Center for Learning and Memory, The University of Texas at Austin, TX, USA.
Neuroscience. 2013 Oct 22;251:75-89. doi: 10.1016/j.neuroscience.2012.04.061. Epub 2012 May 1.
Because dendritic spines are the sites of excitatory synapses, pathological changes in spine morphology should be considered as part of pathological changes in neuronal circuitry in the forms of synaptic connections and connectivity strength. In the past, spine pathology has usually been measured by changes in their number or shape. A more complete understanding of spine pathology requires visualization at the nanometer level to analyze how the changes in number and size affect their presynaptic partners and associated astrocytic processes, as well as organelles and other intracellular structures. Currently, serial section electron microscopy (ssEM) offers the best approach to address this issue because of its ability to image the volume of brain tissue at the nanometer resolution. Renewed interest in ssEM has led to recent technological advances in imaging techniques and improvements in computational tools indispensable for three-dimensional analyses of brain tissue volumes. Here we consider the small but growing literature that has used ssEM analysis to unravel ultrastructural changes in neuropil including dendritic spines. These findings have implications in altered synaptic connectivity and cell biological processes involved in neuropathology, and serve as anatomical substrates for understanding changes in network activity that may underlie clinical symptoms.
由于树突棘是兴奋性突触的部位,因此应将其形态的病理性变化视为突触连接和连接强度形式的神经元回路病理性变化的一部分。过去,通常通过其数量或形状的变化来测量棘突病理学。更全面地了解棘突病理学需要在纳米级水平进行可视化,以分析数量和大小的变化如何影响其突触前伴侣和相关星形胶质细胞过程,以及细胞器和其他细胞内结构。目前,连续切片电子显微镜 (ssEM) 是解决此问题的最佳方法,因为它能够以纳米分辨率对脑组织体积进行成像。对 ssEM 的重新关注导致了成像技术的最新技术进步,以及对脑组织体积三维分析必不可少的计算工具的改进。在这里,我们考虑了一小部分但不断增长的文献,这些文献使用 ssEM 分析来揭示神经突起包括树突棘在内的超微结构变化。这些发现对改变的突触连接和涉及神经病理学的细胞生物学过程具有重要意义,并作为理解可能是临床症状基础的网络活动变化的解剖学基础。