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Differential roles of Netrin-1 and its receptor DCC in inferior olivary neuron migration
- Source :
- Molecular and Cellular Neuroscience, Molecular and Cellular Neuroscience, Elsevier, 2009, 41 (4), pp.429-39. ⟨10.1016/j.mcn.2009.04.008⟩, Molecular and Cellular Neuroscience, Elsevier, 2009, 41 (4), pp.429-39. 〈10.1016/j.mcn.2009.04.008〉
- Publication Year :
- 2009
- Publisher :
- HAL CCSD, 2009.
-
Abstract
- International audience; Netrin-1 was previously shown to be required for the tangential migration and survival of neurons that will form the inferior olivary nucleus (ION). Surprisingly, the compared analysis of mutant mice lacking either Netrin-1 or its major receptor DCC reveals striking phenotypic differences besides common features. Although ectopic stops of ION cell bodies occur in the same positions along the migratory stream in both mutants, the ION neurons' number is not affected by the lack of DCC whereas it is reduced in Netrin-1 mutant mice. Thus, cell death results from the absence of Netrin-1 and not from neuron mis-routing, arguing for a role of Netrin-1 as a survival factor in vivo. The secretion of Netrin-1 by the floor plate (FP) is strictly required - whereas DCC is not - to avoid ION axons' repulsion by the FP and allows them to cross it. Leading processes of neurons of other caudal precerebellar nuclei (PCN) cannot cross the FP in either mutant mouse, suggesting differential sensitivity or mechanism of action of Netrin-1 for leading processes of ION and other PCN neurons.
- Subjects :
- MESH: Olivary Nucleus
Mutant
MESH: Neurons
Mice
0302 clinical medicine
Cell Movement
Neural Pathways
Netrin
MESH: Gene Expression Regulation, Developmental
Inferior olivary nucleus
MESH: Animals
MESH: Nerve Tissue Proteins
Receptor
MESH: Cell Movement
MESH: Receptors, Cell Surface
Neurons
0303 health sciences
Gene Expression Regulation, Developmental
Netrin-1
DCC Receptor
Cell biology
medicine.anatomical_structure
embryonic structures
[SDV.NEU]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]
medicine.symptom
Programmed cell death
MESH: Axons
animal structures
MESH: Mutation
MESH: Mice, Transgenic
Neurogenesis
Mice, Transgenic
Nerve Tissue Proteins
Receptors, Cell Surface
Olivary Nucleus
Biology
03 medical and health sciences
Cellular and Molecular Neuroscience
Organ Culture Techniques
medicine
Animals
MESH: Tumor Suppressor Proteins
[SDV.NEU] Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]
Nerve Growth Factors
Molecular Biology
MESH: Mice
030304 developmental biology
Floor plate
MESH: Nerve Growth Factors
Tumor Suppressor Proteins
MESH: Neural Pathways
fungi
MESH: Embryo, Mammalian
Cell Biology
Embryo, Mammalian
Axons
MESH: Organ Culture Techniques
MESH: Neurogenesis
Mechanism of action
nervous system
Mutation
Neuron
Neuroscience
030217 neurology & neurosurgery
Subjects
Details
- Language :
- English
- ISSN :
- 10447431 and 10959327
- Database :
- OpenAIRE
- Journal :
- Molecular and Cellular Neuroscience, Molecular and Cellular Neuroscience, Elsevier, 2009, 41 (4), pp.429-39. ⟨10.1016/j.mcn.2009.04.008⟩, Molecular and Cellular Neuroscience, Elsevier, 2009, 41 (4), pp.429-39. 〈10.1016/j.mcn.2009.04.008〉
- Accession number :
- edsair.doi.dedup.....6457f47a4272be4a7ca279a140ac4c2a
- Full Text :
- https://doi.org/10.1016/j.mcn.2009.04.008⟩