Unraveling the Superficial White Matter of the Primate Brain: Tracer-Based Histology and dMRI Tractography Validation
Project Number5R01NS125307-03
Former Number1R01NS125307-01
Contact PI/Project LeaderRUSHMORE, RICHARD JARRETT Other PIs
Awardee OrganizationBOSTON UNIVERSITY MEDICAL CAMPUS
Description
Abstract Text
Abstract
In this 5 year R01 grant entitled “Unraveling the superficial white matter of the primate brain: Tracer-based
histology and diffusion MRI tractography validation,” we will map superficial white matter (SWM) in the primate
cerebrum using experimental tract tracing methods. We will use this ground truth information to validate high-
resolution in vivo and ultra-high resolution ex vivo diffusion MRI (dMRI) based tractography in the same rhesus
macaque monkeys. The SWM is a continuous layer located between the cerebral cortex of the forebrain and the
underlying white matter association pathways. It comprises axons that interconnect cerebral cortical areas,
including U-shaped fibers (U-fibers) under the cerebral sulci. This axonal layer plays a role in a broad range of
neurological conditions such as autism spectrum disorder, multiple sclerosis, and Alzheimer’s disease, and
knowledge of the SWM is essential for accurately interpreting dMRI-based tractography. Critically, the
fundamental connectional neuroanatomy of the SWM is largely unknown due to our inability to visualize the
specific origins, terminations, and trajectories of axons in the human brain. Our knowledge of human SWM
connectional neuroanatomy is thus derived almost exclusively from experimental tract tracing results in the non-
human primate (NHP) model, but comprehensive studies of the NHP SWM, from origin through trajectory to
termination, have not been performed. Therefore, knowledge of human SWM connectivity and organization can
be improved by invasive tract tracing studies in the NHP. The goal of the proposed research is to carry out the
first detailed neuroanatomical study of the SWM in the NHP brain, with dMRI validation in the NHP and translation
to human brains. To achieve this goal, we will use a range of histological techniques in conjunction with dMRI
scans obtained with the Massachusetts General Hospital (MGH) Connectom scanner to produce superior quality
dMRI data. We will first datamine the research literature to produce a compendium of existing knowledge of
SWM connectivity in the rhesus monkey. We will also examine the Pandya-Rosene Archive, a vast collection of
neuroanatomy cases that has formed the foundation of data on white matter connections in the NHP. We will
utilize this archive to chart the organization of the SWM in frontal brain areas. We will then use modern
histological methods, including CLARITY-based tissue clearing and neuroanatomical tract tracing, to interrogate
the structure, topography, and connectivity of the SWM, and thereby produce ground truth data. We will perform
in vivo and ex vivo dMRI in the same animals in which we perform neuroanatomical tract tracing experiments,
allowing for direct comparisons between histological and neuroimaging-based connectivity. Moreover, we will
disseminate the dMRI data to the neuroimaging community and host a competition to determine the optimal
tractography method for SWM. Finally, we will translate knowledge of SWM neuroanatomy to the human brain
using homologically based comparisons with Human Connectome Project datasets. These data will provide
ground truth of SWM connectivity and serve to improve dMRI tractography in NHP and human brains.
Public Health Relevance Statement
NARRATIVE
We propose the first validated and detailed study of the superficial white matter (SWM) in the non-human primate
brain using neuroanatomical tracers and diffusion MRI based tractography in the same experimental animals.
The SWM is a layer of axons underneath the cerebral cortex that connects different brain areas and is affected
in neurological diseases such as autism spectrum disorder and Alzheimer’s disease, but there is scant direct
knowledge of SWM organization and connectivity. Results will elucidate the SWM fiber systems in the non-
human primate brain with translational relevance to the human brain in health and disease.
NIH Spending Category
No NIH Spending Category available.
Project Terms
3-DimensionalAffectAlzheimer's DiseaseAnatomyAnimal ExperimentsAnimalsAntibodiesArchivesAreaAutopsyAxonBrainCellsCerebral cortexCerebral sulcusCerebrumCollectionCommunitiesComplementDataData SetDiffusion Magnetic Resonance ImagingDiseaseFeedbackFiberFoundationsGeneral HospitalsGoalsGrantHeadHealthHistologicHistological TechniquesHistologyHumanKnowledgeLabelLiteratureLocationMRI ScansMacacaMacaca mulattaMagnetic Resonance ImagingMapsMassachusettsMethodsModelingModernizationMonkeysMotorMotor CortexMultiple SclerosisNervous System DisorderNeuroanatomyNeurologicPathway interactionsPrecentral gyrusPrimatesProsencephalonReportingResearchResolutionScanningShapesSlideSomatosensory CortexSourceStructureSystemTimeTissuesTracerTranslatingValidationVisualizationWorkautism spectrum disorderchronic traumatic encephalopathyconnectomedata miningdata qualitydensitydesignex vivo imagingexperimental studyhuman diseaseimprovedin vivomillimeterneuralneuroimagingnonhuman primatenovelorganizational structuresystematic reviewtractographytranslation to humansultra high resolutionwhite matter
National Institute of Neurological Disorders and Stroke
CFDA Code
853
DUNS Number
604483045
UEI
FBYMGMHW4X95
Project Start Date
01-July-2022
Project End Date
30-June-2027
Budget Start Date
01-July-2024
Budget End Date
30-June-2025
Project Funding Information for 2024
Total Funding
$655,055
Direct Costs
$530,373
Indirect Costs
$124,682
Year
Funding IC
FY Total Cost by IC
2024
National Institute of Neurological Disorders and Stroke
$655,055
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 5R01NS125307-03
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
No Publications available for 5R01NS125307-03
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The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
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Clinical Studies
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History
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