Purpose: Recent studies indicate that T in white matter (WM) is influenced by fiber orientation in B . The purpose of the study was to investigate the interrelationships between axon fiber orientation in corpus callosum (CC) and T relaxation time in humans in vivo as well as in rat brain ex vivo.
Methods: Volunteers were scanned for relaxometric and diffusion MRI at 3 T and 7 T. Angular T plots from WM were computed using fractional anisotropy and fiber-to-field-angle maps. T and fiber-to-field angle were measured in five sections of CC to estimate the effects of inherently varying fiber orientations on T within the same tracts in vivo. Ex vivo rat-brain preparation encompassing posterior CC was rotated in B and T , and diffusion MRI images acquired at 9.4 T. T angular plots were determined at several rotation angles in B .
Results: Angular T plots from global WM provided reference for estimated fiber orientation-linked T changes within CC. In anterior midbody of CC in vivo, where small axons are dominantly present, a shift in axon orientation is accompanied by a change in T , matching that estimated from WM T data. In CC, where large and giant axons are numerous, the measured T change is about 2-fold greater than the estimated one. Ex vivo rotation of the same midsagittal CC region of interest produced angular T plots at 9.4 T, matching those observed at 7 T in vivo.
Conclusion: These data causally link axon fiber orientation in B to the T relaxation anisotropy in WM.
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http://dx.doi.org/10.1002/mrm.29667 | DOI Listing |
PLoS One
January 2025
Department of Life Science and Medical Bioscience, Laboratory of Cytoskeletal Logistics, Graduate School of Advanced Science and Engineering, Waseda University, Shinjuku, Tokyo, Japan.
In mammalian epithelial cells, cytoplasmic microtubules are mainly non-centrosomal, through the functions of the minus-end binding proteins CAMSAP2 and CAMSAP3. When cells enter mitosis, cytoplasmic microtubules are reorganized into the spindle composed of both centrosomal and non-centrosomal microtubules. The function of the CAMSAP proteins upon spindle assembly remains unknown, as these do not exhibit evident localization to spindle microtubules.
View Article and Find Full Text PDFAlzheimers Dement
December 2024
Michigan Alzheimer's Disease Research Center, Ann Arbor, MI, USA.
Background: Diffusion magnetic resonance imaging (dMRI) permits characterizing differences in white matter microstructure associated with amnestic mild cognitive impairment (aMCI) and Alzheimer's dementia (AD). However, most dMRI measures aggregate signals across multiple axonal fiber populations with varying spatial orientations, which limits the sensitivity and specificity of clinical diagnosis. To overcome this shortcoming, we estimated fiber density (FD) measures, independently from crossing fiber populations, and extracellular cerebral spinal fluid (CSF).
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View Article and Find Full Text PDFAlzheimers Dement
December 2024
Imaging Genetics Center, Mark and Mary Stevens Neuroimaging & Informatics Institute, University of Southern California, Marina del Rey, CA, USA.
Background: Along-tract analysis of white matter (WM) bundles can help map detailed patterns of WM pathway degeneration in Alzheimer's disease. Here, we present Medial Tractography Analysis (MeTA), which aims to minimize partial voluming and microstructural heterogeneity in diffusion MRI (dMRI) metrics by extracting and parcellating the volume along the bundle length while preserving bundle shape and capturing variation within and along WM bundles. We evaluated along-tract WM microstructure associations with clinical measures in ADNI using MeTA.
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