O'Brien John, Lummis Sarah C R
Neurobiology Division, MRC Laboratory of Molecular Biology, Hills Road, Cambridge CB2 2QH, UK.
Methods. 2004 Jun;33(2):121-5. doi: 10.1016/j.ymeth.2003.11.010.
Delivery of genes by firing them into mammalian cells is becoming increasingly popular for cells such as neurones, that have proved difficult to transfect by conventional means. In addition it is becoming apparent that this technique also provides a suitable method of introducing cell-specific dyes into mammalian tissues. Here we describe improved protocols for the rapid and efficient delivery of both DNA and lipophilic dyes into mammalian cells in both monolayers and in brain slices. The results show that transfection of genes, such as that for enhanced yellow fluorescent protein, using a modified microcarrier preparation technique combined with either a conventional or novel accelerator channel, yields rapid and efficient production of protein, which can be visualised in 24-48 h. Following similar delivery of lipophilic dyes neurones can be visualised in minutes. These techniques therefore provide an excellent means not only to examine the structure and function of neurones and neuronal genes, but also those of other cell types.
通过将基因射入哺乳动物细胞来实现基因传递,对于诸如神经元这类传统方法难以转染的细胞而言,正变得越来越流行。此外,越来越明显的是,这项技术还提供了一种将细胞特异性染料引入哺乳动物组织的合适方法。在此,我们描述了改进的方案,可将DNA和亲脂性染料快速高效地递送至单层培养的哺乳动物细胞以及脑片中的细胞。结果表明,使用改良的微载体制备技术结合传统或新型加速通道,转染诸如增强型黄色荧光蛋白基因,能快速高效地产生蛋白质,且在24至48小时内即可观察到。在进行类似的亲脂性染料递送后,数分钟内即可观察到神经元。因此,这些技术不仅提供了一种绝佳手段来研究神经元和神经元基因的结构与功能,还能用于研究其他细胞类型的结构与功能。