突触素在体外神经元分化过程中的表达。免疫细胞化学和共聚焦激光显微研究。

P Sindou, P Couratier, D Barthe, C Yardin, J Hugon
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引用次数: 0

摘要

哺乳动物胎儿脑原代神经元培养广泛用于形态学、生化和药物毒理学研究。相对纯净的神经元培养物在这类研究中的作用现已得到证实。我们使用两种不同的培养基:含有10%胎牛血清的M1培养基和添加激素、离子和化学物质的M2培养基,比较了原代神经元培养中神经元的存活和分化、突触素表达和胶质细胞百分比。我们的研究表明,M2培养基(一种无血清的培养基)与培养14天的存活率增加、早期的神经元分化和细胞体和神经突中的突触素表达有关,免疫细胞化学和共聚焦激光显微镜研究证实了这一点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synaptophysin expression during in vitro neuronal differentiation. An immunocytochemical and a confocal laser microscopic study.

Primary neuronal cultures from mammalian fetal brains are widely used for morphological, biochemical and pharmacotoxicological studies. The usefulness of relatively pure neuronal cultures are now demonstrated for such studies. We have compared the neuronal survival and differentiation, the synaptophysin expression and the glial cell percentage in primary neuronal cultures using two different media: a M1 medium containing 10 % fetal calf serum and a M2 medium supplemented with hormones, ions and chemicals. Our study demonstrates that the M2 medium (a serum-free defined medium) is associated with an increased survival at 14 days of culture, an earlier neuronal differentiation and synaptophysin expression in cell bodies and neurites as it was confirmed by immunocytochemical and confocal laser microscopic studies.

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