| Literature DB >> 26335643 |
Yingjun Zhao1, I-Chu Tseng2, Charles J Heyser3, Edward Rockenstein3, Michael Mante3, Anthony Adame3, Qiuyang Zheng1, Timothy Huang2, Xin Wang4, Pharhad E Arslan5, Paramita Chakrabarty6, Chengbiao Wu3, Guojun Bu4, William C Mobley3, Yun-Wu Zhang1, Peter St George-Hyslop7, Eliezer Masliah8, Paul Fraser9, Huaxi Xu10.
Abstract
Progressive supranuclear palsy (PSP) is a movement disorder characterized by tau neuropathology where the underlying mechanism is unknown. An SNP (rs1768208 C/T) has been identified as a strong risk factor for PSP. Here, we identified a much higher T-allele occurrence and increased levels of the pro-apoptotic protein appoptosin in PSP patients. Elevations in appoptosin correlate with activated caspase-3 and caspase-cleaved tau levels. Appoptosin overexpression increased caspase-mediated tau cleavage, tau aggregation, and synaptic dysfunction, whereas appoptosin deficiency reduced tau cleavage and aggregation. Appoptosin transduction impaired multiple motor functions and exacerbated neuropathology in tau-transgenic mice in a manner dependent on caspase-3 and tau. Increased appoptosin and caspase-3-cleaved tau were also observed in brain samples of patients with Alzheimer's disease and frontotemporal dementia with tau inclusions. Our findings reveal a novel role for appoptosin in neurological disorders with tau neuropathology, linking caspase-3-mediated tau cleavage to synaptic dysfunction and behavioral/motor defects.Entities:
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Year: 2015 PMID: 26335643 PMCID: PMC4575284 DOI: 10.1016/j.neuron.2015.08.020
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173