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Retrograde BDNF to TrkB signaling promotes synapse elimination in the developing cerebellum
Elimination of early-formed redundant synapses during postnatal development is essential for functional neural circuit formation. Purkinje cells (PCs) in the neonatal cerebellum are innervated by multiple climbing fibers (CFs). A single CF is strengthened whereas the other CFs are eliminated in each...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5543168/ https://www.ncbi.nlm.nih.gov/pubmed/28775326 http://dx.doi.org/10.1038/s41467-017-00260-w |
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author | Choo, Myeongjeong Miyazaki, Taisuke Yamazaki, Maya Kawamura, Meiko Nakazawa, Takanobu Zhang, Jianling Tanimura, Asami Uesaka, Naofumi Watanabe, Masahiko Sakimura, Kenji Kano, Masanobu |
author_facet | Choo, Myeongjeong Miyazaki, Taisuke Yamazaki, Maya Kawamura, Meiko Nakazawa, Takanobu Zhang, Jianling Tanimura, Asami Uesaka, Naofumi Watanabe, Masahiko Sakimura, Kenji Kano, Masanobu |
author_sort | Choo, Myeongjeong |
collection | PubMed |
description | Elimination of early-formed redundant synapses during postnatal development is essential for functional neural circuit formation. Purkinje cells (PCs) in the neonatal cerebellum are innervated by multiple climbing fibers (CFs). A single CF is strengthened whereas the other CFs are eliminated in each PC dependent on postsynaptic activity in PC, but the underlying mechanisms are largely unknown. Here, we report that brain-derived neurotrophic factor (BDNF) from PC facilitates CF synapse elimination. By PC-specific deletion of BDNF combined with knockdown of BDNF receptors in CF, we show that BDNF acts retrogradely on TrkB in CFs, and facilitates elimination of CF synapses from PC somata during the third postnatal week. We also show that BDNF shares signaling pathway with metabotropic glutamate receptor 1, a key molecule that triggers a canonical pathway for CF synapse elimination. These results indicate that unlike other synapses, BDNF mediates punishment signal for synapse elimination in the developing cerebellum. |
format | Online Article Text |
id | pubmed-5543168 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55431682017-08-09 Retrograde BDNF to TrkB signaling promotes synapse elimination in the developing cerebellum Choo, Myeongjeong Miyazaki, Taisuke Yamazaki, Maya Kawamura, Meiko Nakazawa, Takanobu Zhang, Jianling Tanimura, Asami Uesaka, Naofumi Watanabe, Masahiko Sakimura, Kenji Kano, Masanobu Nat Commun Article Elimination of early-formed redundant synapses during postnatal development is essential for functional neural circuit formation. Purkinje cells (PCs) in the neonatal cerebellum are innervated by multiple climbing fibers (CFs). A single CF is strengthened whereas the other CFs are eliminated in each PC dependent on postsynaptic activity in PC, but the underlying mechanisms are largely unknown. Here, we report that brain-derived neurotrophic factor (BDNF) from PC facilitates CF synapse elimination. By PC-specific deletion of BDNF combined with knockdown of BDNF receptors in CF, we show that BDNF acts retrogradely on TrkB in CFs, and facilitates elimination of CF synapses from PC somata during the third postnatal week. We also show that BDNF shares signaling pathway with metabotropic glutamate receptor 1, a key molecule that triggers a canonical pathway for CF synapse elimination. These results indicate that unlike other synapses, BDNF mediates punishment signal for synapse elimination in the developing cerebellum. Nature Publishing Group UK 2017-08-04 /pmc/articles/PMC5543168/ /pubmed/28775326 http://dx.doi.org/10.1038/s41467-017-00260-w Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Choo, Myeongjeong Miyazaki, Taisuke Yamazaki, Maya Kawamura, Meiko Nakazawa, Takanobu Zhang, Jianling Tanimura, Asami Uesaka, Naofumi Watanabe, Masahiko Sakimura, Kenji Kano, Masanobu Retrograde BDNF to TrkB signaling promotes synapse elimination in the developing cerebellum |
title | Retrograde BDNF to TrkB signaling promotes synapse elimination in the developing cerebellum |
title_full | Retrograde BDNF to TrkB signaling promotes synapse elimination in the developing cerebellum |
title_fullStr | Retrograde BDNF to TrkB signaling promotes synapse elimination in the developing cerebellum |
title_full_unstemmed | Retrograde BDNF to TrkB signaling promotes synapse elimination in the developing cerebellum |
title_short | Retrograde BDNF to TrkB signaling promotes synapse elimination in the developing cerebellum |
title_sort | retrograde bdnf to trkb signaling promotes synapse elimination in the developing cerebellum |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5543168/ https://www.ncbi.nlm.nih.gov/pubmed/28775326 http://dx.doi.org/10.1038/s41467-017-00260-w |
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