Department of Physiology, School of Basic Medicine and Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 4030030, China.
The Institute for Brain Research, Collaborative Innovation Center for Brain Science, Huazhong University of Science and Technology, Wuhan, 430030, China.
Nat Commun. 2017 Nov 22;8(1):1676. doi: 10.1038/s41467-017-01943-0.
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.
在阿尔茨海默病(AD)的早期阶段,布罗卡垂直对角带中的胆碱乙酰转移酶神经元(vChATs)会退化。在这里,我们报告 vChATs 直接支配成年小鼠背侧海马(dNGIs)中新生的未成熟神经元(NGIs),并调节 dNGIs 的存活和空间模式分离。在一种表现出类似于 AD 患者的淀粉样β斑块的小鼠模型中,胆碱能突触传递、dNGI 的存活和空间模式分离受损。通过 theta 爆发刺激(TBS)激活 vChATs,有效地缓解胆碱能突触传递的衰减,可有效防止 AD 小鼠的空间模式分离障碍,而通过抑制 dNGIs 的存活,这种保护作用则完全被消除。因此,AD 小鼠的与模式分离相关的空间记忆障碍部分是由调节 dNGIs 存活的胆碱能突触传递退化引起的。