Impairments of spatial memory in an Alzheimer’s disease model via degeneration of hippocampal cholinergic synapses

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作者
Houze Zhu
Huanhuan Yan
Na Tang
Xinyan Li
Pei Pang
Hao Li
Wenting Chen
Yu Guo
Shu Shu
You Cai
Lei Pei
Dan Liu
Min-Hua Luo
Hengye Man
Qing Tian
Yangling Mu
Ling-Qiang Zhu
Youming Lu
机构
[1] Huazhong University of Science and Technology,Department of Physiology, School of Basic Medicine and Tongji Medical College
[2] Huazhong University of Science and Technology,The Institute for Brain Research, Collaborative Innovation Center for Brain Science
[3] Huazhong University of Science and Technology,Department of Neurobiology, School of Basic Medicine and Tongji Medical College
[4] Huazhong University of Science and Technology,Department of Genetics, School of Basic Medicine and Tongji Medical College
[5] Chinese Academy of Sciences,State Key Laboratory of Virology, CAS Center for Excellence in Brain Science and Intelligence Technology (CEBSIT), Wuhan Institute of Virology
[6] Boston University,Department of Biology
[7] Huazhong University of Science and Technology,Department of Pathophysiology, School of Basic Medicine and Tongji Medical College
来源
Nature Communications | / 8卷
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摘要
Choline acetyltransferase neurons in the vertical diagonal band of Broca (vChATs) degenerate in the early stage of Alzheimer’s disease (AD). Here, we report that vChATs directly innervate newly generated immature neurons (NGIs) in the dorsal hippocampus (dNGIs) of adult mice and regulate both the dNGIs survival and spatial pattern separation. In a mouse model that exhibits amyloid-β plaques similar to AD patients, cholinergic synaptic transmission, dNGI survival and spatial pattern separation are impaired. Activation of vChATs with theta burst stimulation (TBS) that alleviates the decay in cholinergic synaptic transmission effectively protects against spatial pattern separation impairments in the AD mice and this protection was completely abolished by inhibiting the dNGIs survival. Thus, the impairments of pattern separation-associated spatial memory in AD mice are in part caused by degeneration of cholinergic synaptic transmission that modulates the dNGIs survival.
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