van Den Munckhof R J, Schellens J P, Van Noorden C J, Frederiks W M

机构信息

Academic Medical Centre, University of Amsterdam, The Netherlands.

出版信息

Histochem J. 1995 Nov;27(11):914-22.

PMID:8787970
Abstract

In the present study a technique was developed to demonstrate 5'-nucleotidase activity in unfixed cryostat sections of rat liver at the light- and electron-microscope level using a semipermeable membrane. In order to retain the ultrastructure of the unfixed material as much as possible, incubations were also performed at 4 degrees C rather than at 37 degrees C. The optimized incubation medium contained 300 mM Tris-maleate buffer, pH 7.2, 5 mM adenosine monophosphate as substrate, 30 mM cerium chloride as capturing agent for liberated phosphate, 10 mM magnesium chloride as activator and 1.5% agar. At the light-microscope level, similar localizations of 5'-nucleotidase activity were obtained when incubations were performed at 37 degrees C and 4 degrees C. Enzyme activity was present mainly at bile canalicular membranes and at sinusoidal membranes of hepatocytes; total activity was higher in pericentral than in periportal areas. Cytophotometric analyses revealed that specific formation of final reaction product (FRP) (test minus control reaction) at 37 degrees C followed a hyperbolic curve with time. A linear relationship was found between specific amounts of FRP and section thickness up to 8 micrograms. 5'-Nucleotidase activity was about three-fold higher after incubation for 30 min at 37 degrees C than at 4 degrees C. At the electron-microscope level, it was demonstrated that the ultrastructure of rat liver was rather well-preserved after incubating unfixed cryostat sections attached to a semipermeable membrane and electron-dense FRP was found at bile canalicular and sinusoidal plasma membrane of hepatocytes. The most distinct changes in ultrastructure after incubation at 37 degrees C, in comparison with that at 4 degrees C, were the appearance of multi-lamellar structures at bile canaliculi at 37 degrees C. We conclude that the present method is valid for the demonstration of 5'-nucleotidase activity in unfixed cryostat sections of rat liver at both the light- and electron-microscope levels and that hypothermic incubations improve ultrastructural morphology substantially.

摘要

在本研究中,开发了一种技术,可在光镜和电镜水平上,使用半透膜在大鼠肝脏未固定的低温切片中显示5'-核苷酸酶活性。为了尽可能保留未固定材料的超微结构,孵育也在4℃而非37℃下进行。优化的孵育培养基含有300 mM马来酸三羟甲基氨基甲烷缓冲液,pH 7.2,5 mM腺苷一磷酸作为底物,30 mM氯化铈作为释放磷酸盐的捕获剂,10 mM氯化镁作为激活剂和1.5%琼脂。在光镜水平上,当在37℃和4℃下进行孵育时,获得了相似的5'-核苷酸酶活性定位。酶活性主要存在于胆小管膜和肝细胞的窦状膜;中央周围区域的总活性高于门周区域。细胞光度分析显示,在37℃下最终反应产物(FRP)的特异性形成(测试减去对照反应)随时间呈双曲线。在高达8微克的FRP特定量与切片厚度之间发现了线性关系。在37℃孵育30分钟后,5'-核苷酸酶活性比在4℃下高约三倍。在电镜水平上,证明了附着在半透膜上的未固定低温切片孵育后,大鼠肝脏的超微结构保存相当良好,并且在肝细胞的胆小管和窦状质膜处发现了电子致密的FRP。与在4℃下孵育相比,在37℃下孵育后超微结构最明显的变化是在37℃下胆小管出现多层结构。我们得出结论,本方法对于在光镜和电镜水平上显示大鼠肝脏未固定低温切片中的5'-核苷酸酶活性是有效的,并且低温孵育可显著改善超微结构形态。

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