Literature DB >> 10487203

The right neuron at the wrong place: biology of heterotopic neurons in cortical neuronal migration disorders, with special reference to associated pathologies.

N Chevassus-au-Louis1, A Represa.   

Abstract

During the development of the neocortex, neurogenesis and neuronal differentiation occur in two separate locations. Thus neurons have to migrate through the future white matter. Arrested or excessive migration leads neurons to differentiate in a heterotopic position. Such neuronal migration disorders (NMDs) occur sporadically in normal development but are markedly increased as a consequence of genetic defects or after exposure to toxic drugs during the period of migration. Anatomofunctional studies in rodents with NMDs have revealed that heterotopic neurons form essentially normal afferent and efferent connections, which has been interpreted as evidence that the connection pattern of cortical neurons is specified prior to migration. In addition, recent data show that heterotopic neurons can be contacted by environmental, that is local, fibres that normally never innervate the neocortex. This dual connectivity leads heterotopias to form bridges between their environmental and original network. Such an abnormal pattern of connectivity could contribute to the pathophysiology of disorders associated with NMDs such as epilepsy.

Entities:  

Mesh:

Year:  1999        PMID: 10487203     DOI: 10.1007/s000180050367

Source DB:  PubMed          Journal:  Cell Mol Life Sci        ISSN: 1420-682X            Impact factor:   9.261


  12 in total

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Authors:  Suzanne G Mueller; Kenneth D Laxer; Nathan Cashdollar; Shannon Buckley; Crystal Paul; Michael W Weiner
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3.  Individual differences in verbal abilities associated with regional blurring of the left gray and white matter boundary.

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4.  Metabolic characteristics of cortical malformations causing epilepsy.

Authors:  S G Mueller; K D Laxer; J A Barakos; N Cashdollar; D L Flenniken; P Vermathen; G B Matson; M W Weiner
Journal:  J Neurol       Date:  2005-04-29       Impact factor: 4.849

5.  Quantitative 1H-MRS reveals metabolic difference between subcategories of malformations of cortical development.

Authors:  Qiaoyue Tan; Wenyu Liu; Xinyue Wan; Weina Wang; Xiaorui Su; Huaiqiang Sun; Simin Zhang; Qiang Yue
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Review 6.  Cell migration in the normal and pathological postnatal mammalian brain.

Authors:  Myriam Cayre; Peter Canoll; James E Goldman
Journal:  Prog Neurobiol       Date:  2009-02-11       Impact factor: 11.685

7.  Organelle and cellular abnormalities associated with hippocampal heterotopia in neonatal doublecortin knockout mice.

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Journal:  PLoS One       Date:  2013-09-02       Impact factor: 3.240

8.  Advanced [(18)F]FDG and [(11)C]flumazenil PET analysis for individual outcome prediction after temporal lobe epilepsy surgery for hippocampal sclerosis.

Authors:  J Yankam Njiwa; K R Gray; N Costes; F Mauguiere; P Ryvlin; A Hammers
Journal:  Neuroimage Clin       Date:  2014-11-27       Impact factor: 4.881

9.  Epilepsy in Dcx knockout mice associated with discrete lamination defects and enhanced excitability in the hippocampus.

Authors:  Marika Nosten-Bertrand; Caroline Kappeler; Céline Dinocourt; Cécile Denis; Johanne Germain; Françoise Phan Dinh Tuy; Soraya Verstraeten; Chantal Alvarez; Christine Métin; Jamel Chelly; Bruno Giros; Richard Miles; Antoine Depaulis; Fiona Francis
Journal:  PLoS One       Date:  2008-06-25       Impact factor: 3.240

10.  Brain morphological defects in prolidase deficient mice: first report.

Authors:  V Insolia; V M Piccolini
Journal:  Eur J Histochem       Date:  2014-09-17       Impact factor: 3.188

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