0000000000372559

AUTHOR

Kengo Uemura

showing 1 related works from this author

Neuronal activity and secreted amyloid β lead to altered amyloid β precursor protein and presenilin 1 interactions.

2013

Deposition of amyloid β (Aβ) containing plaques in the brain is one of the neuropathological hallmarks of Alzheimer's disease (AD). It has been suggested that modulation of neuronal activity may alter Aβ production in the brain. We postulate that these changes in Aβ production are due to changes in the rate-limiting step of Aβ generation, APP cleavage by γ-secretase. By combining biochemical approaches with fluorescence lifetime imaging microscopy, we found that neuronal inhibition decreases endogenous APP and PS1 interactions, which correlates with reduced Aβ production. By contrast, neuronal activation had a two-phase effect: it initially enhanced APP-PS1 interaction leading to increased …

ImmunoprecipitationBlotting WesternEndogenyMice TransgenicCleavage (embryo)PresenilinArticlelcsh:RC321-571Amyloid beta-Protein PrecursorMiceAlzheimer Diseasemental disordersmedicinePresenilin-1Premovement neuronal activityAnimalsHumansImmunoprecipitationlcsh:Neurosciences. Biological psychiatry. NeuropsychiatryFeedback PhysiologicalNeuronsPresenilin 1Neuronal activityAmyloid beta-PeptidesChemistryP3 peptideNeurotoxicityAlzheimer's diseasemedicine.diseaseImmunohistochemistryCell biologyNeurologyBiochemistrynervous systemAlzheimer's diseaseAmyloid β precursor proteinFLIM (fluorescence lifetime imaging microscopy)Neurobiology of disease
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