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Developmental pattern and structural factors of dendritic survival in cerebellar granule cells in vivo
Granule cells (GCs) in the cerebellar cortex are important for sparse encoding of afferent sensorimotor information. Modeling studies show that GCs can perform their function most effectively when they have four dendrites. Indeed, mature GCs have four short dendrites on average, each terminating in...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6277421/ https://www.ncbi.nlm.nih.gov/pubmed/30510282 http://dx.doi.org/10.1038/s41598-018-35829-y |
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author | Dhar, Matasha Hantman, Adam W. Nishiyama, Hiroshi |
author_facet | Dhar, Matasha Hantman, Adam W. Nishiyama, Hiroshi |
author_sort | Dhar, Matasha |
collection | PubMed |
description | Granule cells (GCs) in the cerebellar cortex are important for sparse encoding of afferent sensorimotor information. Modeling studies show that GCs can perform their function most effectively when they have four dendrites. Indeed, mature GCs have four short dendrites on average, each terminating in a claw-like ending that receives both excitatory and inhibitory inputs. Immature GCs, however, have significantly more dendrites—all without claws. How these redundant dendrites are refined during development is largely unclear. Here, we used in vivo time-lapse imaging and immunohistochemistry to study developmental refinement of GC dendritic arbors and its relation to synapse formation. We found that while the formation of dendritic claws stabilized the dendrites, the selection of surviving dendrites was made before claw formation, and longer immature dendrites had a significantly higher chance of survival than shorter dendrites. Using immunohistochemistry, we show that glutamatergic and GABAergic synapses are transiently formed on immature GC dendrites, and the number of GABAergic, but not glutamatergic, synapses correlates with the length of immature dendrites. Together, these results suggest a potential role of transient GABAergic synapses on dendritic selection and show that preselected dendrites are stabilized by the formation of dendritic claws—the site of mature synapses. |
format | Online Article Text |
id | pubmed-6277421 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62774212018-12-06 Developmental pattern and structural factors of dendritic survival in cerebellar granule cells in vivo Dhar, Matasha Hantman, Adam W. Nishiyama, Hiroshi Sci Rep Article Granule cells (GCs) in the cerebellar cortex are important for sparse encoding of afferent sensorimotor information. Modeling studies show that GCs can perform their function most effectively when they have four dendrites. Indeed, mature GCs have four short dendrites on average, each terminating in a claw-like ending that receives both excitatory and inhibitory inputs. Immature GCs, however, have significantly more dendrites—all without claws. How these redundant dendrites are refined during development is largely unclear. Here, we used in vivo time-lapse imaging and immunohistochemistry to study developmental refinement of GC dendritic arbors and its relation to synapse formation. We found that while the formation of dendritic claws stabilized the dendrites, the selection of surviving dendrites was made before claw formation, and longer immature dendrites had a significantly higher chance of survival than shorter dendrites. Using immunohistochemistry, we show that glutamatergic and GABAergic synapses are transiently formed on immature GC dendrites, and the number of GABAergic, but not glutamatergic, synapses correlates with the length of immature dendrites. Together, these results suggest a potential role of transient GABAergic synapses on dendritic selection and show that preselected dendrites are stabilized by the formation of dendritic claws—the site of mature synapses. Nature Publishing Group UK 2018-12-03 /pmc/articles/PMC6277421/ /pubmed/30510282 http://dx.doi.org/10.1038/s41598-018-35829-y Text en © The Author(s) 2018 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 Dhar, Matasha Hantman, Adam W. Nishiyama, Hiroshi Developmental pattern and structural factors of dendritic survival in cerebellar granule cells in vivo |
title | Developmental pattern and structural factors of dendritic survival in cerebellar granule cells in vivo |
title_full | Developmental pattern and structural factors of dendritic survival in cerebellar granule cells in vivo |
title_fullStr | Developmental pattern and structural factors of dendritic survival in cerebellar granule cells in vivo |
title_full_unstemmed | Developmental pattern and structural factors of dendritic survival in cerebellar granule cells in vivo |
title_short | Developmental pattern and structural factors of dendritic survival in cerebellar granule cells in vivo |
title_sort | developmental pattern and structural factors of dendritic survival in cerebellar granule cells in vivo |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6277421/ https://www.ncbi.nlm.nih.gov/pubmed/30510282 http://dx.doi.org/10.1038/s41598-018-35829-y |
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