| Literature DB >> 30266683 |
Jing-Yi Liu1, Xiao-Xin Chen1, Hai-Yong Chen1, Jun Shi1, George Pak-Heng Leung2, Sydney Chi-Wai Tang3, Li-Xing Lao1, Henry Ka-Fun Yip4, Kai-Fai Lee5, Stephen Cho-Wing Sze6, Zhang-Jin Zhang7, Kalin Yanbo Zhang8.
Abstract
Alzheimer's disease (AD) is the most common cause of dementia in the elderly, characterized by progressive cognitive dysfunction. Aquaporin 9 (AQP9) is an aquaglyceroporin membrane channel shown biophysically to conduct water, glycerol, and other small solutes. In our study, we reported for the first time an age-associated decrease in AQP9 mRNA and protein expressions in both hippocampus and cerebral cortex of APPswe/PS1dE9 (Tg) AD mice at 3, 6 and 10 months of age. Consistently, we observed a dose-dependent downregulation of AQP9 expression in PC12 cells after treatment with amyloid-beta protein 1-40 (Aβ1-40). Pre-treatment with AQP9 small interfering RNA led to a more severe neurotoxicity in PC12 cells in response to Aβ1-40. Furthermore, we corroborated that the active participation of AQP9 in AD progression is associated with Aβ-induced apoptosis both in vitro and in vivo. Taken together, our results reveal an important role of AQP9 in Aβ-induced pathogenesis of AD which deserves further investigation.Entities:
Keywords: APPswe/PS1dE9; Alzheimer's disease; apoptosis; aquaporin 9; beta-amyloid
Mesh:
Substances:
Year: 2018 PMID: 30266683 DOI: 10.1016/j.neuroscience.2018.09.016
Source DB: PubMed Journal: Neuroscience ISSN: 0306-4522 Impact factor: 3.590