학술논문

Direct and Collateral Alterations of Functional Cortical Circuits in a Rat Model of Subcortical Band Heterotopia.
Document Type
Academic Journal
Author
Plantier V; INMED, Aix-Marseille Université, INSERM UMR1249, Marseille 13009, France.; Watrin F; INMED, Aix-Marseille Université, INSERM UMR1249, Marseille 13009, France.; Buhler E; INMED, Aix-Marseille Université, INSERM UMR1249, Marseille 13009, France.; Martineau FS; INMED, Aix-Marseille Université, INSERM UMR1249, Marseille 13009, France.; Sahu S; INMED, Aix-Marseille Université, INSERM UMR1249, Marseille 13009, France.; Manent JB; INMED, Aix-Marseille Université, INSERM UMR1249, Marseille 13009, France.; Bureau I; INMED, Aix-Marseille Université, INSERM UMR1249, Marseille 13009, France.; Represa A; INMED, Aix-Marseille Université, INSERM UMR1249, Marseille 13009, France.
Source
Publisher: Oxford University Press Country of Publication: United States NLM ID: 9110718 Publication Model: Print Cited Medium: Internet ISSN: 1460-2199 (Electronic) Linking ISSN: 10473211 NLM ISO Abbreviation: Cereb Cortex Subsets: MEDLINE
Subject
Language
English
Abstract
Subcortical band heterotopia (SBH), also known as double-cortex syndrome, is a neuronal migration disorder characterized by an accumulation of neurons in a heterotopic band below the normotopic cortex. The majority of patients with SBH have mild to moderate intellectual disability and intractable epilepsy. However, it is still not clear how cortical networks are organized in SBH patients and how this abnormal organization contributes to improper brain function. In this study, cortical networks were investigated in the barrel cortex in an animal model of SBH induced by in utero knockdown of Dcx, main causative gene of this condition in human patients. When the SBH was localized below the Barrel Field (BF), layer (L) four projection to correctly positioned L2/3 pyramidal cells was weakened due to lower connectivity. Conversely, when the SBH was below an adjacent cortical region, the excitatory L4 to L2/3 projection was stronger due to increased L4 neuron excitability, synaptic strength and excitation/inhibition ratio of L4 to L2/3 connection. We propose that these developmental alterations contribute to the spectrum of clinical dysfunctions reported in patients with SBH.
(© The Author(s) 2018. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.)