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使用腺病毒载体将基因快速导入培养的海马神经元和急性海马脑片中。

Rapid gene transfer into cultured hippocampal neurons and acute hippocampal slices using adenoviral vectors.

作者信息

Griesbeck O, Korte M, Gravel C, Bonhoeffer T, Thoenen H

机构信息

Abteilung Neurochemie, Max-Planck-Institut für Psychiatrie, Martinsried, Germany.

出版信息

Brain Res Mol Brain Res. 1997 Feb;44(1):171-7. doi: 10.1016/s0169-328x(96)00246-x.

Abstract

Primary cultures of hippocampal neurons were infected with an adenovirus coding for beta-galactosidase. Expression could be detected as early as 4 h after infection and steadily increased to high levels at 24 h without evidence for a functional impairment of the infected neurons. Similarly, adenovirus-mediated gene transfer into acute hippocampal slices was detectable 4 h after infection and could be localized to discrete areas of the CA1 region by microinjection of the virus stock solution. Infected slices were still suitable for electrophysiological experiments.

摘要

海马神经元原代培养物用编码β-半乳糖苷酶的腺病毒进行感染。感染后4小时即可检测到表达,并且在24小时时稳定增加至高水平,而未发现被感染神经元有功能受损的迹象。同样,感染后4小时可检测到腺病毒介导的基因转移进入急性海马脑片,并且通过微量注射病毒储备液可将其定位到CA1区的离散区域。被感染的脑片仍适用于电生理实验。

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