Tau Pathology Induces Excitatory Neuron Loss, Grid Cell Dysfunction, and Spatial Memory Deficits Reminiscent of Early Alzheimer's Disease

被引:178
|
作者
Fu, Hongjun [1 ]
Rodriguez, Gustavo A. [1 ]
Herman, Mathieu [1 ]
Emrani, Sheina [1 ]
Nahmani, Eden [1 ]
Barrett, Geoffrey [1 ]
Figueroa, Helen Y. [1 ]
Goldberg, Eliana [1 ]
Hussaini, S. Abid [1 ,2 ]
Duff, Karen E. [1 ,2 ,3 ]
机构
[1] Columbia Univ, Med Ctr, Taub Inst Res Alzheimers Dis & Aging Brain, New York, NY 10032 USA
[2] Columbia Univ, Med Ctr, Dept Pathol & Cell Biol, New York, NY 10032 USA
[3] New York State Psychiat Inst & Hosp, Dept Integrat Neurosci, New York, NY 10032 USA
关键词
ENTORHINAL CORTEX; EEG DYNAMICS; MOUSE MODEL; LAYER-II; REPRESENTATION; NAVIGATION; NETWORK; STAGE; CA1; MAP;
D O I
10.1016/j.neuron.2016.12.023
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The earliest stages of Alzheimer's disease (AD) are characterized by the formation of mature tangles in the entorhinal cortex and disorientation and confusion when navigating familiar places. The medial entorhinal cortex (MEC) contains specialized neurons called grid cells that form part of the spatial navigation system. Here we show in a transgenic mouse model expressing mutant human tau predominantly in the EC that the formation of mature tangles in old mice was associated with excitatory cell loss and deficits in grid cell function, including destabilized grid fields and reduced firing rates, as well as altered network activity. Overt tau pathology in the aged mice was accompanied by spatial memory deficits. Therefore, tau pathology initiated in the entorhinal cortex could lead to deficits in grid cell firing and underlie the deterioration of spatial cognition seen in human AD.
引用
收藏
页码:533 / +
页数:14
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