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Semaphorin3A–neuropilin1 signalling is involved in the generation of cortical interneurons
Cortical interneurons are generated predominantly in the medial ganglionic eminence of the ventral telencephalon and migrate to the cortex during embryonic development. These cells express neuropilin (Nrp1 and Nrp2) receptors which mediate their response to the chemorepulsive class 3 semaphorin (Sem...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5504245/ https://www.ncbi.nlm.nih.gov/pubmed/27858201 http://dx.doi.org/10.1007/s00429-016-1337-3 |
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author | Andrews, William D. Barber, Melissa Nemitz, Marion Memi, Fani Parnavelas, John G. |
author_facet | Andrews, William D. Barber, Melissa Nemitz, Marion Memi, Fani Parnavelas, John G. |
author_sort | Andrews, William D. |
collection | PubMed |
description | Cortical interneurons are generated predominantly in the medial ganglionic eminence of the ventral telencephalon and migrate to the cortex during embryonic development. These cells express neuropilin (Nrp1 and Nrp2) receptors which mediate their response to the chemorepulsive class 3 semaphorin (Sema) ligands. We show here that semaphorins Sema3A and Sema3F are expressed in layers adjacent to cortical interneuron migratory streams as well as in the striatum, suggesting they may have a role in guiding these cells throughout their journey. Analysis of Sema3A (−/−) and Sema3F (−/−) mice during corticogenesis showed that absence of Sema3A, but not Sema3F, leads to aberrant migration of cortical interneurons through the striatum. Reduced number of cortical interneurons was found in the cortex of Sema3A (−/−), Nrp1 (−/−) and Nrp2 (−/−) mice, as well as altered distribution in Sema3F (−/−), Nrp1 (−/−), Nrp2 (−/−) animals and especially in neuropilin double mutants. The observed decrease in interneurons in Sema3A (−/−) and Nrp1 (−/−) mice was due to altered proliferative activity of their progenitors highlighted by changes in their mitotic spindle positioning and angle of cleavage plane during cell division. These findings point to a novel role for Sema3A–Nrp1 signalling in progenitor cell dynamics and in the generation of interneurons in the ventral telencephalon. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00429-016-1337-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5504245 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-55042452017-07-25 Semaphorin3A–neuropilin1 signalling is involved in the generation of cortical interneurons Andrews, William D. Barber, Melissa Nemitz, Marion Memi, Fani Parnavelas, John G. Brain Struct Funct Original Article Cortical interneurons are generated predominantly in the medial ganglionic eminence of the ventral telencephalon and migrate to the cortex during embryonic development. These cells express neuropilin (Nrp1 and Nrp2) receptors which mediate their response to the chemorepulsive class 3 semaphorin (Sema) ligands. We show here that semaphorins Sema3A and Sema3F are expressed in layers adjacent to cortical interneuron migratory streams as well as in the striatum, suggesting they may have a role in guiding these cells throughout their journey. Analysis of Sema3A (−/−) and Sema3F (−/−) mice during corticogenesis showed that absence of Sema3A, but not Sema3F, leads to aberrant migration of cortical interneurons through the striatum. Reduced number of cortical interneurons was found in the cortex of Sema3A (−/−), Nrp1 (−/−) and Nrp2 (−/−) mice, as well as altered distribution in Sema3F (−/−), Nrp1 (−/−), Nrp2 (−/−) animals and especially in neuropilin double mutants. The observed decrease in interneurons in Sema3A (−/−) and Nrp1 (−/−) mice was due to altered proliferative activity of their progenitors highlighted by changes in their mitotic spindle positioning and angle of cleavage plane during cell division. These findings point to a novel role for Sema3A–Nrp1 signalling in progenitor cell dynamics and in the generation of interneurons in the ventral telencephalon. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00429-016-1337-3) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2016-11-17 2017 /pmc/articles/PMC5504245/ /pubmed/27858201 http://dx.doi.org/10.1007/s00429-016-1337-3 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Andrews, William D. Barber, Melissa Nemitz, Marion Memi, Fani Parnavelas, John G. Semaphorin3A–neuropilin1 signalling is involved in the generation of cortical interneurons |
title | Semaphorin3A–neuropilin1 signalling is involved in the generation of cortical interneurons |
title_full | Semaphorin3A–neuropilin1 signalling is involved in the generation of cortical interneurons |
title_fullStr | Semaphorin3A–neuropilin1 signalling is involved in the generation of cortical interneurons |
title_full_unstemmed | Semaphorin3A–neuropilin1 signalling is involved in the generation of cortical interneurons |
title_short | Semaphorin3A–neuropilin1 signalling is involved in the generation of cortical interneurons |
title_sort | semaphorin3a–neuropilin1 signalling is involved in the generation of cortical interneurons |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5504245/ https://www.ncbi.nlm.nih.gov/pubmed/27858201 http://dx.doi.org/10.1007/s00429-016-1337-3 |
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