4.6 Article

Mice lacking neuronal calcium sensor-1 show social and cognitive deficits

期刊

BEHAVIOURAL BRAIN RESEARCH
卷 381, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.bbr.2019.112420

关键词

Neuronal calcium sensor-1; NCS-1; Frequenin; Autism spectrum disorder; Social approach; Behavioural flexibility; Long-Term potentiation; Long-Term depression; Spine density; Hippocampus; Dentate gyrus

资金

  1. Canadian Institutes of Health Research (CIHR) [147865, 111865, 111198]
  2. CIHR
  3. McLaughlin Centre
  4. Tier 1 Research Chair in Learning and Memory
  5. Ontario Mental Health Foundation (OMHF)
  6. CIHR Foundation [154276]
  7. Brain Canada Foundation through the Canada Brain Research Fund
  8. Health Canada

向作者/读者索取更多资源

Neuronal calcium sensor-1 or Frequenin is a calcium sensor widely expressed in the nervous system, with roles in neurotransmission, neurite outgrowth, synaptic plasticity, learning, and motivated behaviours. Neuronal calcium sensor-1 has been implicated in neuropsychiatric disorders including autism spectrum disorder, schizophrenia, and bipolar disorder. However, the role of neuronal calcium sensor-1 in behavioural phenotypes and brain changes relevant to autism spectrum disorder have not been evaluated. We show that neuronal calcium sensor-1 deletion in the mouse leads to a mild deficit in social approach and impaired displaced object recognition without affecting social interactions, behavioural flexibility, spatial reference memory, anxiety-like behaviour, or sensorimotor gating. Morphologically, neuronal calcium sensor-1 deletion leads to increased dendritic arbour complexity in the frontal cortex. At the level of hippocampal synaptic plasticity, neuronal calcium sensor-1 deletion leads to a reduction in long-term potentiation in the dentate gyrus, but not area Cornu Ammonis 1. Metabotropic glutamate receptor-induced long-term depression was unaffected in both dentate and Cornu Ammonis 1. These studies identify roles for neuronal calcium sensor-1 in specific subregions of the brain including a phenotype relevant to neuropsychiatric disorders.

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