Literature DB >> 21540240

Disrupted-in-Schizophrenia-1 (Disc1) is necessary for migration of the pyramidal neurons during mouse hippocampal development.

Kenji Tomita1, Ken-ichiro Kubo, Kazuhiro Ishii, Kazunori Nakajima.   

Abstract

The hippocampus has a highly ordered structure and is composed of distinct layers. Neuronal migration is an essential part of the process of the layer formation because neurons are primarily generated near the ventricle and must migrate to arrive at their final locations during brain development. Impairment of brain development is thought to underlie the etiology of psychiatric disorders. Consistent with this idea, many genetic risk factors for psychiatric disorders play critical roles during brain development. As one example, Disrupted-in-Schizophrenia-1 (DISC1) is a genetic risk factor for major psychiatric disorders and plays various roles during neurodevelopment. To examine the role of Disc1 in the hippocampal development, we suppressed expression of Disc1 in the CA1 region of the developing mouse hippocampus by using the RNA interference (RNAi) technology and an in utero electroporation system. Disc1 suppression was found to impair migration of the CA1 pyramidal neurons. This effect was especially apparent while the majority of the transfected neurons were passing through the stratum pyramidale of the developing hippocampus. The migration of neurons was restored by expression of an RNAi-resistant wild-type mouse Disc1, indicating that the migration defect was caused by specific suppression of Disc1. In the mature hippocampus, the migration defect resulted in malposition and disarray of the pyramidal neurons. These findings indicate that Disc1 is required for migration and layer formation by the CA1 pyramidal neurons during hippocampal development.

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Year:  2011        PMID: 21540240     DOI: 10.1093/hmg/ddr194

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  34 in total

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Journal:  Neurobiol Dis       Date:  2016-09-12       Impact factor: 5.996

Review 2.  DISC1 at 10: connecting psychiatric genetics and neuroscience.

Authors:  David J Porteous; J Kirsty Millar; Nicholas J Brandon; Akira Sawa
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3.  Rescue of CAMDI deletion-induced delayed radial migration and psychiatric behaviors by HDAC6 inhibitor.

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4.  Impaired Cerebellar Development in Mice Overexpressing VGF.

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Journal:  Neurochem Res       Date:  2018-11-20       Impact factor: 3.996

5.  Hippocampal shape abnormalities of patients with childhood-onset schizophrenia and their unaffected siblings.

Authors:  Sarah L M Johnson; Lei Wang; Kathryn I Alpert; Deanna Greenstein; Liv Clasen; Francois Lalonde; Rachel Miller; Judith Rapoport; Nitin Gogtay
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6.  Cortex-, Hippocampus-, Thalamus-, Hypothalamus-, Lateral Septal Nucleus- and Striatum-specific In Utero Electroporation in the C57BL/6 Mouse.

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7.  Chronic ketamine produces altered distribution of parvalbumin-positive cells in the hippocampus of adult rats.

Authors:  Jonathan J Sabbagh; Andrew S Murtishaw; Monica M Bolton; Chelcie F Heaney; Michael Langhardt; Jefferson W Kinney
Journal:  Neurosci Lett       Date:  2013-07-01       Impact factor: 3.046

8.  Suppression of DNA Double-Strand Break Formation by DNA Polymerase β in Active DNA Demethylation Is Required for Development of Hippocampal Pyramidal Neurons.

Authors:  Akiko Uyeda; Kohei Onishi; Teruyoshi Hirayama; Satoko Hattori; Tsuyoshi Miyakawa; Takeshi Yagi; Nobuhiko Yamamoto; Noriyuki Sugo
Journal:  J Neurosci       Date:  2020-10-21       Impact factor: 6.167

9.  Effects of genetic and environmental risk for schizophrenia on hippocampal activity and psychosis-like behavior in mice.

Authors:  Daniel Scott; Carol A Tamminga
Journal:  Behav Brain Res       Date:  2017-11-15       Impact factor: 3.332

10.  Protection of Radial Glial-Like Cells in the Hippocampus of APP/PS1 Mice: a Novel Mechanism of Memantine in the Treatment of Alzheimer's Disease.

Authors:  Dayu Sun; Junhua Chen; Xiaohang Bao; Yulong Cai; Jinghui Zhao; Jing Huang; Wei Huang; Xiaotang Fan; Haiwei Xu
Journal:  Mol Neurobiol       Date:  2014-09-09       Impact factor: 5.590

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