Frontal cortical synaptic communication is abnormal in Disc1 genetic mouse models of schizophrenia

Sandra M. Holley, Elizabeth A. Wang, Carlos Cepeda, J. David Jentsch, Christopher A Ross, Mikhail Pletnikov, Michael S. Levine

Research output: Contribution to journalArticle

Abstract

Mouse models carrying Disc1 mutations may provide insights into how Disc1 genetic variations contribute to schizophrenia (SZ) susceptibility. Disc1 mutant mice show behavioral and cognitive disturbances reminiscent of SZ. To dissect the synaptic mechanisms underlying these phenotypes, we examined electrophysiological properties of cortical neurons from two mouse models, the first expressing a truncated mouse Disc1 (mDisc1) protein throughout the entire brain, and the second expressing a truncated human Disc1 (hDisc1) protein in forebrain regions. We obtained whole-cell patch clamp recordings to examine how altered expression of Disc1 protein changes excitatory and inhibitory synaptic transmissions onto cortical pyramidal neurons in the medial prefrontal cortex in 4-7. month-old mDisc1 and hDisc1 mice. In both mDisc1 and hDisc1 mice, the frequency of spontaneous EPSCs was greater than in wild-type littermate controls. Male mice from both lines were more affected by the Disc1 mutation than were females, exhibiting increases in the ratio of excitatory to inhibitory events. Changes in spontaneous IPSCs were only observed in the mDisc1 model and were sex-specific, with diminished cortical GABAergic neurotransmission, a well-documented characteristic of SZ, occurring only in male mDisc1 mice. In contrast, female mDisc1 mice showed an increase in the frequency of small-amplitude sIPSCs. These findings indicate that truncations of Disc1 alter glutamatergic and GABAergic neurotransmission both commonly and differently in the models and some of the effects are sex-specific, revealing how altered Disc1 expression may contribute to behavioral disruptions and cognitive deficits of SZ.

Original languageEnglish (US)
Pages (from-to)264-272
Number of pages9
JournalSchizophrenia Research
Volume146
Issue number1-3
DOIs
StatePublished - May 2013

Fingerprint

Genetic Models
Schizophrenia
Communication
Synaptic Transmission
Mutation
Pyramidal Cells
Prosencephalon
Prefrontal Cortex
Proteins

Keywords

  • Disc1
  • Electrophysiology
  • EPSCs
  • Genetic mouse models
  • Glutamate
  • Patch clamp
  • Schizophrenia
  • Synaptic activity

ASJC Scopus subject areas

  • Psychiatry and Mental health
  • Biological Psychiatry

Cite this

Frontal cortical synaptic communication is abnormal in Disc1 genetic mouse models of schizophrenia. / Holley, Sandra M.; Wang, Elizabeth A.; Cepeda, Carlos; Jentsch, J. David; Ross, Christopher A; Pletnikov, Mikhail; Levine, Michael S.

In: Schizophrenia Research, Vol. 146, No. 1-3, 05.2013, p. 264-272.

Research output: Contribution to journalArticle

Holley, Sandra M. ; Wang, Elizabeth A. ; Cepeda, Carlos ; Jentsch, J. David ; Ross, Christopher A ; Pletnikov, Mikhail ; Levine, Michael S. / Frontal cortical synaptic communication is abnormal in Disc1 genetic mouse models of schizophrenia. In: Schizophrenia Research. 2013 ; Vol. 146, No. 1-3. pp. 264-272.
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