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Neuronal Heterotopias Affect the Activities of Distant Brain Areas and Lead to Behavioral Deficits.
Ishii, Kazuhiro; Kubo, Ken-ichiro; Endo, Toshihiro; Yoshida, Keitaro; Benner, Seico; Ito, Yukiko; Aizawa, Hidenori; Aramaki, Michihiko; Yamanaka, Akihiro; Tanaka, Kohichi; Takata, Norio; Tanaka, Kenji F; Mimura, Masaru; Tohyama, Chiharu; Kakeyama, Masaki; Nakajima, Kazunori.
Afiliação
  • Ishii K; Department of Anatomy, Keio University School of Medicine, Tokyo, 160-8582, Japan.
  • Kubo K; Department of Anatomy, Keio University School of Medicine, Tokyo, 160-8582, Japan.
  • Endo T; Laboratory of Environmental Health Sciences, Center for Disease Biology and Integrative Medicine, Graduate School of Medicine, and Department of Neurochemistry, Graduate School of Medicine, University of Tokyo, Tokyo, 113-0033, Japan.
  • Yoshida K; Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, 160-8582, Japan.
  • Benner S; Laboratory of Environmental Health Sciences, Center for Disease Biology and Integrative Medicine, Graduate School of Medicine, and.
  • Ito Y; Laboratory of Molecular Neuroscience, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, 113-8510, Japan.
  • Aizawa H; Laboratory of Molecular Neuroscience, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, 113-8510, Japan, Department of Neurobiology, Institute of Biomedical and Health Sciences, Hiroshima University, Hiroshima, 734-8553, Japan.
  • Aramaki M; Department of Anatomy, Keio University School of Medicine, Tokyo, 160-8582, Japan.
  • Yamanaka A; Department of Neuroscience II, Research Institute of Environmental Medicine, Nagoya University, Nagoya, 464-8601, Japan.
  • Tanaka K; Laboratory of Molecular Neuroscience, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, 113-8510, Japan, Center for Brain Integration Research, Tokyo Medical and Dental University, Tokyo, 113-8510, Japan, and.
  • Takata N; Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, 160-8582, Japan.
  • Tanaka KF; Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, 160-8582, Japan.
  • Mimura M; Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, 160-8582, Japan.
  • Tohyama C; Laboratory of Environmental Health Sciences, Center for Disease Biology and Integrative Medicine, Graduate School of Medicine, and.
  • Kakeyama M; Laboratory of Environmental Health Sciences, Center for Disease Biology and Integrative Medicine, Graduate School of Medicine, and Laboratory for Systems Neuroscience and Preventive Medicine, Waseda University Faculty of Human Sciences, Saitama, 359-1192, Japan kazunori@keio.jp kake@waseda.jp.
  • Nakajima K; Department of Anatomy, Keio University School of Medicine, Tokyo, 160-8582, Japan, kazunori@keio.jp kake@waseda.jp.
J Neurosci ; 35(36): 12432-45, 2015 Sep 09.
Article em En | MEDLINE | ID: mdl-26354912
ABSTRACT
Neuronal heterotopia refers to brain malformations resulting from deficits of neuronal migration. Individuals with heterotopias show a high incidence of neurological deficits, such as epilepsy. More recently, it has come to be recognized that focal heterotopias may also show a range of psychiatric problems, including cognitive and behavioral impairments. However, because focal heterotopias are not always located in the brain areas responsible for the symptoms, the causal relationship between the symptoms and heterotopias remains elusive. In this study, we showed that mice with focal heterotopias in the somatosensory cortex generated by in utero electroporation exhibited spatial working memory deficit and low competitive dominance behavior, which have been shown to be closely associated with the activity of the medial prefrontal cortex (mPFC) in rodents. Analysis of the mPFC activity revealed that the immediate-early gene expression was decreased and the local field potentials of the mPFC were altered in the mice with heterotopias compared with the control mice. Moreover, activation of these ectopic and overlying sister neurons using the DREADD (designer receptor exclusively activated by designer drug) system improved the working memory deficits. These findings suggest that cortical regions containing focal heterotopias can affect distant brain regions and give rise to behavioral abnormalities. Significance statement Recent studies reported that patients with heterotopias have a variety of clinical symptoms, such as cognitive disturbance, psychiatric symptoms, and autistic behavior. However, the causal relationship between the symptoms and heterotopias remains elusive. Here we showed that mice with focal heterotopias in the somatosensory cortex generated by in utero electroporation exhibited behavioral deficits that have been shown to be associated with the mPFC activity in rodents. The existence of heterotopias indeed altered the neural activities of the mPFC, and direct manipulation of the neural activity of the ectopic neurons and their sister neurons in the overlying cortex improved the behavioral deficit. Thus, our results indicate that focal heterotopias could affect the activities of distant brain areas and cause behavioral abnormalities.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Córtex Somatossensorial / Córtex Pré-Frontal / Malformações do Desenvolvimento Cortical / Transtornos Mentais Tipo de estudo: Diagnostic_studies Limite: Animals Idioma: En Revista: J Neurosci Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Córtex Somatossensorial / Córtex Pré-Frontal / Malformações do Desenvolvimento Cortical / Transtornos Mentais Tipo de estudo: Diagnostic_studies Limite: Animals Idioma: En Revista: J Neurosci Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Japão