Neuronal activity regulates extracellular tau in vivo

被引:423
作者
Yamada, Kaoru [1 ]
Holth, Jerrah K. [1 ]
Liao, Fan [1 ]
Stewart, Floy R. [1 ]
Mahan, Thomas E. [1 ]
Jiang, Hong [1 ]
Cirrito, John R. [1 ]
Patel, Tirth K. [1 ]
Hochgraefe, Katja [2 ,3 ]
Mandelkow, Eva-Maria [2 ,3 ]
Holtzman, David M. [1 ]
机构
[1] Washington Univ, Sch Med, Knight Alzheimers Dis Res Ctr, Dept Neurol,Hope Ctr Neurol Disorders, St Louis, MO 63110 USA
[2] DZNE German Ctr Neurodegenerat Dis, D-53175 Bonn, Germany
[3] CAESAR Res Ctr, D-53175 Bonn, Germany
基金
日本学术振兴会;
关键词
ALZHEIMERS-DISEASE; ALPHA-SYNUCLEIN; PROPAGATION; MODEL; TRANSMISSION; AGGREGATION; PATHOLOGY; RELEASE;
D O I
10.1084/jem.20131685
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Tau is primarily a cytoplasmic protein that stabilizes microtubules. However, it is also found in the extracellular space of the brain at appreciable concentrations. Although its presence there may be relevant to the intercellular spread of tau pathology, the cellular mechanisms regulating tau release into the extracellular space are not well understood. To test this in the context of neuronal networks in vivo, we used in vivo microdialysis. Increasing neuronal activity rapidly increased the steady-state levels of extracellular tau in vivo. Importantly, presynaptic glutamate release is sufficient to drive tau release. Although tau release occurred within hours in response to neuronal activity, the elimination rate of tau from the extracellular compartment and the brain is slow (half-life of similar to 11 d). The in vivo results provide one mechanism underlying neuronal tau release and may link trans-synaptic spread of tau pathology with synaptic activity itself.
引用
收藏
页码:387 / 393
页数:7
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