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葡萄糖-6-磷酸脱氢酶在大鼠脊髓少突胶质细胞中富集。酶组织化学和免疫细胞化学研究。

Glucose-6-phosphate dehydrogenase is enriched in oligodendrocytes of the rat spinal cord. Enzyme histochemical and immunocytochemical studies.

作者信息

Kugler P

机构信息

Institute of Anatomy, University of Würzburg, Germany.

出版信息

Histochemistry. 1994 Feb;101(2):143-53. doi: 10.1007/BF00269361.

Abstract

Glucose-6-phosphate dehydrogenase (G6PD) was localized in rat spinal cord by catalytic enzyme histochemistry and immunocytochemistry. G6PD detected by either method was shown to be strongly enriched in cell bodies and processes of oligodendrocytes, whereas in the compact myelin G6PD was not detected. The enzyme histochemical procedure for the demonstration of G6PD was also adapted for microphotometric measurements of G6PD activity in the spinal cord white matter. There was a linear relationship between G6PD activity and section thickness up to 14 microns and between G6PD activity and reaction time up to 5-6 min as demonstrated by kinetic and end-point measurements. Significantly lower activities were measured in end-point measurements than in kinetic measurements because of formazan loss during rinsing. Methoxyphenazine methosulphate as an exogenous electron carrier and sodium azide as a blocker of the respiratory chain significantly increased the demonstrable G6PD activity. The Km was 0.62 mM and the Vmax 3 mumol glucose-6-phosphate/cm3 wet tissue and per min at 25 degrees C. It is concluded that G6PD in oligodendrocytes may be important for the generation of NADPH required for lipid biosynthesis related to myelogenesis, and reduction of glutathione required for protection of membrane sulphydryl groups.

摘要

通过催化酶组织化学和免疫细胞化学方法,将葡萄糖 -6-磷酸脱氢酶(G6PD)定位在大鼠脊髓中。结果显示,两种方法检测到的G6PD在少突胶质细胞的细胞体和突起中高度富集,而在致密髓鞘中未检测到G6PD。用于显示G6PD的酶组织化学方法也适用于对脊髓白质中G6PD活性进行显微光度测量。动力学和终点测量结果表明,G6PD活性与切片厚度在14微米以内呈线性关系,与反应时间在5 - 6分钟以内呈线性关系。由于漂洗过程中azan损失,终点测量中测得的活性明显低于动力学测量。作为外源电子载体的甲氧基吩嗪甲磺酸盐和作为呼吸链阻断剂的叠氮化钠显著增加了可检测到的G6PD活性。在25℃时,Km为0.62 mM,Vmax为3 μmol葡萄糖 -6-磷酸/立方厘米湿组织每分钟。结论是,少突胶质细胞中的G6PD对于与髓鞘形成相关的脂质生物合成所需的NADPH生成以及保护膜巯基所需的谷胱甘肽还原可能很重要。

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