Willis Dianna E, Twiss Jeffery L
Department of Biology, Drexel University, Philadelphia, PA, USA.
Methods Mol Biol. 2011;714:335-52. doi: 10.1007/978-1-61779-005-8_21.
The importance of mRNA localization and localized protein synthesis to spatially modulate protein levels in distinct subcellular domains has increasingly been recognized in recent years. Axonal and dendritic processes of neurons represent separate functional domains of the cell that have shown the capacity to autonomously respond to extracellular stimuli through localized protein synthesis. With the vast distance often separating distal axons and dendrites from the neuronal cell body, these processes have provided an appealing and useful model system to study the mechanisms that drive mRNA localization and regulate localized mRNA translation. Here, we discuss the methodologies that have been used to isolate neuronal processes to purity, and provide an in-depth method for using a modified Boyden chamber to isolate axons from adult dorsal root ganglion neurons for analyses of axonal mRNA content. We further show how this method can be utilized to identify specific mRNAs whose transport into axons is altered in response to extracellular stimuli, providing a means to begin to understand how axonal protein synthesis contributes to the proper function of the neuron.
近年来,信使核糖核酸(mRNA)定位和局部蛋白质合成在空间上调节不同亚细胞结构域中蛋白质水平的重要性日益得到认可。神经元的轴突和树突过程代表了细胞的不同功能结构域,它们已显示出通过局部蛋白质合成自主响应细胞外刺激的能力。由于远端轴突和树突通常与神经元细胞体相隔很远的距离,这些过程为研究驱动mRNA定位和调节局部mRNA翻译的机制提供了一个有吸引力且有用的模型系统。在这里,我们讨论了用于将神经元过程分离至纯度的方法,并提供了一种深入的方法,即使用改良的博伊登小室从成年背根神经节神经元中分离轴突,以分析轴突mRNA含量。我们进一步展示了如何利用该方法鉴定特定的mRNA,其向轴突的转运因细胞外刺激而改变,这为开始理解轴突蛋白质合成如何促进神经元的正常功能提供了一种手段。