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Lipid Metabolism Influence on Neurodegenerative Disease Progression: Is the Vehicle as Important as the Cargo?

Journal

FRONTIERS IN MOLECULAR NEUROSCIENCE
Volume 14, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fnmol.2021.788695

Keywords

lipid metabolism; protein aggregation and propagation; extracellular vesicle; Parkinson's disease; Alzheimer's disease; glia; glucocerebrosidase (GBA); ceramide

Categories

Funding

  1. Veterans Administration Office of Research and Development
  2. Biomedical Laboratory Research and Development [IK2 BX003244, R01 NS119897]
  3. University of Washington Institute for Stem Cell and Regenerative Medicine

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The pathogenesis of neurodegenerative diseases involves both the formation of pathogenic protein aggregates and their spread throughout the nervous system. Alterations in lipid metabolism and dysregulation of extracellular vesicles are considered key factors accelerating the spread of protein aggregation and disease progression.
Many neurodegenerative diseases are characterized by abnormal protein aggregates, including the two most common neurodegenerative diseases Alzheimer's disease (AD) and Parkinson's disease (PD). In the global search to prevent and treat diseases, most research has been focused on the early stages of the diseases, including how these pathogenic protein aggregates are initially formed. We argue, however, that an equally important aspect of disease etiology is the characteristic spread of protein aggregates throughout the nervous system, a key process in disease progression. Growing evidence suggests that both alterations in lipid metabolism and dysregulation of extracellular vesicles (EVs) accelerate the spread of protein aggregation and progression of neurodegeneration, both in neurons and potentially in surrounding glia. We will review how these two pathways are intertwined and accelerate the progression of AD and PD. Understanding how lipid metabolism, EV biogenesis, and EV uptake regulate the spread of pathogenic protein aggregation could reveal novel therapeutic targets to slow or halt neurodegenerative disease progression.

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