Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Kalinovsky, Anna, Boukhtouche, Fatiha, Blazeski, Richard, Bornmann, Caroline, Suzuki, Noboru, Mason, Carol A., Scheiffele, Peter
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
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
_version_ 1782197795259678720
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
work_keys_str_mv AT kalinovskyanna developmentofaxontargetspecificityofpontocerebellarafferents
AT boukhtouchefatiha developmentofaxontargetspecificityofpontocerebellarafferents
AT blazeskirichard developmentofaxontargetspecificityofpontocerebellarafferents
AT bornmanncaroline developmentofaxontargetspecificityofpontocerebellarafferents
AT suzukinoboru developmentofaxontargetspecificityofpontocerebellarafferents
AT masoncarola developmentofaxontargetspecificityofpontocerebellarafferents
AT scheiffelepeter developmentofaxontargetspecificityofpontocerebellarafferents