Maladaptive cortical hyperactivity upon recovery from experimental autoimmune encephalomyelitis. (October 2018)

• Record Type: Journal Article
• Authors: Ellwardt, Erik; Pramanik, Gautam; Luchtman, Dirk; Novkovic, Tanja; Jubal, Eduardo; Vogt, Johannes; Arnoux, Isabelle; Vogelaar, Christina; Mandal, Shibajee; Schmalz, Melanie; Barger, Zeke; Ruiz de Azua, Inigo; Kuhlmann, Tanja; Lutz, Beat; Mittmann, Thomas; Bittner, Stefan; Zipp, Frauke; Stroh, Albrecht
• Is Part Of: Nature neuroscience. Volume 21:Number 10(2018)
• Page Start: 1392
• Page End: 1403
• Publication Date: 2018-10
• Subjects: Neurosciences -- Periodicals; 573.8
• DOI: 10.1038/s41593-018-0193-2
• Languages: English
• ISSNs: 1097-6256

Abstract

Abstract Multiple sclerosis (MS) patients exhibit neuropsychological symptoms in early disease despite the immune attack occurring predominantly in white matter and spinal cord. It is unclear why neurodegeneration may start early in the disease and is prominent in later stages. We assessed cortical microcircuit activity by employing spiking-specific two-photon Ca2+ imaging in proteolipid protein-immunized relapsing-remitting SJL/J mice in vivo. We identified the emergence of hyperactive cortical neurons in remission only, independent of direct immune-mediated damage and paralleled by elevated anxiety. High levels of neuronal activity were accompanied by increased caspase-3 expression. Cortical TNFα expression was mainly increased by excitatory neurons in remission; blockade with intraventricular infliximab restored AMPA spontaneous excitatory postsynaptic current frequencies, completely recovered normal neuronal network activity patterns and alleviated elevated anxiety. This suggests a dysregulation of cortical networks attempting to achieve functional compensation by synaptic plasticity mechanisms, indicating a link between immune attack and early start of neurodegeneration. The authors report TNFα-dependent hyperactivity in cortical microcircuits during remission in a mouse model of multiple sclerosis, a maladaptive response to the immune attack with behavioral changes.