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Neuroinflammatory TNF alpha Impairs Memory via Astrocyte Signaling

机译:神经炎性TNFα通过星形胶质细胞信号传导损害记忆。

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摘要

The occurrence of cognitive disturbances upon CNS inflammation or infection has been correlated with increased levels of the cytokine tumor necrosis factor-alpha (TNF alpha). To date, however, no specific mechanism via which this cytokine could alter cognitive circuits has been demonstrated. Here, we show that local increase of TNF alpha in the hippocampal dentate gyrus activates astrocyte TNF receptor type 1 (TNFR1), which in turn triggers an astrocyte-neuron signaling cascade that results in persistent functional modification of hippocampal excitatory synapses. Astrocytic TNFR1 signaling is necessary for the hippocampal synaptic alteration and contextual learning-memory impairment observed in experimental autoimmune encephalitis (EAE), an animal model of multiple sclerosis (MS). This process may contribute to the pathogenesis of cognitive disturbances in MS, as well as in other CNS conditions accompanied by inflammatory states or infections.
机译:中枢神经系统炎症或感染后认知障碍的发生与细胞因子肿瘤坏死因子-α(TNFα)水平升高相关。然而,迄今为止,尚未证明该细胞因子可通过其改变认知回路的具体机制。在这里,我们显示,海马齿状回中TNFα的局部增加会激活星形胶质细胞TNF受体1型(TNFR1),进而触发星形胶质细胞-神经元信号级联反应,从而导致海马兴奋性突触的持续功能修饰。在实验性自身免疫性脑炎(EAE)(一种多发性硬化症(MS)的动物模型)中观察到的海马突触改变和情境学习记忆障碍,星形胶质细胞TNFR1信号是必需的。此过程可能导致MS以及其他伴有炎症或感染的中枢神经系统疾病的认知障碍。

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