Where Do Core Thalamocortical Axons Terminate in Mammalian Neocortex When There Is No Cytoarchitecturally Distinct Layer 4?

Author:

Bhagwandin Adhil1,Molnár Zoltán2ORCID,Bertelsen Mads F.3,Karlsson Karl Æ.4,Alagaili Abdulaziz N.5,Bennett Nigel C.6,Hof Patrick R.7,Kaswera‐Kyamakya Consolate8,Gilissen Emmanuel910,Jayakumar Jaikishan1112,Manger Paul R.1ORCID

Affiliation:

1. School of Anatomical Sciences, Faculty of Health Sciences University of the Witwatersrand Johannesburg Republic of South Africa

2. Department of Physiology, Anatomy and Genetics Sherrington Building, University of Oxford Oxford UK

3. Centre for Zoo and Wild Animal Health, Copenhagen Zoo Frederiksberg Denmark

4. Biomedical Engineering Reykjavik University Reykjavik Iceland

5. Department of Zoology King Saud University Riyadh Saudi Arabia

6. South African Research Chair of Mammal Behavioural Ecology and Physiology University of Pretoria Pretoria South Africa

7. Nash Family Department of Neuroscience, Center for Discovery and Innovation, and Friedman Brain Institute Icahn School of Medicine at Mount Sinai New York New York USA

8. Faculté des Sciences University of Kisangani Kisangani People's Republic of Congo

9. Department of African Zoology Royal Museum for Central Africa Tervuren Belgium

10. Laboratory of Histology and Neuropathology Université Libre de Bruxelles Brussels Belgium

11. Sudha Gopalakrishnan Brain Centre Indian Institute of Technology Madras Chennai India

12. Center for Computational Brain Research Indian Institute of Technology Madras Chennai India

Abstract

ABSTRACTAlthough the mammalian cerebral cortex is most often described as a hexalaminar structure, there are cortical areas (primary motor cortex) and species (elephants, cetaceans, and hippopotami), where a cytoarchitecturally indistinct, or absent, layer 4 is noted. Thalamocortical projections from the core, or first order, thalamic system terminate primarily in layers 4/inner 3. We explored the termination sites of core thalamocortical projections in cortical areas and in species where there is no cytoarchitecturally distinct layer 4 using the immunolocalization of vesicular glutamate transporter 2, a known marker of core thalamocortical axon terminals, in 31 mammal species spanning the eutherian radiation. Several variations from the canonical cortical column outline of layer 4 and core thalamocortical inputs were noted. In shrews/microchiropterans, layer 4 was present, but many core thalamocortical projections terminated in layer 1 in addition to layers 4 and inner 3. In primate primary visual cortex, the sublaminated layer 4 was associated with a specialized core thalamocortical projection pattern. In primate primary motor cortex, no cytoarchitecturally distinct layer 4 was evident and the core thalamocortical projections terminated throughout layer 3. In the African elephant, cetaceans, and river hippopotamus, no cytoarchitecturally distinct layer 4 was observed and core thalamocortical projections terminated primarily in inner layer 3 and less densely in outer layer 3. These findings are contextualized in terms of cortical processing, perception, and the evolutionary trajectory leading to an indistinct or absent cortical layer 4.

Publisher

Wiley

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