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    Evaluating Proteinopathy and Consequences for Behavior in Animal Models of Human Neurodegenerative Disease

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    Author
    Bjork, Reed
    Issue Date
    2025
    Keywords
    alpha-synuclein
    drosophila
    neurodegeneration
    songbird
    TDP-43
    Advisor
    Miller, Julie
    
    Metadata
    Show full item record
    Publisher
    The University of Arizona.
    Rights
    Copyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction, presentation (such as public display or performance) of protected items is prohibited except with permission of the author.
    Abstract
    Neurodegenerative diseases such as Amyotrophic Lateral Sclerosis (ALS), Frontotemporal Dementia (FTD) and Parkinson’s Disease (PD) are devastating and incurable conditions associated with human aging that are rapidly growing in incidence and global economic burden. While these diseases of the central nervous system are complex, heterogeneous and multi-factorial in humans, experimental animal models based on the most common pathological predictors provide a framework for elucidating the cellular and molecular mechanisms leading to the progressive deterioration of behavior that largely characterizes these afflictions. Chapter 1 of this dissertation summarizes current literature outlining the characterization and pathophysiology of ALS, FTD and PD. Chapter 2 summarizes my contribution to novel work modeling FTD in fruit flies (Drosophila melanogaster) based on TDP-43 proteinopathy in mushroom body (MB) neurons. This work demonstrates a progressive thinning of MB lobes with resulting deficits in working memory, sleep and lifespan, and uncovers novel RNA targets of TDP-43 proteinopathy in MB neurons that are both unique and shared with targets identified in motor neurons within a fly model of ALS. Chapter 3 describes my most recent work in zebra finch songbirds evaluating the regional and subcellular distribution of alpha-synuclein (αsyn) neuropathy in the basal ganglia and the resulting effects on song behavior. This work establishes a novel tool, the Border Expression Ratio, for measuring locality and severity of αsyn neuropathy, revealing a positive correlation between right hemisphere pathology and a reduction in the variation of harmonic syllable duration. This work also revealed the detection of pSer129, a marker for pathologically aggregated αsyn typically enriched in Lewy bodies common to PD. Chapter 4 discusses the convergence of pathologies across neurodegenerative diseases, the limitations of these models and suggestions for future studies.
    Type
    text
    Electronic Dissertation
    Degree Name
    Ph.D.
    Degree Level
    doctoral
    Degree Program
    Graduate College
    Neuroscience
    Degree Grantor
    University of Arizona
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