Accumulation of proteinaceous aggregates is one of the defining hallmarks of neurodegenerative diseases. How these proteins cause disease and how they are subsequently cleared has remained an enigma. Tau, a microtubule binding protein, is one such aggregated protein found in multiple neurodegenerative syndromes including Frontotemporal dementia (FTD), Alzheimer's disease (AD), Progressive Supranuclear Palsy (PSP), and Corticobasalganglionic Degeneration (CBD). Understanding tau mediated neurodegeneration may lead to important therapeutic strategies for these disorders. Our goal is to study how decreasing tau levels and decreasing 4R:3R tau ratios affects the behavioral and pathological abnormalities in mouse models of dementia. Previous studies demonstrate that tau knockout animals are protected from amyloid beta induced behavioral abnormalities in mice. Our goal is to test whether decreasing mouse tau in older animals will also provide protection. Some mutations in tau that cause FTD lead to changes in alternative splicing and increased levels of 4R:3R tau. An N279K FTD mouse model replicates the splicing defect and behavioral pathological changes. Our goal is to test whether reversing the splicing defect in an adult N279K can reverse the behavioral and pathologic changes. In order to decrease tau mRNA and protein levels, we will infuse antisense oligonucleotides into the cerebral spinal fluid that bathes the brain and spinal cord. These oligos activate RNAse H and degrade tau mRNA. To decrease 4R:3R tau ratios, we will use a similar antisense oligo strategy, but with antisense oligos designed to promote exclusion of exon 10 (and thus decrease 4R:3R ratio) rather than decreasing tau mRNA. We show preliminary evidence for a set of oligos that decrease tau mRNA in vitro and for another group of oligos that decrease 4R:3R ratios in vitro. After establishing the efficacy of these oligos following intraventricular infusion, we will treat J20 APP mice with oligos that decrease mouse tau mRNA and protein and treat N279K tau mice with oligos that decrease 4R:3R ratios by changing tau splicing. We anticipate that these oligos will prevent the behavioral and pathological changes seen in these models. These data would form the basis for a similar treatment strategy in patients.

Public Health Relevance

There are no treatments which substantially delay the progression of Alzheimer's disease or Frontotemporal dementia. This proposal tests whether changing a protein called tau will improve behavior and pathological changes in mouse models of Alzheimer's disease and Frontotemporal dementia. This novel therapeutic strategy, if successful would be applicable to human dementias.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Specialized Center (P50)
Project #
5P50AG005681-30
Application #
8459491
Study Section
Special Emphasis Panel (ZAG1-ZIJ-4)
Project Start
Project End
Budget Start
2013-05-01
Budget End
2014-04-30
Support Year
30
Fiscal Year
2013
Total Cost
$189,241
Indirect Cost
$64,502
Name
Washington University
Department
Type
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Su, Yi; Blazey, Tyler M; Snyder, Abraham Z et al. (2015) Partial volume correction in quantitative amyloid imaging. Neuroimage 107:55-64
Shim, Yong Soo; Yang, Dong-Won; Roe, Catherine M et al. (2015) Pathological correlates of white matter hyperintensities on magnetic resonance imaging. Dement Geriatr Cogn Disord 39:92-104
Wang, Li-San; Naj, Adam C; Graham, Robert R et al. (2015) Rarity of the Alzheimer disease-protective APP A673T variant in the United States. JAMA Neurol 72:209-16
Karch, Celeste M; Goate, Alison M (2015) Alzheimer's disease risk genes and mechanisms of disease pathogenesis. Biol Psychiatry 77:43-51
Ghoshal, Nupur; Perry, Arie; McKeel, Daniel et al. (2015) Variably Protease-sensitive Prionopathy in an Apparent Cognitively Normal 93-Year-Old. Alzheimer Dis Assoc Disord 29:173-6
Hurth, Kyle; Tarawneh, Rawan; Ghoshal, Nupur et al. (2015) Whipple's disease masquerades as dementia with Lewy bodies. Alzheimer Dis Assoc Disord 29:85-9
Aschenbrenner, Andrew J; Balota, David A; Tse, Chi-Shing et al. (2015) Alzheimer disease biomarkers, attentional control, and semantic memory retrieval: Synergistic and mediational effects of biomarkers on a sensitive cognitive measure in non-demented older adults. Neuropsychology 29:368-81
Benitez, Bruno A; Jin, Sheng Chih; Guerreiro, Rita et al. (2014) Missense variant in TREML2 protects against Alzheimer's disease. Neurobiol Aging 35:1510.e19-26
Dobrowolska, Justyna A; Kasten, Tom; Huang, Yafei et al. (2014) Diurnal patterns of soluble amyloid precursor protein metabolites in the human central nervous system. PLoS One 9:e89998
Hetland, Amanda J; Carr, David B; Wallendorf, Michael J et al. (2014) Potentially driver-impairing (PDI) medication use in medically impaired adults referred for driving evaluation. Ann Pharmacother 48:476-82

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