Neuroanatomy and Global Neuroscience

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Neuroanatomy and Global Neuroscience Javier DeFelipe  Neuron  Volume 95, Issue 1, Pages 14-18 (July 2017) DOI: 10.1016/j.neuron.2017.05.027 Copyright © 2017 Elsevier Inc. Terms and Conditions

Figure 1 Theoretical Direction of Transmission of Impulses in Cortical Circuits Published by Cajal in 1894 (Middle Column) and Lorente de Nó in 1934 (Right Column) The diagrams stem from the neuron doctrine, the law of dynamic polarization of nerve cells and sparse anatomical data. Taken from DeFelipe (2014). Neuron 2017 95, 14-18DOI: (10.1016/j.neuron.2017.05.027) Copyright © 2017 Elsevier Inc. Terms and Conditions

Figure 2 Integration of Microanatomical Data Schematic representation to show how we could deal with the problem of imprecise connectomes and incomplete synaptomes focusing on the cortical columns. (A) Instead of reconstructing all cellular components within the column, the principles governing the structural design of cells can be obtained by using data from a few 3D-reconstructed neurons and applying mathematical tools to determine the statistical structure of the neurons to computationally synthesize model neurons. The cells can be labeled with markers that allow full visualization of their dendritic and axonal arbors and then 3D reconstructed at the light microscope level, allowing the morphometric analysis of individual cells (i.e., patterns of dendritic arbors, distribution and density of dendritic spines, etc.). These data are also critical for modeling neuronal functions such as synaptic integration in dendrites and dendritic spines. For instance, based on the dendritic spine distribution and their morphology (different colors represent different sizes), it is possible to generate maps of putative synaptic currents. (B) Another set of structural data comes from measurements of the gray matter thickness, the volume fraction of cortical elements (neuropil, neurons, glia, and blood vessels), and neuron and glia density per volume, together with the patterns of local (intralaminar, translaminar) and long-range (cortico-cortical, thalamo-cortical, cortico-thalamic, subcortical extra-thalamic) connections. To determine the synaptic contribution of pyramidal cells in a given cortical layer, it is impractical to reconstruct all of these cells at the electron-microscope level. Instead, this parameter could be inferred by combining quantitative light-microscopy data on the total number and microanatomical characteristics of these cells with the average density of axo-spinous and axo-dendritic synapses obtained by analyzing multiple samples of the 3D reconstructed neuropil using automated electron microscopy techniques and tools for image analysis, segmentation, and quantification of different types of synapses (green, asymmetric synapses; red, symmetric synapses). Neuron 2017 95, 14-18DOI: (10.1016/j.neuron.2017.05.027) Copyright © 2017 Elsevier Inc. Terms and Conditions