Lovell Peter, Jezzini Sami H, Moroz Leonid L
The Whitney Laboratory for Marine Bioscience, University of Florida, 9005 Ocean Shore Blvd., St. Augustine, FL 32080, USA.
J Neurosci Methods. 2006 Mar 15;151(2):114-20. doi: 10.1016/j.jneumeth.2005.06.030. Epub 2005 Sep 19.
Specific labeling of individual neurons and neuronal processes is virtually an everyday task for neuroscientists. Many traditional ways for delivery of intracellular dyes have limitations in terms of speed, efficiency and reproducibility. Electroporation is a fast, reliable and efficient method to deliver microscopic amounts of polar and charged molecules into neurons and their compartments such as individual neurites and growth cones. Here, we present a simple and highly effective procedure for intracellular labeling of individual Aplysia neurons both in intact ganglia and in cell culture. Pleural mechanoreceptor neurons have been used as illustrative examples to demonstrate applicability of direct and local labeling of the smallest individual neurites (< 2 microm) and single growth cones. Specifically, a 3-s train of 1.0 V hyperpolarizing pulses at 50 Hz effectively filled discrete neurites in contact with the tip of the micropipette with no dye transfer visible to other, non-contacted neurites. Application of this localized dye labeling technique to single neurites reveals a surprisingly complex morphology for patterns of axonal branching in culture. The protocol can be easily applied to a variety of models in neuroscience including accessible nervous systems of invertebrate animals.
对单个神经元和神经突起进行特异性标记,实际上是神经科学家的日常工作。许多传统的细胞内染料递送方法在速度、效率和可重复性方面都存在局限性。电穿孔是一种快速、可靠且高效的方法,可将微量的极性和带电分子递送至神经元及其各个部分,如单个神经突和生长锥。在此,我们展示了一种简单且高效的程序,用于在完整神经节和细胞培养中对单个海兔神经元进行细胞内标记。胸膜机械感受器神经元已被用作示例,以证明对最小的单个神经突(<2微米)和单个生长锥进行直接和局部标记的适用性。具体而言,以50Hz施加一串持续3秒、1.0V的超极化脉冲,有效地使与微吸管尖端接触的离散神经突充满染料,而其他未接触的神经突未见染料转移。将这种局部染料标记技术应用于单个神经突,揭示了培养中轴突分支模式令人惊讶的复杂形态。该方案可轻松应用于神经科学的各种模型,包括无脊椎动物易于研究神经系统。