Cognitive dysfunction and prefrontal synaptic abnormalities in a mouse model of fragile X syndrome

D. D. Krueger, E. K. Osterweil, S. P. Chen, L. D. Tye, M. F. Bear

Research output: Contribution to journalArticlepeer-review


Among the hallmark phenotypes reported in individuals with fragile X syndrome (FXS) are deficits in attentional function, inhibitory control, and cognitive flexibility, a set of cognitive skills thought to be associated with the prefrontal cortex (PFC). However, despite substantial clinical research into these core deficits, the PFC has received surprisingly little attention in preclinical research, particularly in animal models of FXS. In this study, we sought to investigate the molecular, cellular, and behavioral consequences of the loss of the fragile X mental retardation protein in the PFC of Fmr1 KO mice, a mouse model of FXS. We identify a robust cognitive impairment in these mice that may be related to the deficits in cognitive flexibility observed in individuals with FXS. In addition, we report that levels of proteins involved in synaptic function, including the NMDA receptor subunits NR1, NR2A, and NR2B; the scaffolding proteins PSD-95 and SAPAP3; and the plasticity-related gene Arc, are decreased in the prefrontal cortex of Fmr1 KO mice and are partly correlated with behavioral performance. Finally, we report that expression of c-Fos, a marker of neuronal activity, is decreased in the PFC of Fmr1 KO mice. Together, these data suggest that Fmr1 KO mice may represent a valuable animal model for the PFC-associated molecular, cellular, and behavioral abnormalities in FXS and that this model may be useful for testing the efficacy of therapeutic strategies aimed at treating the cognitive impairments in FXS.
Original languageEnglish
Pages (from-to)2587-2592
JournalProceedings of the National Academy of Sciences (PNAS)
Issue number6
Publication statusPublished - 8 Feb 2011


Dive into the research topics of 'Cognitive dysfunction and prefrontal synaptic abnormalities in a mouse model of fragile X syndrome'. Together they form a unique fingerprint.

Cite this