Malinow Roberto, Hayashi Yasunori, Maletic-Savatic Mirjana, Zaman Shahid H, Poncer Jean-Christophe, Shi Song-Hai, Esteban José A, Osten Pavel, Seidenman Ken
Cold Spring Harb Protoc. 2010 Apr;2010(4):pdb.prot5406. doi: 10.1101/pdb.prot5406.
Expression of green fluorescent protein (GFP), its more fluorescent mutant forms (e.g., EGFP [enhanced GFP]), or their fusion protein derivatives, affords a number of informative possibilities in cellular neuroscience. EGFP is a soluble protein and appears to be homogeneously distributed within the cytosol of neurons when expressed. Thus, it reveals the structure of the neuron, including the cell body, and axonal and dendritic arbors. It is also sufficiently bright to reveal detailed structures such as axonal boutons and dendritic spines. When expressed as a fusion protein, EGFP can provide information about the distribution characteristics of the proteins within neurons. Furthermore, during single-cell electrophysiological studies, such expression can direct the investigator to record from a cell carrying a foreign gene. In this protocol, we describe the use of the Sindbis pseudovirus expression system to deliver GFP to neurons. Sindbis is a member of the alphaviruses, which are plus-stranded RNA viruses. This protocol uses the DH(26S) strain, which preferentially infects neurons over glia (50:1). Two infection methods are given: one for dissociated hippocampal cultured neurons and one for organotypic hippocampal slices.
绿色荧光蛋白(GFP)、其荧光更强的突变形式(如增强型绿色荧光蛋白[EGFP])或它们的融合蛋白衍生物的表达,在细胞神经科学中提供了许多有用的可能性。EGFP是一种可溶性蛋白,表达时似乎均匀分布在神经元的胞质溶胶中。因此,它揭示了神经元的结构,包括细胞体、轴突和树突分支。它也足够亮,能够揭示诸如轴突终扣和树突棘等详细结构。当作为融合蛋白表达时,EGFP可以提供有关蛋白质在神经元内分布特征的信息。此外,在单细胞电生理研究中,这种表达可以指导研究人员从携带外源基因的细胞中进行记录。在本实验方案中,我们描述了使用辛德毕斯假病毒表达系统将GFP递送至神经元。辛德毕斯是甲病毒属的成员,属于正链RNA病毒。本实验方案使用DH(26S)毒株,它优先感染神经元而非胶质细胞(比例为50:1)。给出了两种感染方法:一种用于解离的海马培养神经元,另一种用于海马脑片培养。