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大鼠脑神经元胞体和全神经胶质:一种新的分离技术。

Neuronal soma and whole neuroglia of rat brain: a new isolation technique.

作者信息

Norton W T, Poduslo S E

出版信息

Science. 1970 Feb 20;167(3921):1144-5. doi: 10.1126/science.167.3921.1144.

Abstract

Minced rat brain softened by treatment with trypsin is disrupted by filtration through nylon and steel meshes to produce a suspension of free-floating cells and debris. The cells are separated and purified by centrifugation on discontinuous sucrose gradients. Preparations of neuronal perikarya, retaining stumps of processes, so obtained are 90 percent pure and yield 33.6 x 10(6) cells per brain (3 milligrams, dry weight). The glial cells, apparently intact with extensive branched processess, are about 70 percent pure by weight and are obtained in a yield of 6.6 x 10(6) cells per brain (2 milligrams dry weight). The neurons are smaller and have less lipid than the glial cells.

摘要

经胰蛋白酶处理而软化的大鼠脑碎块,通过尼龙网和钢网过滤使其分散,以产生游离漂浮细胞和碎片的悬浮液。通过在不连续蔗糖梯度上离心来分离和纯化细胞。如此获得的带有突起残端的神经元胞体制剂纯度为90%,每只脑可产生33.6×10⁶个细胞(干重3毫克)。胶质细胞显然完整且有广泛的分支突起,按重量计纯度约为70%,每只脑的产量为6.6×10⁶个细胞(干重2毫克)。神经元比胶质细胞小且脂质含量少。

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