Intra-Areal Visual Topography in Primate Brains Mapped with Probabilistic Tractography of Diffusion-Weighted Imaging

Author:

Tang-Wright K1,Smith J E T12,Bridge H3,Miller K L3,Dyrby T B45,Ahmed B1,Reislev N L4,Sallet J67ORCID,Parker A J189ORCID,Krug K18910ORCID

Affiliation:

1. Department of Physiology Anatomy and Genetics, University of Oxford, Oxford, OX1 3PT, UK

2. Ernst Strüngmann Institute (ESI) for Neuroscience in cooperation with Max Planck Society, 60528 Frankfurt, Germany

3. Wellcome Centre for Integrative Neuroimaging, FMRIB, Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford OX3 9DU, UK

4. Danish Research Centre for Magnetic Resonance, Centre for Functional and Diagnostic Imaging and Research, Copenhagen University Hospital, Amager & Hvidovre, 2650 Hvidovre, Denmark

5. Department of Applied Mathematics and Computer Science, Technical University of Denmark, 2800 Kongens Lyngby, Denmark

6. Wellcome Centre for Integrative Neuroimaging, Department of Experimental Psychology, University of Oxford, Oxford OX1 3UD, UK

7. Université Lyon 1, INSERM, Stem Cell and Brain Research Institute U1208, 69500 Bron, France

8. Institute of Biology, Otto-von-Guericke-University Magdeburg, 39120 Magdeburg, Germany

9. Leibniz Institute for Neurobiology, 39118 Magdeburg, Germany

10. Centre for Behavioral Brain Sciences, Otto-von-Guericke-University Magdeburg, 39106 Magdeburg, Germany

Abstract

Abstract Noninvasive diffusion-weighted magnetic resonance imaging (dMRI) can be used to map the neural connectivity between distinct areas in the intact brain, but the standard resolution achieved fundamentally limits the sensitivity of such maps. We investigated the sensitivity and specificity of high-resolution postmortem dMRI and probabilistic tractography in rhesus macaque brains to produce retinotopic maps of the lateral geniculate nucleus (LGN) and extrastriate cortical visual area V5/MT based on their topographic connections with the previously established functional retinotopic map of primary visual cortex (V1). We also replicated the differential connectivity of magnocellular and parvocellular LGN compartments with V1 across visual field positions. Predicted topographic maps based on dMRI data largely matched the established retinotopy of both LGN and V5/MT. Furthermore, tractography based on in vivo dMRI data from the same macaque brains acquired at standard field strength (3T) yielded comparable topographic maps in many cases. We conclude that tractography based on dMRI is sensitive enough to reveal the intrinsic organization of ordered connections between topographically organized neural structures and their resultant functional organization.

Funder

Biotechnology and Biological Sciences Research Council

Wellcome Trust Strategic Award

Deutsche Forschungsgemeinschaft

Sir Henry Dale Wellcome Trust Fellowship

Lundbeck Foundation

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience

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