| Literature DB >> 26686654 |
Samia Habbas1, Mirko Santello1, Denise Becker1, Hiltrud Stubbe1, Giovanna Zappia1, Nicolas Liaudet1, Federica R Klaus2, George Kollias3, Adriano Fontana4, Christopher R Pryce2, Tobias Suter5, Andrea Volterra6.
Abstract
The occurrence of cognitive disturbances upon CNS inflammation or infection has been correlated with increased levels of the cytokine tumor necrosis factor-α (TNFα). To date, however, no specific mechanism via which this cytokine could alter cognitive circuits has been demonstrated. Here, we show that local increase of TNFα 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.Entities:
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Year: 2015 PMID: 26686654 DOI: 10.1016/j.cell.2015.11.023
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582