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The role of ryanodine receptor type 3 in a mouse model of Alzheimer disease
Authors:Jie Liu  Charlene Supnet  Suya Sun  Hua Zhang  Levi Good  Elena Popugaeva  Ilya Bezprozvanny
Affiliation:1.Department of Physiology; University of Texas Southwestern Medical Center Dallas; Dallas, TX USA;2.Department of Neurology and Neurotherapeutics; University of Texas Southwestern Medical Center Dallas; Dallas, TX USA;3.Laboratory of Molecular Neurodegeneration (LMN); St. Petersburg State Polytechnical University; St. Petersburg, Russia
Abstract:Dysregulated endoplasmic reticulum (ER) calcium (Ca2+) signaling is reported to play an important role in Alzheimer disease (AD) pathogenesis. The role of ER Ca2+ release channels, the ryanodine receptors (RyanRs), has been extensively studied in AD models and RyanR expression and activity are upregulated in the brains of various familial AD (FAD) models. The objective of this study was to utilize a genetic approach to evaluate the importance of RyanR type 3 (RyanR3) in the context of AD pathology.
Keywords:ryanodine receptor   Arc   spontaneous activity   amyloid load   spine morphology   EEG   caffeine
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