Axonal Transport Impairment and its Relationship with Diffusion Tensor Imaging Metrics of a Murine Model of p301L Tau Induced Tauopathy

• Published in: Neuroscience Vol. 498; pp. 144 - 154
• Main Authors: Nishioka, Christopher, Liang, Hsiao-Fang, Ong, Stephen, Sun, Shu-Wei
• Format: Journal Article
• Language: English
• Published: Elsevier Ltd 21.08.2022
• Subjects: Diffusion Tensor Imaging (DTI); Manganese Enhanced MRI (MEMRI); P301L mouse model; tauopathy; white matter; tauopathy; AD; ALS; T1WI; Diffusion Tensor Imaging (DTI); Manganese Enhanced MRI (MEMRI); SC; white matter; MEMRI; rD; P301L mouse model; mD; DTI; FA; ON
• ISSN: 0306-4522; 1873-7544; 1873-7544
• DOI: 10.1016/j.neuroscience.2022.06.025

•Correlation between MEMRI and DTI was found in P301L tau mice.•Axonal transport deficits in tauopathy were correlated with the loss of myelin.•Myelin loss may contribute to the axonal degeneration in tauopathy. Diffusion Tensor Imaging (DTI) and Manganese Enhanced MRI (MEMRI) are noninvasive tools to characterize neural fiber microstructure and axonal transport. A combination of both may provide novel insights into the progress of neurodegeneration. To investigate the relationship of DTI and MEMRI in white matter of tauopathy, twelve optic nerves of 11-month-old p301L tau mice were imaged and finished with postmortem immunohistochemistry. MEMRI was used to quantify Mn2+ accumulation rates in the optic nerve (ON, termed ONAR) and the Superior Colliculus (SC, termed SCAR), the primary terminal site of ON in mice. We found that both ONAR and SCAR revealed a significant linear correlation with mean diffusion (mD) and radial diffusion (rD) but not with other DTI quantities. Immunohistochemistry findings showed that ONAR, mD, and rD are significantly correlated with the myelin content (Myelin Basic Protein, p < 0.05) but not with the axonal density (SMI-31), tubulin density, or tau aggregates (AT8 staining). In summary, slower axonal transport appeared to have less myelinated axons and thinner remaining axons, associated with reduced rD and mD of in vivo DTI. A combination of in vivo MEMRI and DTI can provide critical information to delineate the progress of white matter deficits in neurodegenerative diseases.