The etiology of neurodegenerative diseases such as Alzheimer's disease (AD) and Parkinson?s disease (PD) is heterogeneous, and epidemiological and laboratory studies suggest exposures to environmental toxins as a putative risk factor triggering the processes ultimately resulting in a neurodegenerative disease. Protein misfolding and aggregation are key common pathological features of these diseases. The accumulation of ?- synuclein (?Syn) aggregates is the hallmark of PD, while abnormal hyperphosphorylation of tau and the accumulation of tau aggregates in the neuronal fibrillary tangles are classically the most dominant etiologic features of AD?s pathology. Chronic exposure to high concentrations of manganese (Mn) results in adverse neurological health effects commonly referred to as manganism, an extrapyramidal disorder characterized by motor disturbances and neuropsychiatric and cognitive disabilities similar to Parkinsonism. While investigating the effects of Mn on ?Syn misfolding and cell-to-cell transfer, pursuant to the objective of our original parent grant award, we unexpectedly discovered that Mn promotes hyperphosphorylation of tau at pathological sites in brain regions associated with Mn-induced motor and cognitive deficits. Interestingly, the phosphorylated tau colocalized with PKC?, suggesting that PKC? kinase may hyperphosphorylate tau. Even though direct ?Syn- tau interactions have been suggested to be neurodegenerative, the precise role of environmental Mn exposure in the development of tau pathology and propagation and subsequent cognitive deficits is still not understood. Thus, this supplemental proposal addressing AD and its related dementias (ADRD) will further characterize the cellular and molecular mechanisms of Mn-induced tau pathology and exosomal transmission and its role in cognitive deficits. Our proposal will test the novel hypothesis that Mn exposure promotes the PKC?-dependent hyperphosphorylation of the microtubule-associated tau protein and that Mn also promotes the propagation of tau pathology between cells via exosomes, contributing to cognitive impairment and the neurodegenerative processes underlying environmentally linked AD and ADRD. Specific objectives of the proposal are i) to determine tau hyperphosphorylation and exosomal release in cell and animal models of Mn neurotoxicity and to characterize the role of PKC? and ?Syn during this Mn insult, and ii) to confirm the presence of Mn (plus other metals) and hyperphosphorylated tau in human brain and CSF samples and to validate exosomal tau release in those samples. Our proposed studies will offer novel insights into the role of environmental metal exposure in the propagation of misfolded tau pathology and its relevance to the etiology of AD and ADRD- associated cognitive deficits.

Public Health Relevance

Protein aggregation is a hallmark of many neurodegenerative diseases including Alzheimer's disease (AD) and Parkinson?s disease (PD), and metal exposure and Mn dyshomeostasis have been linked to protein aggregation and cognitive deficits in these disorders. However, the mechanisms by which Mn exposure modulates tau hyperphosphorylation and cell-to-cell transmission, as well as the precise molecular mechanisms in these processes have yet to be identified. Our proposal aims to characterize the effect of Mn exposure on the development and propagation of tau pathology to advance our understanding of the role environmental chemical exposure plays in the etiology of AD and its related dementias.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Research Project (R01)
Project #
3R01ES026892-03S1
Application #
9718597
Study Section
Program Officer
Hollander, Jonathan
Project Start
2016-06-01
Project End
2021-05-31
Budget Start
2018-09-07
Budget End
2019-05-31
Support Year
3
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Iowa State University
Department
Veterinary Sciences
Type
Schools of Veterinary Medicine
DUNS #
005309844
City
Ames
State
IA
Country
United States
Zip Code
50011
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