Deletion of Fmr1 from Forebrain Excitatory Neurons Triggers Abnormal Cellular, EEG, and Behavioral Phenotypes in the Auditory Cortex of a Mouse Model of Fragile X Syndrome. (29th July 2019)

• Record Type: Journal Article
• Authors: Lovelace, Jonathan W; Rais, Maham; Palacios, Arnold R; Shuai, Xinghao S; Bishay, Steven; Popa, Otilia; Pirbhoy, Patricia S; Binder, Devin K; Nelson, David L; Ethell, Iryna M; Razak, Khaleel A
• Is Part Of: Cerebral cortex. Volume 30:Number 3(2020)
• Page Start: 969
• Page End: 988
• Publication Date: 2019-07-29
• Subjects: autism -- cortical deficits -- fragile X syndrome -- perineuronal nets -- sensory processing disorders; Cerebral cortex -- Periodicals; Brain -- Periodicals; 612.825
• DOI: 10.1093/cercor/bhz141
• Languages: English
• ISSNs: 1047-3211

Abstract

Abstract: Fragile X syndrome (FXS) is a leading genetic cause of autism with symptoms that include sensory processing deficits. In both humans with FXS and a mouse model [ Fmr1 knockout (KO) mouse], electroencephalographic (EEG) recordings show enhanced resting state gamma power and reduced sound-evoked gamma synchrony. We previously showed that elevated levels of matrix metalloproteinase-9 (MMP-9) may contribute to these phenotypes by affecting perineuronal nets (PNNs) around parvalbumin (PV) interneurons in the auditory cortex of Fmr1 KO mice. However, how different cell types within local cortical circuits contribute to these deficits is not known. Here, we examined whether Fmr1 deletion in forebrain excitatory neurons affects neural oscillations, MMP-9 activity, and PV/PNN expression in the auditory cortex. We found that cortical MMP-9 gelatinase activity, mTOR/Akt phosphorylation, and resting EEG gamma power were enhanced in Cre Nex1 /Fmr1 Flox/y conditional KO (cKO) mice, whereas the density of PV/PNN cells was reduced. The Cre Nex1 /Fmr1 Flox/y cKO mice also show increased locomotor activity, but not the anxiety-like behaviors. These results indicate that fragile X mental retardation protein changes in excitatory neurons in the cortex are sufficient to elicit cellular, electrophysiological, and behavioral phenotypes in Fmr1 KO mice. More broadly, these results indicate that local cortical circuit abnormalities contribute to sensory processing deficits in autism spectrum disorders.