Synaptic Activity Reduces Intraneuronal Aβ, Promotes APP Transport to Synapses, and Protects against Aβ-Related Synaptic Alterations
Year: 2009
Type: article
Abstract: A central question in Alzheimer's disease research is what role synaptic activity plays in the disease process. Synaptic activity has been shown to induce beta-amyloid peptide release into the extracellular space, and extracellular beta-amyloid has been shown to be toxic to synapses. We now provide evidence that the well established synaptotoxicity of extracellular beta-amyloid requires gamma-secretase processing of amyloid precursor protein. Recent evidence supports an important role for intraneuronal beta-amyloid in the pathogenesis of Alzheimer's disease. We show that synaptic activity reduces intraneuronal beta-amyloid and protects against beta-amyloid-related synaptic alterations. We demonstrate that synaptic activity promotes the transport of the amyloid precursor protein to synapses using live cell imaging, and that the protease neprilysin is involved in reduction of intraneuronal beta-amyloid with synaptic activity.
Source: Journal of Neuroscience
Language: English
Subfield: Physiology
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
Awards: Intraneuronal Abeta accumulation: mechanism of pathogenesis, G1431933605, Mitochondrial Dysfunction in Alzheimer's Disease, The Subcellular Neuropathology of Alzheimer's Disease, BIOLOGY OF ALZHEIMER AMYLOID IN NEURONS, G380826963, G5672075673, G6273627651, Signaling Transduction and Alzheimer's Disease, G8365684821
OpenAlex ID: W2094929105
