TitleConserved hippocampal cellular pathophysiology but distinct behavioural deficits in a new rat model of FXS.
Publication TypeJournal Article
Year of Publication2015
AuthorsTill SM, Asiminas A, Jackson AD, Katsanevaki D, Barnes SA, Osterweil EK, Bear MF, Chattarji S, Wood ER, Wyllie DJA, Kind PC
JournalHum Mol Genet
Volume24
Issue21
Pagination5977-84
Date Published2015 Nov 1
ISSN1460-2083
Abstract

Recent advances in techniques for manipulating genomes have allowed the generation of transgenic animals other than mice. These new models enable cross-mammalian comparison of neurological disease from core cellular pathophysiology to circuit and behavioural endophenotypes. Moreover they will enable us to directly test whether common cellular dysfunction or behavioural outcomes of a genetic mutation are more conserved across species. Using a new rat model of Fragile X Syndrome, we report that Fmr1 knockout (KO) rats exhibit elevated basal protein synthesis and an increase in mGluR-dependent long-term depression in CA1 of the hippocampus that is independent of new protein synthesis. These defects in plasticity are accompanied by an increase in dendritic spine density selectively in apical dendrites and subtle changes in dendritic spine morphology of CA1 pyramidal neurons. Behaviourally, Fmr1 KO rats show deficits in hippocampal-dependent, but not hippocampal-independent, forms of associative recognition memory indicating that the loss of fragile X mental retardation protein (FMRP) causes defects in episodic-like memory. In contrast to previous reports from mice, Fmr1 KO rats show no deficits in spatial reference memory reversal learning. One-trial spatial learning in a delayed matching to place water maze task was also not affected by the loss of FMRP in rats. This is the first evidence for conservation across mammalian species of cellular and physiological hippocampal phenotypes associated with the loss of FMRP. Furthermore, while key cellular phenotypes are conserved they manifest in distinct behavioural dysfunction. Finally, our data reveal novel information about the selective role of FMRP in hippocampus-dependent associative memory.

DOI10.1093/hmg/ddv299
Alternate JournalHum. Mol. Genet.
PubMed ID26243794
PubMed Central IDPMC4599667
Grant ListG0700967 / / Medical Research Council / United Kingdom
G0700967 / / Medical Research Council / United Kingdom
MR/K014137/1 / / Medical Research Council / United Kingdom
MR/K014137/1 / / Medical Research Council / United Kingdom