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Related Experiment Video

Updated: Jun 22, 2026

Ex Vivo Imaging of Postnatal Cerebellar Granule Cell Migration Using Confocal Macroscopy
09:10

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Published on: May 12, 2015

Disc1 regulates granule cell migration in the developing hippocampus.

Kate D Meyer1, Jill A Morris

  • 1Department of Pediatrics, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.

Human Molecular Genetics
|June 9, 2009
PubMed
Summary
This summary is machine-generated.

Investigating the Disrupted-In-Schizophrenia 1 (DISC1) gene

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Last Updated: Jun 22, 2026

Ex Vivo Imaging of Postnatal Cerebellar Granule Cell Migration Using Confocal Macroscopy
09:10

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Published on: May 12, 2015

Ex Vivo Culture of Chick Cerebellar Slices and Spatially Targeted Electroporation of Granule Cell Precursors
10:02

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Published on: December 14, 2015

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07:14

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Area of Science:

  • Neuroscience
  • Psychiatric Genetics
  • Developmental Biology

Background:

  • Schizophrenia is a debilitating psychiatric disorder linked to neurodevelopmental abnormalities.
  • The hippocampus shows structural and functional deficits in schizophrenia patients.
  • The role of the DISC1 gene in hippocampal development is not fully understood.

Purpose of the Study:

  • To investigate the function of the DISC1 gene in the development of the hippocampus.
  • To understand how DISC1 influences hippocampal neurodevelopment and its potential link to schizophrenia.

Main Methods:

  • In utero electroporation of Disc1 shRNA in developing mouse hippocampus.
  • Analysis of neuronal migration patterns, specifically dentate gyrus granule cells and CA1 pyramidal neurons.

Main Results:

  • Disc1 knockdown via shRNA hindered the migration of dentate gyrus granule cells.
  • Disc1 knockdown did not affect the migration of CA1 pyramidal neurons.
  • This suggests a spatially restricted role for DISC1 in hippocampal neuronal migration.

Conclusions:

  • DISC1 plays a crucial role in the proper migration of specific hippocampal neurons during development.
  • Abnormalities in DISC1 function may contribute to schizophrenia pathogenesis by disrupting hippocampal development.
  • These findings highlight DISC1 as a potential target for understanding and treating schizophrenia.