Document Type
Article
Publication Date
4-4-2007
Department
Chemistry and Biochemistry
School
Mathematics and Natural Sciences
Abstract
Neurofibrillary tangles (NFTs) are a pathological hallmark of Alzheimer's disease and other tauopathies, but recent studies in a conditional mouse model of tauopathy (rTg4510) have suggested that NFT formation can be dissociated from memory loss and neurodegeneration. This suggests that NFTs are not the major neurotoxic tau species, at least during the early stages of pathogenesis. To identify other neurotoxic tau protein species, we performed biochemical analyses on brain tissues from the rTg4510 mouse model and then correlated the levels of these tau proteins with memory loss. We describe the identification and characterization of two forms of tau multimers (140 and 170 kDa), whose molecular weight suggests an oligomeric aggregate, that accumulate early in the pathogenic cascade in this mouse model. Similar tau multimers were detected in a second mouse model of tauopathy (JNPL3) and in tissue from patients with Alzheimer's disease and FTDP-17 (frontotemporal dementia and parkinsonism linked to chromosome 17). Moreover, levels of the tau multimers correlated consistently with memory loss at various ages in the rTg4510 mouse model. Our findings suggest that accumulation of early-stage aggregated tau species, before the formation of NFT, is associated with the development of functional deficits during the pathogenic progression of tauopathy.
Publication Title
Journal of Neuroscience
Volume
27
Issue
14
First Page
3650
Last Page
3662
Recommended Citation
Berger, Z.,
Roder, H.,
Hanna, A.,
Rangachari, V.,
Yue, M.,
Wszolek, Z.,
Ashe, K.,
Knight, J.,
Dickson, D.,
Andorfer, C.,
Rosenberry, T. L.,
Lewis, J.,
Hutton, M.,
Janus, C.
(2007). Accumulation of Pathological Tau Species and Memory Loss in a Conditional Model of Tauopathy. Journal of Neuroscience, 27(14), 3650-3662.
Available at: https://aquila.usm.edu/fac_pubs/7541
Comments
Originally published in The Journal of Neuroscience, April 4, 2007; 27(14):3650 –3662