Hyperphosphorylated tau in parahippocampal cortex impairs place learning in aged mice expressing wild-type human tau

被引:118
作者
Kimura, Tetsuya [1 ]
Yamashita, Shunji [1 ]
Fukuda, Tetsuya [1 ]
Park, Jun-Mi [1 ]
Murayama, Miyuki [1 ]
Mizoroki, Tatsuya [1 ]
Yoshiike, Yuji [1 ]
Sahara, Naruhiko [1 ]
Takashima, Akihiko [1 ]
机构
[1] RIKEN, Brain Sci Inst, Alzheimers Res Lab, Wako, Saitama 3510198, Japan
关键词
aging; learning and memory; Mn-enhanced MRI; tau phosphorylation; transgenic mouse;
D O I
10.1038/sj.emboj.7601917
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To investigate how tau affects neuronal function during neurofibrillary tangle (NFT) formation, we examined the behavior, neural activity, and neuropathology of mice expressing wild-type human tau. Here, we demonstrate that aged (420 months old) mice display impaired place learning and memory, even though they do not form NFTs or display neuronal loss. However, soluble hyperphosphorylated tau and synapse loss were found in the same regions. Mn-enhanced MRI showed that the activity of the parahippocampal area is strongly correlated with the decline of memory as assessed by the Morris water maze. Taken together, the accumulation of hyperphosphorylated tau and synapse loss in aged mice, leading to inhibition of neural activity in parahippocampal areas, including the entorhinal cortex, may underlie place learning impairment. Thus, the accumulation of hyperphosphorylated tau that occurs before NFT formation in entorhinal cortex may contribute to the memory problems seen in Alzheimer's disease (AD).
引用
收藏
页码:5143 / 5152
页数:10
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