Wen Hua, Brehm Paul
Vollum Institute, Oregon Health and Sciences University, USA.
J Vis Exp. 2010 Nov 20(45):2351. doi: 10.3791/2351.
Larval zebrafish represent the first vertebrate model system to allow simultaneous patch clamp recording from a spinal motor-neuron and target muscle. This is a direct consequence of the accessibility to both cell types and ability to visually distinguish the single segmental CaP motor-neuron on the basis of morphology and location. This video demonstrates the microscopic methods used to identify a CaP motor-neuron and target muscle cells as well as the methodologies for recording from each cell type. Identification of the CaP motor-neuron type is confirmed by either dye filling or by the biophysical features such as action potential waveform and cell input resistance. Motor-neuron recordings routinely last for one hour permitting long-term recordings from multiple different target muscle cells. Control over the motor-neuron firing pattern enables measurements of the frequency-dependence of synaptic transmission at the neuromuscular junction. Owing to a large quantal size and the low noise provided by whole cell voltage clamp, all of the unitary events can be resolved in muscle. This feature permits study of basic synaptic properties such as release properties, vesicle recycling, as well as synaptic depression and facilitation. The advantages offered by this in vivo preparation eclipse previous neuromuscular model systems studied wherein the motor-neurons are usually stimulated by extracellular electrodes and the muscles are too large for whole cell patch clamp. The zebrafish preparation is amenable to combining electrophysiological analysis with a wide range of approaches including transgenic lines, morpholino knockdown, pharmacological intervention and in vivo imaging. These approaches, coupled with the growing number of neuromuscular disease models provided by mutant lines of zebrafish, open the door for new understanding of human neuromuscular disorders.
斑马鱼幼体是首个能够同时对脊髓运动神经元和靶肌肉进行膜片钳记录的脊椎动物模型系统。这直接得益于两种细胞类型都易于获取,以及能够根据形态和位置在视觉上区分单个节段性CaP运动神经元。本视频展示了用于识别CaP运动神经元和靶肌肉细胞的显微方法,以及从每种细胞类型进行记录的方法。通过染料填充或动作电位波形和细胞输入电阻等生物物理特征来确认CaP运动神经元类型。运动神经元记录通常持续一小时,允许对多个不同的靶肌肉细胞进行长期记录。对运动神经元放电模式的控制能够测量神经肌肉接头处突触传递的频率依赖性。由于量子大小较大且全细胞电压钳提供的噪声较低,肌肉中的所有单突触事件都可以分辨出来。这一特性允许研究基本的突触特性,如释放特性、囊泡循环以及突触抑制和易化。这种体内制备方法所具有的优势超越了以往研究的神经肌肉模型系统,在以往的系统中,运动神经元通常由细胞外电极刺激,而肌肉对于全细胞膜片钳来说太大了。斑马鱼制备方法适合将电生理分析与多种方法相结合,包括转基因品系、吗啉代敲低、药物干预和体内成像。这些方法,再加上斑马鱼突变品系提供的越来越多的神经肌肉疾病模型,为深入了解人类神经肌肉疾病打开了大门。