TNFα in synaptic function: switching gears

被引:197
作者
Santello, Mirko [1 ]
Volterra, Andrea [1 ]
机构
[1] Univ Lausanne, Dept Cell Biol & Morphol, CH-1005 Lausanne, Switzerland
基金
瑞士国家科学基金会;
关键词
cytokines; TNF alpha; synaptic transmission; glia; gliotransmission; inflammation; TUMOR-NECROSIS-FACTOR; LONG-TERM POTENTIATION; KINASE-DEPENDENT MECHANISM; PERIPHERAL-NERVE INJURY; ALZHEIMERS-DISEASE; INFLAMMATORY CYTOKINES; AMPA-RECEPTOR; GLUTAMATE EXOCYTOSIS; NEURONAL-ACTIVITY; IMMUNE-RESPONSES;
D O I
10.1016/j.tins.2012.06.001
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Pathological brain states are known to induce massive production of proinflammatory cytokines, including tumor necrosis factor alpha (TNF alpha). At much lower levels, these cytokines are also present in the healthy brain, where it is increasingly being recognized that they exert regulatory influences. Recent studies suggest that TNF alpha plays important roles in controlling synaptic transmission and plasticity. Here, we discuss the evidence in support of synaptic regulation by TNF alpha and the underlying cellular mechanisms, including control of AMPA receptor trafficking and glutamate release from astrocytes. These findings suggest that increases in TNF alpha levels (caused by nervous system infection, injury, or disease) transform the physiological actions of the cytokine into deleterious ones. This functional switch may contribute to cognitive alterations in several brain pathologies.
引用
收藏
页码:638 / 647
页数:10
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