The Lack of Emx2 Causes Impairment of Reelin Signaling and Defects of Neuronal Migration in the Developing Cerebral Cortex

Neocorticogenesis in mice homozygous for an Emx2 null allele is the topic of this article. The development of both main components of neocortex, primordial plexiform layer derivatives and cortical plate, was analyzed, paying special attention to radial migration of neurons forming the cortical plate...

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Veröffentlicht in:The Journal of neuroscience 2000-02, Vol.20 (3), p.1109-1118
Hauptverfasser: Mallamaci, Antonello, Mercurio, Sara, Muzio, Luca, Cecchi, Chiara, Pardini, Celia Leonor, Gruss, Peter, Boncinelli, Edoardo
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container_issue 3
container_start_page 1109
container_title The Journal of neuroscience
container_volume 20
creator Mallamaci, Antonello
Mercurio, Sara
Muzio, Luca
Cecchi, Chiara
Pardini, Celia Leonor
Gruss, Peter
Boncinelli, Edoardo
description Neocorticogenesis in mice homozygous for an Emx2 null allele is the topic of this article. The development of both main components of neocortex, primordial plexiform layer derivatives and cortical plate, was analyzed, paying special attention to radial migration of neurons forming the cortical plate. The products of the Reelin gene, normally playing a key role in orchestrating radial migration of these neurons, display normal distribution at the beginning of the cortical neuronogenesis but are absent in the neocortical marginal zone of the mutant mice at the time when the cortical plate is laid down. As a consequence, the development of radial glia is impaired, and neurons making up the cortical plate display abnormal migration patterns. In addition, restricted defects along the rostrocaudal and the mediolateral axes are present in the subplate, suggesting an Emx2-specific role in priming the proper development of this layer.
doi_str_mv 10.1523/JNEUROSCI.20-03-01109.2000
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source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
subjects Animals
Cell Adhesion Molecules, Neuronal - physiology
Cell Movement - physiology
Cerebral Cortex - embryology
Embryo, Mammalian - cytology
Embryonic and Fetal Development - physiology
Emx2 protein
Extracellular Matrix Proteins - physiology
Female
Homeodomain Proteins - genetics
Homeodomain Proteins - physiology
Mice
Mice, Inbred Strains
Mice, Knockout - genetics
Mutation - physiology
Nerve Tissue Proteins
Neuroglia - physiology
Neurons - physiology
reelin
Reelin Protein
Serine Endopeptidases
Signal Transduction - physiology
Transcription Factors
title The Lack of Emx2 Causes Impairment of Reelin Signaling and Defects of Neuronal Migration in the Developing Cerebral Cortex
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