Kainate receptor auxiliary subunit NETO2 is required for normal fear expression and extinction

• Published in: Neuropsychopharmacology (New York, N.Y.) Vol. 44; no. 11; pp. 1855 - 1866
• Main Authors: Mennesson, Marie, Rydgren, Emilie, Lipina, Tatiana, Sokolowska, Ewa, Kulesskaya, Natalia, Morello, Francesca, Ivakine, Evgueni, Voikar, Vootele, Risbrough, Victoria, Partanen, Juha, Hovatta, Iiris
• Format: Journal Article
• Language: English
• Published: England Nature Publishing Group 01.10.2019; Springer International Publishing
• Subjects: Amygdala; Amygdala - metabolism; Animals; Anxiety; Conditioning, Classical - physiology; Extinction behavior; Extinction, Psychological - physiology; Fear - physiology; Fear conditioning; Glutamic acid receptors; Hippocampus; Hippocampus - metabolism; Hybridization; Kainic acid receptors; Maze Learning - physiology; Membrane Proteins - genetics; Membrane Proteins - metabolism; Mental disorders; Mice; Mice, Knockout; Neurons - metabolism; Phenotypes; Post traumatic stress disorder; Prefrontal cortex; Prefrontal Cortex - metabolism; Receptors, N-Methyl-D-Aspartate - genetics; Receptors, N-Methyl-D-Aspartate - metabolism; Synapses; Synapses - metabolism; Synaptosomes - metabolism
• ISSN: 0893-133X; 1740-634X
• DOI: 10.1038/s41386-019-0344-5

NETO1 and NETO2 are auxiliary subunits of kainate receptors (KARs). They interact with native KAR subunits to modulate multiple aspects of receptor function. Variation in KAR genes has been associated with psychiatric disorders in humans, and in mice, knockouts of the Grik1 gene have increased, while Grik2 and Grik4 knockouts have reduced anxiety-like behavior. To determine whether the NETO proteins regulate anxiety and fear through modulation of KARs, we undertook a comprehensive behavioral analysis of adult Neto1 and Neto2 mice. We observed no differences in anxiety-like behavior. However, in cued fear conditioning, Neto2 , but not Neto1 mice, showed higher fear expression and delayed extinction compared to wild type mice. We established, by in situ hybridization, that Neto2 was expressed in both excitatory and inhibitory neurons throughout the fear circuit including the medial prefrontal cortex, amygdala, and hippocampus. Finally, we demonstrated that the relative amount of synaptosomal KAR GLUK2/3 subunit was 20.8% lower in the ventral hippocampus and 36.5% lower in the medial prefrontal cortex in Neto2 compared to the Neto2 mice. The GLUK5 subunit abundance was reduced 23.8% in the ventral hippocampus and 16.9% in the amygdala. We conclude that Neto2 regulates fear expression and extinction in mice, and that its absence increases conditionability, a phenotype related to post-traumatic stress disorder and propose that this phenotype is mediated by reduced KAR subunit abundance at synapses of fear-associated brain regions.