Human pyramidal cell study in primary visual and associative temporal cortex reveals key morphological features responsible for areal specializations

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Human pyramidal cell study in primary visual and associative temporal cortex reveals key morphological features responsible for areal specializations

Authors

Benavides Piccione, R.; Blazquez-Llorca, L.; Kastanauskaite, A.; Fernaud-Espinosa, I.; Gonzalez-Tapia, S.; DeFelipe, J.

Abstract

The basic building block of the cerebral cortex, the pyramidal cell, has been shown to be characterized by a markedly different dendritic structure among layers, cortical areas, and species. Functionally, differences in the structure of their dendrites and axons are critical in determining how neurons integrate information. However, within the human cortex, the pyramidal dendritic and axonal morphology has not been quantified in detail. In the present work, we performed intracellular injections of Lucifer Yellow and 3D reconstructed from confocal microscopy images over 200 pyramidal cells, including apical and basal dendritic and local axonal arbors and spines, from human occipital primary visual area (Brodmann area 17) and associative temporal cortex (Brodmann area 20 and 21). We found that human pyramidal neurons from BA20 and BA21 were larger, displayed more complex apical and basal structural organization and had more spines compared to those in primary visual cortex BA17. Moreover, these human neocortical cells displayed specific shared and distinct characteristics in comparison to previously published human hippocampal (CA1 field) pyramidal neurons. Additionally, we identified distinct morphological features in human cells that set them apart from mouse cells. Lastly, we observed certain consistent organizational patterns that are shared across species. This study emphasizes the existing diversity within pyramidal cell structures across different cortical areas and species, suggesting substantial species-specific variations in the computational properties of pyramidal cells.

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