Hamam Bassam N, Kennedy Timothy E
Centre for Neuronal Survival, Montreal Neurological Institute, McGill University, 3801 University St, Montreal, Quebec, Canada H3A 2B4.
J Neurosci Methods. 2003 Feb 15;123(1):61-7. doi: 10.1016/s0165-0270(02)00341-2.
Characterizing the structure and electrophysiological properties of single neurons is essential for understanding how individual cells contribute to the function of neuronal networks. Following intra-cellular recording from neurons in acute brain slices, the structure of the recorded cell has typically been examined by serial sectioning of the tissue slice and then reconstructing the neuron of interest; a labor-intensive and time-consuming process. Here, we have adapted a whole-mount immunohistochemical technique and used it to visualize the dendritic arbor of individual neurons in sections of adult CNS tissue up to 500 microm thick. Permeabilization of the slice and extensive washing allow histochemical reagents to penetrate and be washed from the section, producing limited background staining. Using this method, the cell within the slice can be sectioned optically and reconstructed using the optical sections. We present images of the dendritic trees of neurons in 500 microm thick slices of adult rat entorhinal cortex and hippocampus, labeled either immunohistochemically, or by biocytin injection following whole-cell patch clamp or sharp electrode recordings. The resolution obtained is sufficient to visualize dendritic spines deep within the section. The method is free from artifacts associated with cutting serial sections and is broadly applicable to tasks that require visualization of the fine structure of individual cells in thick slices of CNS tissue.
表征单个神经元的结构和电生理特性对于理解单个细胞如何对神经网络的功能发挥作用至关重要。在对急性脑片上的神经元进行细胞内记录后,通常通过对组织切片进行连续切片,然后重建感兴趣的神经元来检查记录细胞的结构;这是一个劳动强度大且耗时的过程。在这里,我们采用了一种整装免疫组织化学技术,并将其用于可视化成年中枢神经系统组织切片中单个神经元的树突分支,切片厚度可达500微米。切片的通透处理和充分洗涤使得组织化学试剂能够渗透并从切片中洗去,产生有限的背景染色。使用这种方法,可以对切片内的细胞进行光学切片,并利用光学切片进行重建。我们展示了成年大鼠内嗅皮质和海马体500微米厚切片中神经元树突树的图像,这些图像通过免疫组织化学标记,或者在全细胞膜片钳或尖锐电极记录后用生物胞素注射标记。获得的分辨率足以可视化切片深处的树突棘。该方法没有与连续切片相关的伪像,并且广泛适用于需要可视化中枢神经系统组织厚切片中单个细胞精细结构的任务。