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Development of Axon-Target Specificity of Ponto-Cerebellar Afferents
The function of neuronal networks relies on selective assembly of synaptic connections during development. We examined how synaptic specificity emerges in the pontocerebellar projection. Analysis of axon-target interactions with correlated light-electron microscopy revealed that developing pontine m...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3035609/ https://www.ncbi.nlm.nih.gov/pubmed/21346800 http://dx.doi.org/10.1371/journal.pbio.1001013 |
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author | Kalinovsky, Anna Boukhtouche, Fatiha Blazeski, Richard Bornmann, Caroline Suzuki, Noboru Mason, Carol A. Scheiffele, Peter |
author_facet | Kalinovsky, Anna Boukhtouche, Fatiha Blazeski, Richard Bornmann, Caroline Suzuki, Noboru Mason, Carol A. Scheiffele, Peter |
author_sort | Kalinovsky, Anna |
collection | PubMed |
description | The function of neuronal networks relies on selective assembly of synaptic connections during development. We examined how synaptic specificity emerges in the pontocerebellar projection. Analysis of axon-target interactions with correlated light-electron microscopy revealed that developing pontine mossy fibers elaborate extensive cell-cell contacts and synaptic connections with Purkinje cells, an inappropriate target. Subsequently, mossy fiber–Purkinje cell connections are eliminated resulting in granule cell-specific mossy fiber connectivity as observed in mature cerebellar circuits. Formation of mossy fiber-Purkinje cell contacts is negatively regulated by Purkinje cell-derived BMP4. BMP4 limits mossy fiber growth in vitro and Purkinje cell-specific ablation of BMP4 in mice results in exuberant mossy fiber–Purkinje cell interactions. These findings demonstrate that synaptic specificity in the pontocerebellar projection is achieved through a stepwise mechanism that entails transient innervation of Purkinje cells, followed by synapse elimination. Moreover, this work establishes BMP4 as a retrograde signal that regulates the axon-target interactions during development. |
format | Text |
id | pubmed-3035609 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-30356092011-02-23 Development of Axon-Target Specificity of Ponto-Cerebellar Afferents Kalinovsky, Anna Boukhtouche, Fatiha Blazeski, Richard Bornmann, Caroline Suzuki, Noboru Mason, Carol A. Scheiffele, Peter PLoS Biol Research Article The function of neuronal networks relies on selective assembly of synaptic connections during development. We examined how synaptic specificity emerges in the pontocerebellar projection. Analysis of axon-target interactions with correlated light-electron microscopy revealed that developing pontine mossy fibers elaborate extensive cell-cell contacts and synaptic connections with Purkinje cells, an inappropriate target. Subsequently, mossy fiber–Purkinje cell connections are eliminated resulting in granule cell-specific mossy fiber connectivity as observed in mature cerebellar circuits. Formation of mossy fiber-Purkinje cell contacts is negatively regulated by Purkinje cell-derived BMP4. BMP4 limits mossy fiber growth in vitro and Purkinje cell-specific ablation of BMP4 in mice results in exuberant mossy fiber–Purkinje cell interactions. These findings demonstrate that synaptic specificity in the pontocerebellar projection is achieved through a stepwise mechanism that entails transient innervation of Purkinje cells, followed by synapse elimination. Moreover, this work establishes BMP4 as a retrograde signal that regulates the axon-target interactions during development. Public Library of Science 2011-02-08 /pmc/articles/PMC3035609/ /pubmed/21346800 http://dx.doi.org/10.1371/journal.pbio.1001013 Text en Kalinovsky et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Kalinovsky, Anna Boukhtouche, Fatiha Blazeski, Richard Bornmann, Caroline Suzuki, Noboru Mason, Carol A. Scheiffele, Peter Development of Axon-Target Specificity of Ponto-Cerebellar Afferents |
title | Development of Axon-Target Specificity of Ponto-Cerebellar Afferents |
title_full | Development of Axon-Target Specificity of Ponto-Cerebellar Afferents |
title_fullStr | Development of Axon-Target Specificity of Ponto-Cerebellar Afferents |
title_full_unstemmed | Development of Axon-Target Specificity of Ponto-Cerebellar Afferents |
title_short | Development of Axon-Target Specificity of Ponto-Cerebellar Afferents |
title_sort | development of axon-target specificity of ponto-cerebellar afferents |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3035609/ https://www.ncbi.nlm.nih.gov/pubmed/21346800 http://dx.doi.org/10.1371/journal.pbio.1001013 |
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