Zhao Yingjun, Tseng I-Chu, Heyser Charles J, Rockenstein Edward, Mante Michael, Adame Anthony, Zheng Qiuyang, Huang Timothy, Wang Xin, Arslan Pharhad E, Chakrabarty Paramita, Wu Chengbiao, Bu Guojun, Mobley William C, Zhang Yun-Wu, St George-Hyslop Peter, Masliah Eliezer, Fraser Paul, Xu Huaxi
Fujian Provincial Key Laboratory of Neurodegenerative Disease and Aging Research, Institute of Neuroscience, College of Medicine, Xiamen University, Xiamen, Fujian 361102, China; Degenerative Diseases Program, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA 92037, USA.
Degenerative Diseases Program, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA 92037, USA.
Neuron. 2015 Sep 2;87(5):963-75. doi: 10.1016/j.neuron.2015.08.020.
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.
进行性核上性麻痹(PSP)是一种以tau神经病理学为特征的运动障碍,其潜在机制尚不清楚。一种单核苷酸多态性(SNP,rs1768208 C/T)已被确定为PSP的一个强风险因素。在此,我们发现PSP患者中T等位基因的出现频率更高,且促凋亡蛋白凋亡素的水平升高。凋亡素水平的升高与活化的半胱天冬酶-3及半胱天冬酶切割的tau水平相关。凋亡素的过表达增加了半胱天冬酶介导的tau切割、tau聚集及突触功能障碍,而凋亡素缺乏则减少了tau切割及聚集。凋亡素转导以一种依赖于半胱天冬酶-3和tau的方式损害了tau转基因小鼠的多种运动功能并加剧了神经病理学变化。在患有阿尔茨海默病及伴有tau包涵体的额颞叶痴呆患者的脑样本中也观察到凋亡素及半胱天冬酶-3切割的tau增加。我们的研究结果揭示了凋亡素在伴有tau神经病理学的神经疾病中的新作用,将半胱天冬酶-3介导的tau切割与突触功能障碍及行为/运动缺陷联系起来。