Briggman Kevin L, Denk Winfried
Max-Planck Institute for Medical Research, Jahnstrasse 29,69120 Heidelberg, Germany.
Curr Opin Neurobiol. 2006 Oct;16(5):562-70. doi: 10.1016/j.conb.2006.08.010. Epub 2006 Sep 8.
Electron microscopy is the only currently available technique with a resolution adequate to identify and follow every axon and dendrite in dense neuropil. Reconstructions of large volumes of neural tissue, necessary to reconstruct even local neural circuits, have, however, been inhibited by the daunting task of serially sectioning and reconstructing thousands of sections. Recent technological developments have improved the quality of volume electron microscopy data and automated its acquisition. This opens up the prospect of reconstructing almost complete invertebrate and sizable fractions of vertebrate nervous systems. Such reconstructions of complete neural wiring diagrams could rekindle the tradition of relating neural function to the underlying neuroanatomical circuitry.
电子显微镜是目前唯一分辨率足以识别并追踪密集神经毡中每一根轴突和树突的技术。然而,即使是重建局部神经回路所必需的大量神经组织的重建工作,也因连续切片和重建数千个切片这一艰巨任务而受到阻碍。最近的技术发展提高了体电子显微镜数据的质量并实现了其采集自动化。这为重建几乎完整的无脊椎动物神经系统以及相当一部分脊椎动物神经系统开辟了前景。对完整神经布线图的此类重建可能会重新唤起将神经功能与潜在神经解剖回路联系起来的传统。