Failed stabilization for long-term potentiation in the auditory cortex of Fmr1 knockout mice

Sungchil Yang, Sunggu Yang, Jae Sung Park, Alfredo Kirkwood, Shaowen Bao

Research output: Contribution to journalArticlepeer-review

13 Scopus citations

Abstract

Fragile X syndrome is a developmental disorder that affects sensory systems. A null mutation of the Fragile X Mental Retardation protein 1 (Fmr1) gene in mice has varied effects on developmental plasticity in different sensory systems, including normal barrel cortical plasticity, altered ocular dominance plasticity and grossly impaired auditory frequency map plasticity. The mutation also has different effects on long-term synaptic plasticity in somatosensory and visual cortical neurons, providing insights on how it may differentially affect the sensory systems. Here we present evidence that long-term potentiation (LTP) is impaired in the developing auditory cortex of the Fmr1 knockout (KO) mice. This impairment of synaptic plasticity is consistent with impaired frequency map plasticity in the Fmr1 KO mouse. Together, these results suggest a potential role of LTP in sensory map plasticity during early sensory development.

Original languageEnglish (US)
Article numbere104691
JournalPloS one
Volume9
Issue number8
DOIs
StatePublished - Aug 12 2014

ASJC Scopus subject areas

  • General Biochemistry, Genetics and Molecular Biology
  • General Agricultural and Biological Sciences
  • General

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