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苔藓纤维突触体在Percoll梯度上的亚细胞分级分离:对照和去颗粒大鼠海马体的形态学和生化特征

Subcellular fractionation on Percoll gradient of mossy fiber synaptosomes: morphological and biochemical characterization in control and degranulated rat hippocampus.

作者信息

Taupin P, Zini S, Cesselin F, Ben-Ari Y, Roisin M P

机构信息

INSERM U 29, Paris, France.

出版信息

J Neurochem. 1994 Apr;62(4):1586-95. doi: 10.1046/j.1471-4159.1994.62041586.x.

Abstract

A method for preparation of hippocampal mossy fiber synaptosomes directly from the postnuclear pellet is presented. This method represents an adaptation of that previously described for the isolation of synaptosomes by centrifugation through Percoll gradients directly from the supernatant fraction. We have characterized by electron microscopy two fractions, PII and PIII, enriched in mossy fiber synaptosomes; fraction PIII had 75% mossy fiber synaptosomes with well-preserved morphology (large size 3 microns, complex morphology, high synaptic vesicle density, multisynapses), whereas fraction PII contained 12%. These fractions were enriched in lactate dehydrogenase activity indicating that the integrity of synaptosomes was preserved. Compared with the other synaptosomal fractions, these fractions showed greater levels of dynorphin A (1-8) immunoreactivity and endogenous zinc, which are particularly concentrated in hippocampal mossy fiber terminals. Furthermore, we prepared synaptosomes from adult hippocampus after neonatal irradiation, which destroys the majority of granule cells and associated mossy fibers. The levels of dynorphin and zinc decreased by 88 and 70% in fraction PII and by 95 and 90%, respectively, in PIII. These results suggest that the rapid Percoll procedure is convenient for the purification of mossy fiber synaptosomes.

摘要

本文介绍了一种直接从核后沉淀中制备海马苔藓纤维突触体的方法。该方法是对先前描述的通过直接从上清液部分经Percoll梯度离心分离突触体方法的改进。我们通过电子显微镜对富含苔藓纤维突触体的两个组分PII和PIII进行了表征;组分PIII含有75%形态保存良好的苔藓纤维突触体(大尺寸3微米,形态复杂,突触小泡密度高,多突触),而组分PII含有12%。这些组分中乳酸脱氢酶活性增强,表明突触体的完整性得以保留。与其他突触体组分相比,这些组分显示出更高水平的强啡肽A(1-8)免疫反应性和内源性锌,它们特别集中在海马苔藓纤维终末。此外,我们从新生期受照射后的成年海马制备了突触体,这种照射破坏了大多数颗粒细胞和相关的苔藓纤维。组分PII中强啡肽和锌的水平分别下降了88%和70%,组分PIII中分别下降了95%和90%。这些结果表明,快速Percoll程序便于纯化苔藓纤维突触体。

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