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Brain Res. 2003 May 2;971(1):83-9.

Somatosensory cortical barrel dendritic abnormalities in a mouse model of the fragile X mental retardation syndrome.

Author information

1
Neuroscience Program, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA. rgalvez@uiuc.edu

Abstract

The Fragile X mental retardation syndrome is the largest source of inherited mental retardation. The syndrome usually results from the transcriptional silencing of the fragile X mental retardation gene (FMR1). To date the most prominent reported neuronal abnormalities for the fragile X mental retardation syndrome include a higher density of long thin spines similar to those found in sensory deprived and developing tissue, suggesting a possible deficit in pruning of immature spines. Dendrites on spiny stellate cells in the inner 1/3 of the barrel wall in layer IV of the rodent somatosensory cortex have been shown to exhibit developmental pruning similar to that affecting spines. To determine if FMRP plays a role in dendritic development, these neurons were examined in two strains of adult FMRP knockout (FraX) mice. FraX mice in both strains exhibited a greater amount of septa-oriented dendritic material, a morphology consistent with pre-pruning status early in development. This observation suggests that FMRP could be necessary for normal developmentally regulated dendritic pruning.

PMID:
12691840
DOI:
10.1016/s0006-8993(03)02363-1
[Indexed for MEDLINE]

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