Daniels K K, Vickroy T W
Department of Neuroscience, University of Florida, Gainesville 32610, USA.
Neurochem Res. 1998 Jan;23(1):103-13. doi: 10.1023/a:1022413823183.
An improved three-step Percoll density gradient centrifugation technique is described for simultaneous isolation of glial plasmalemmal vesicles (GPV) and synaptosomal vesicles (SYN) from a rat brain homogenate. While electron microscopy revealed that fractions contained intact vesicles with markedly distinct morphological features, measures of high-affinity [3H]choline uptake, glutamine synthetase and carbonic anhydrase activities, as well as Western blot analyses for glial fibrillary acidic protein and neuron specific enolase, served to confirm the low level of neuronal contamination in GPV fractions as well as the low level of glial contamination in SYN fractions. In addition, GPV and SYN fractions were used to characterize the kinetic and pharmacological properties of sodium-dependent [3H]L-glutamate transport. In conclusion, these results demonstrate the usefulness of this method for obtaining highly-enriched, functionally viable populations of glial and neuronal elements which are suitable for studies of their respective cell functions in vitro.
本文描述了一种改进的三步Percoll密度梯度离心技术,用于从大鼠脑匀浆中同时分离神经胶质细胞质膜囊泡(GPV)和突触体囊泡(SYN)。电子显微镜显示,各组分含有形态明显不同的完整囊泡,而通过高亲和力[3H]胆碱摄取、谷氨酰胺合成酶和碳酸酐酶活性的测定,以及对胶质纤维酸性蛋白和神经元特异性烯醇化酶的蛋白质免疫印迹分析,证实了GPV组分中神经元污染水平较低,以及SYN组分中神经胶质污染水平较低。此外,GPV和SYN组分用于表征钠依赖性[3H]L-谷氨酸转运的动力学和药理学特性。总之,这些结果证明了该方法对于获得高度富集、功能上可行的神经胶质和神经元成分群体的有用性,这些群体适用于体外研究它们各自的细胞功能。