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Dysregulation of synaptic plasticity precedes appearance of morphological defects in a Pten conditional knockout mouse model of autism.

The phosphoinositide signaling system is a crucial regulator of neural development, cell survival, and plasticity. Phosphatase and tensin homolog deleted on chromosome 10 (PTEN) negatively regulates phosphatidylinositol 3-kinase signaling and downstream targets. Nse-Cre Pten conditional knockout mice, in which Pten is ablated in granule cells of the dentate gyrus and pyramidal neurons of the hippocampal CA3, but not CA1, recapitulate many of the symptoms of humans with inactivating PTEN mutations, including progressive hypertrophy of the dentate gyrus and deficits in hippocampus-based social and cognitive behaviors. However, the impact of Pten loss on activity-dependent synaptic plasticity in this clinically relevant mouse model of Pten inactivation remains unclear. Here, we show that two phosphatidylinositol 3-kinase- and protein synthesis-dependent forms of synaptic plasticity, theta burst-induced long-term potentiation and metabotropic glutamate receptor (mGluR)-dependent long-term depression, are dysregulated at medial perforant path-to-dentate gyrus synapses of young Nse-Cre Pten conditional knockout mice before the onset of visible morphological abnormalities. In contrast, long-term potentiation and mGluR-dependent long-term depression are normal at CA3-CA1 pyramidal cell synapses at this age. Our results reveal that deletion of Pten in dentate granule cells dysregulates synaptic plasticity, a defect that may underlie abnormal social and cognitive behaviors observed in humans with Pten inactivating mutations and potentially other autism spectrum disorders.

Pubmed ID: 23487788

Authors

  • Takeuchi K
  • Gertner MJ
  • Zhou J
  • Parada LF
  • Bennett MV
  • Zukin RS

Journal

Proceedings of the National Academy of Sciences of the United States of America

Publication Data

March 19, 2013

Associated Grants

  • Agency: NINDS NIH HHS, Id: 1P50NS052606
  • Agency: NIMH NIH HHS, Id: MH092877
  • Agency: NIMH NIH HHS, Id: R01 MH092877
  • Agency: NINDS NIH HHS, Id: R01 NS046742

Mesh Terms

  • Aging
  • Animals
  • Autistic Disorder
  • Disease Models, Animal
  • Hippocampus
  • Humans
  • Long-Term Potentiation
  • Mice
  • Mice, Knockout
  • Mutation
  • Nerve Tissue Proteins
  • PTEN Phosphohydrolase
  • Phosphatidylinositol 3-Kinases
  • Receptors, Metabotropic Glutamate
  • Signal Transduction
  • Synapses