Cited by 437Extracellular vesicles in diseaseNeuroinflammation and Neurodegeneration MechanismsAlzheimer's disease research and treatments

Extracellular Vesicles and Neurodegenerative Diseases

Open access
Hill, Andrew F.·2019·The Journal of Neuroscience

Abstract

Extracellular vesicles (EVs) include exosomes and microvesicles and have been shown to have roles in the CNS ranging from the removal of unwanted biomolecules to intercellular communication to the spread of pathogenic proteins associated with neurodegenerative diseases. EVs carry protein, lipid, and genetic cargo, and research over more than a decade has shown that they contain the misfolded forms of proteins associated with Alzheimer's, Parkinson's, and the prion diseases. Altered genetic cargo, usually in the form of miRNAs, have also been identified in EVs patients with these diseases, suggesting that EVs may be a source of disease biomarkers. Whether EVs play a key role in the pathogenesis of neurological diseases remains to be firmly established because most current research is performed using cell culture and transgenic animal models. If EVs are identified as a key pathological contributor to neurological conditions, they will form a novel target for therapeutic intervention. This Dual Perspectives article will discuss the current understanding of the role of EVs in neurological diseases and raise some of the limitations of our current understandings of this field. Dual Perspectives Companion Paper: NeuroEVs: Characterizing Extracellular Vesicles Generated in the Neural Domain, by Christie D. Fowler

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Crossref · 10.1523/jneurosci.0147-18.2019

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6 of 6 references verified0 citation errors · 0 not checkable

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  • Neurodegenerative diseases, such as AD characterized by Aβ and tau accumulation, PD associated with α-synuclein aggregates, and ALS marked by SOD1 misfolding, are increasingly understood in the context of sEVs involvement.

    “Neurodegenerative diseases, such as AD characterized by Aβ and tau accumulation, PD associated with α-synuclein aggregates, and ALS marked by superoxide dismutase 1 (SOD 1) misfolding, are increasingly understood in the context of sEVs involvement [45, 113, 129].”

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Authors
Hill, A. F.
Affiliations
La Trobe University (AU)
Corresponding author
Hill, Andrew F.
Venue
The Journal of Neuroscience
Published
2019-11-20
Volume
39
Issue
47
Pages
9269-9273
ISSN
  • 0270-6474 (ISSN-L)
  • 1529-2401
OpenAlex
W2991169791
Cited by
437
References
6
Citations by year
2026: 42 · 2025: 66 · 2024: 79 · 2023: 84 · 2022: 87 · 2021: 52 · 2020: 26
FWCI
13.73
Type
journal article
Language
en
Open access
Locations
  • Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • Victoria University Research Repository (Victoria University) (submittedVersion)
  • Figshare (submittedVersion)
Funders
  • Medical Research Council
  • Australian Research Council (DP170102312)
  • National Health and Medical Research Council (1132604)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Extracellular vesicles in disease
  • Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
  • Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
Keywords
extracellular vesicles, exosomes, microvesicles, neurodegenerative diseases, Alzheimer's disease, Parkinson's disease, prion disease, protein misfolding, intercellular communication, microRNA, disease biomarkers, therapeutic target
MeSH terms
Extracellular Vesicles, Animals, Brain, Cell Communication, Humans, Neurodegenerative Diseases, Exosomes

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