The meso-connectomes of mouse, marmoset, and macaque: network organization and the emergence of higher cognition

Loïc Magrou, Mary Kate P Joyce, Sean Froudist-Walsh, Dibyadeep Datta, Xiao-Jing Wang, Julio Martinez-Trujillo, Amy F T Arnsten*

*Corresponding author for this work

Research output: Contribution to journalArticle (Academic Journal)peer-review

1 Citation (Scopus)

Abstract

The recent publications of the inter-areal connectomes for mouse, marmoset, and macaque cortex have allowed deeper comparisons across rodent vs. primate cortical organization. In general, these show that the mouse has very widespread, “all-to-all” inter-areal connectivity (i.e. a “highly dense” connectome in a graph theoretical framework), while primates have a more modular organization. In this review, we highlight the relevance of these differences to function, including the example of primary visual cortex (V1) which, in the mouse, is interconnected with all other areas, therefore including other primary sensory and frontal areas. We argue that this dense inter-areal connectivity benefits multimodal associations, at the cost of reduced functional segregation. Conversely, primates have expanded cortices with a modular connectivity structure, where V1 is almost exclusively interconnected with other visual cortices, themselves organized in relatively segregated streams, and hierarchically higher cortical areas such as prefrontal cortex provide top–down regulation for specifying precise information for working memory storage and manipulation. Increased complexity in cytoarchitecture, connectivity, dendritic spine density, and receptor expression additionally reveal a sharper hierarchical organization in primate cortex. Together, we argue that these primate specializations permit separable deconstruction and selective reconstruction of representations, which is essential to higher cognition.
Original languageEnglish
Article numberbhae174
Number of pages27
JournalCerebral Cortex
Volume34
Issue number5
DOIs
Publication statusPublished - 20 May 2024

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© The Author(s) 2024.

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