Abstract
The signaling cascades governing neuronal migration are believed to link extracellular signals to cytoskeletal components. MAP1B is a neuron-specific microtubule-associated protein implicated in the control of the dynamic stability of microtubules and in the cross-talk between microtubules and actin filaments. Here we show that Reelin can induce mode I MAP1B phosphorylation, both in vivo and in vitro, through gsk3 and cdk5 activation. Additionally, mDab1 participates in the signaling cascade responsible for mode I MAP1B phosphorylation. Conversely, MAP1B-deficient mice display an abnormal structuring of the nervous system, especially in brain laminated areas, indicating a failure in neuronal migration. Therefore, we propose that Reelin can induce post-translational modifications on MAP1B that could correlate with its function in neuronal migration.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Cell Adhesion Molecules, Neuronal / biosynthesis
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Cell Adhesion Molecules, Neuronal / genetics
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Cell Adhesion Molecules, Neuronal / physiology*
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Cell Movement / physiology*
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Cells, Cultured
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Cerebral Cortex / cytology
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Cerebral Cortex / metabolism
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Extracellular Matrix Proteins / biosynthesis
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Extracellular Matrix Proteins / genetics
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Extracellular Matrix Proteins / physiology*
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Female
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Mice
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Mice, Transgenic
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Microtubule-Associated Proteins / deficiency
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Microtubule-Associated Proteins / genetics
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Microtubule-Associated Proteins / physiology*
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Nerve Tissue Proteins / biosynthesis
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Nerve Tissue Proteins / genetics
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Nerve Tissue Proteins / physiology*
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Neurons / cytology*
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Neurons / metabolism*
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Pregnancy
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Reelin Protein
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Serine Endopeptidases / biosynthesis
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Serine Endopeptidases / genetics
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Serine Endopeptidases / physiology*
Substances
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Cell Adhesion Molecules, Neuronal
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Extracellular Matrix Proteins
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Microtubule-Associated Proteins
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Nerve Tissue Proteins
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Reelin Protein
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microtubule-associated protein 1B
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Reln protein, mouse
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Serine Endopeptidases