Impairments of spatial memory in an Alzheimer's disease model via degeneration of hippocampal cholinergic synapses. Issue 1 (December 2017)

• Record Type: Journal Article
• Authors: Zhu, Houze; Yan, Huanhuan; Tang, Na; Li, Xinyan; Pang, Pei; Li, Hao; Chen, Wenting; Guo, Yu; Shu, Shu; Cai, You; Pei, Lei; Liu, Dan; Luo, Min-Hua; Man, Hengye; Tian, Qing; Mu, Yangling; Zhu, Ling-Qiang; Lu, Youming
• Is Part Of: Nature communications. Volume 8:Issue 1(2017)
• Page Start: 1
• Page End: 13
• Publication Date: 2017-12
• Subjects: Biology -- Periodicals; Physical sciences -- Periodicals; 505
• DOI: 10.1038/s41467-017-01943-0
• Languages: English
• ISSNs: 2041-1723

Abstract

Abstract 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. Cholinergic neurons in the diagonal band of Broca degenerate early in Alzheimer's disease. Here the authors show that in healthy mice, these cholinergic inputs innervate newborn neurons in the hippocampus, and that loss of this innervation in an Alzheimer's disease model leads to impairments in spatial memory.