陶氏病
神经科学
神经退行性变
细胞外
新皮层
细胞内
生物
病态的
运动前神经元活动
疾病
细胞生物学
医学
病理
作者
Noa Menkes-Caspi,Hagar G. Yamin,Vered Kellner,Tara L. Spires‐Jones,Dana Cohen,Edward A. Stern
出处
期刊:Neuron
[Elsevier]
日期:2015-03-01
卷期号:85 (5): 959-966
被引量:154
标识
DOI:10.1016/j.neuron.2015.01.025
摘要
Summary
Pathological tau leads to dementia and neurodegeneration in tauopathies, including Alzheimer's disease. It has been shown to disrupt cellular and synaptic functions, yet its effects on the function of the intact neocortical network remain unknown. Using in vivo intracellular and extracellular recordings, we measured ongoing activity of neocortical pyramidal cells during various arousal states in the rTg4510 mouse model of tauopathy, prior to significant cell death, when only a fraction of the neurons show pathological tau. In transgenic mice, membrane potential oscillations are slower during slow-wave sleep and under anesthesia. Intracellular recordings revealed that these changes are due to longer Down states and state transitions of membrane potentials. Firing rates of transgenic neurons are reduced, and firing patterns within Up states are altered, with longer latencies and inter-spike intervals. By changing the activity patterns of a subpopulation of affected neurons, pathological tau reduces the activity of the neocortical network.
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