| Home > Publications Database > Oligodendrocytes produce amyloid-β and contribute to plaque formation alongside neurons in Alzheimer's disease model mice. |
| Journal Article | DZNE-2024-01102 |
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2024
Nature America
New York, NY
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Please use a persistent id in citations: doi:10.1038/s41593-024-01730-3
Abstract: Amyloid-β (Aβ) is thought to be neuronally derived in Alzheimer's disease (AD). However, transcripts of amyloid precursor protein (APP) and amyloidogenic enzymes are equally abundant in oligodendrocytes (OLs). By cell-type-specific deletion of Bace1 in a humanized knock-in AD model, APPNLGF, we demonstrate that OLs and neurons contribute to Aβ plaque burden. For rapid plaque seeding, excitatory projection neurons must provide a threshold level of Aβ. Ultimately, our findings are relevant for AD prevention and therapeutic strategies.
Keyword(s): Animals (MeSH) ; Alzheimer Disease: metabolism (MeSH) ; Alzheimer Disease: pathology (MeSH) ; Alzheimer Disease: genetics (MeSH) ; Neurons: metabolism (MeSH) ; Neurons: pathology (MeSH) ; Oligodendroglia: metabolism (MeSH) ; Oligodendroglia: pathology (MeSH) ; Amyloid beta-Peptides: metabolism (MeSH) ; Disease Models, Animal (MeSH) ; Plaque, Amyloid: pathology (MeSH) ; Plaque, Amyloid: metabolism (MeSH) ; Amyloid Precursor Protein Secretases: metabolism (MeSH) ; Mice (MeSH) ; Mice, Transgenic (MeSH) ; Aspartic Acid Endopeptidases: metabolism (MeSH) ; Humans (MeSH) ; Amyloid beta-Protein Precursor: metabolism (MeSH) ; Amyloid beta-Protein Precursor: genetics (MeSH) ; Amyloid beta-Peptides ; Amyloid Precursor Protein Secretases ; Aspartic Acid Endopeptidases ; Amyloid beta-Protein Precursor ; Bace1 protein, mouse
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