Moriyoshi K, Richards L J, Akazawa C, O'Leary D D, Nakanishi S
Institute for Immunology Kyoto University Faculty of Medicine Kyoto.
Neuron. 1996 Feb;16(2):255-60. doi: 10.1016/s0896-6273(00)80044-6.
We describe an experimental system to visualize the soma and processes of mammalian neurons and glia in living and fixed preparations by using a recombinant adenovirus vector to transfer the jellyfish green fluorescent protein (GFP) into postmitotic neural cells both in vitro and in vivo. We have introduced several modifications of GFP that enhance its fluorescence intensity in mammalian axons and dendrites. This method should be useful for studying the dynamic processes of cell migration and the development of neuronal connections, as well as for analyzing the function of exogenous genes introduced into cells using the adenovirus vector.
我们描述了一种实验系统,通过使用重组腺病毒载体将水母绿色荧光蛋白(GFP)导入体外和体内有丝分裂后的神经细胞,从而在活体和固定标本中可视化哺乳动物神经元和神经胶质细胞的胞体及突起。我们对GFP进行了几种修饰,增强了其在哺乳动物轴突和树突中的荧光强度。该方法对于研究细胞迁移的动态过程和神经元连接的发育,以及分析使用腺病毒载体导入细胞的外源基因的功能应该是有用的。