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PlexinD1 and Sema3E determine laminar positioning of heterotopically projecting callosal neurons
- Source :
- Molecular and Cellular Neuroscience, Molecular and Cellular Neuroscience, 1970, 100, pp.103397. ⟨10.1016/j.mcn.2019.103397⟩, Molecular and Cellular Neuroscience, Elsevier, 2019, 100, pp.103397. ⟨10.1016/j.mcn.2019.103397⟩, Digital.CSIC. Repositorio Institucional del CSIC, instname, Molecular and Cellular Neuroscience, Elsevier, 1970, 100, pp.103397. ⟨10.1016/j.mcn.2019.103397⟩, Digital.CSIC: Repositorio Institucional del CSIC, Consejo Superior de Investigaciones Científicas (CSIC), Molecular and Cellular Neuroscience, 2019, 100, pp.103397. ⟨10.1016/j.mcn.2019.103397⟩
- Publication Year :
- 1970
- Publisher :
- HAL CCSD, 1970.
-
Abstract
- © 2019 The Authors.<br />The corpus callosum is the largest bundle of commissural fibres that transfer information between the two cerebral hemispheres. Callosal projection neurons (CPNs) are a diverse population of pyramidal neurons within the neocortex that mainly interconnect homotopic regions of the opposite cortices. Nevertheless, some CPNs are involved in heterotopic projections between distinct cortical areas or to subcortical regions such as the striatum. In this study, we showed that the axon guidance receptor PlexinD1 is expressed by a large proportion of heterotopically projecting CPNs in layer 5A of the primary somatosensory (S1) and motor (M1) areas. Retrograde tracing of M1 CPNs projecting to the contralateral striatum revealed the presence of ectopic neurons aberrantly located in layers 2/3 of Plxnd1 and Sema3e mutant cortices. These results showed that Sema3E/PlexinD1 signalling controls the laminar distribution of heterotopically projecting CPNs.<br />This work was supported by the Centre National de la Recherche Scientifique (CNRS), France; Aix Marseille Université, France; Agence Nationale de la Recherche, ANR-12-BSV4-0012-01, France to F.M.; Fondation pour la Recherche Medicale, Equipe FRM DEQ20150331728, France to F.M., Institut Universitaire de France, France, to S.C.. T.V. is a recipient of doctoral fellowships from the Integrative and Clinical Neuroscience PhD Program and from the Fondation pour la Recherche Medicale, France.
- Subjects :
- 0301 basic medicine
Male
MESH: Neuroanatomical Tract-Tracing Techniques
[SDV]Life Sciences [q-bio]
[SDV.NEU.NB]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]/Neurobiology
MESH: Membrane Glycoproteins
MESH: Neurons
MESH: Semaphorins
Striatum
Semaphorins
Somatosensory system
Corpus callosum
Corpus Callosum
Mice
0302 clinical medicine
MESH: Animals
Neurons
Neocortex
Membrane Glycoproteins
Intracellular Signaling Peptides and Proteins
Motor Cortex
Commissure
3. Good health
Neuroanatomical Tract-Tracing Techniques
medicine.anatomical_structure
Female
Biology
MESH: Corpus Callosum
MESH: Motor Cortex
MESH: Somatosensory Cortex
03 medical and health sciences
Cellular and Molecular Neuroscience
MESH: Mice, Inbred C57BL
MESH: Intracellular Signaling Peptides and Proteins
medicine
Animals
Molecular Biology
MESH: Mice
Cell Biology
Somatosensory Cortex
Retrograde tracing
MESH: Male
Mice, Inbred C57BL
030104 developmental biology
Diverse population
nervous system
Axon guidance
Neuroscience
MESH: Female
030217 neurology & neurosurgery
Subjects
Details
- Language :
- English
- ISSN :
- 10447431 and 10959327
- Database :
- OpenAIRE
- Journal :
- Molecular and Cellular Neuroscience, Molecular and Cellular Neuroscience, 1970, 100, pp.103397. ⟨10.1016/j.mcn.2019.103397⟩, Molecular and Cellular Neuroscience, Elsevier, 2019, 100, pp.103397. ⟨10.1016/j.mcn.2019.103397⟩, Digital.CSIC. Repositorio Institucional del CSIC, instname, Molecular and Cellular Neuroscience, Elsevier, 1970, 100, pp.103397. ⟨10.1016/j.mcn.2019.103397⟩, Digital.CSIC: Repositorio Institucional del CSIC, Consejo Superior de Investigaciones Científicas (CSIC), Molecular and Cellular Neuroscience, 2019, 100, pp.103397. ⟨10.1016/j.mcn.2019.103397⟩
- Accession number :
- edsair.doi.dedup.....340f56b85f64f900cf70ceda4af1f284
- Full Text :
- https://doi.org/10.1016/j.mcn.2019.103397⟩