Amyloid-β oligomers as a template for secondary amyloidosis in Alzheimer's disease
- M.J. Guerrero-Muñoz,
- ,
- S. Krishnamurthy,
- A.A. Paulucci-Holthauzen,
- U. Sengupta,
- C.A. Lasagna-Reeves
- University of Texas Medical Branch at Galveston
Research Output:
Contribution to journal
Article
Peer-reviewSustainable Development Goals
- SDG 3 Good Health and Well
Publication metrics
Metrics
SciVal
FWCI
1.68
SciVal
Author count
9
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Citations
65
SciVal
Paper percentile
83
Abstract
Alzheimer's disease is a complex disease characterized by overlapping phenotypes with different neurodegenerative disorders. Oligomers are considered the most toxic species in amyloid pathologies. We examined human AD brain samples using an anti-oligomer antibody generated in our laboratory and detected potential hybrid oligomers composed of amyloid-β, prion protein, α-synuclein, and TDP-43 phosphorylated at serines 409 and 410. These data and in vitro results suggest that Aβ oligomer seeds act as a template for the aggregation of other proteins and generate an overlapping phenotype with other neuronal disorders. Furthermore, these results could explain why anti-amyloid-β therapy has been unsuccessful.
Publication Information
Output type
Research Output:
Contribution to journal
Article
Peer-reviewOriginal language
EnglishPages from-to (Number of pages)
Pages 14-23 (10 pages)Journal (Volume, Issue Number)
Neurobiology of Disease (Volume 71)Publication milestones
- Published - 11/2014
Publication status
Published - 11/2014
ISSN
0969-9961Publication IDs
- ORCID: /0000-0003-2511-949X/work/43281173
- Scopus: 84906503278
- WOS: 000342549900002
