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Principles of branch dynamics governing shape characteristics of cerebellar Purkinje cell dendrites
Neurons develop dendritic arbors in cell type-specific patterns. Using growing Purkinje cells in culture as a model, we performed a long-term time-lapse observation of dendrite branch dynamics to understand the rules that govern the characteristic space-filling dendrites. We found that dendrite arch...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Company of Biologists
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3491647/ https://www.ncbi.nlm.nih.gov/pubmed/22912417 http://dx.doi.org/10.1242/dev.081315 |
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author | Fujishima, Kazuto Horie, Ryota Mochizuki, Atsushi Kengaku, Mineko |
author_facet | Fujishima, Kazuto Horie, Ryota Mochizuki, Atsushi Kengaku, Mineko |
author_sort | Fujishima, Kazuto |
collection | PubMed |
description | Neurons develop dendritic arbors in cell type-specific patterns. Using growing Purkinje cells in culture as a model, we performed a long-term time-lapse observation of dendrite branch dynamics to understand the rules that govern the characteristic space-filling dendrites. We found that dendrite architecture was sculpted by a combination of reproducible dynamic processes, including constant tip elongation, stochastic terminal branching, and retraction triggered by contacts between growing dendrites. Inhibition of protein kinase C/protein kinase D signaling prevented branch retraction and significantly altered the characteristic morphology of long proximal segments. A computer simulation of dendrite branch dynamics using simple parameters from experimental measurements reproduced the time-dependent changes in the dendrite configuration in live Purkinje cells. Furthermore, perturbation analysis to parameters in silico validated the important contribution of dendritic retraction in the formation of the characteristic morphology. We present an approach using live imaging and computer simulations to clarify the fundamental mechanisms of dendrite patterning in the developing brain. |
format | Online Article Text |
id | pubmed-3491647 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Company of Biologists |
record_format | MEDLINE/PubMed |
spelling | pubmed-34916472012-11-15 Principles of branch dynamics governing shape characteristics of cerebellar Purkinje cell dendrites Fujishima, Kazuto Horie, Ryota Mochizuki, Atsushi Kengaku, Mineko Development Research Articles Neurons develop dendritic arbors in cell type-specific patterns. Using growing Purkinje cells in culture as a model, we performed a long-term time-lapse observation of dendrite branch dynamics to understand the rules that govern the characteristic space-filling dendrites. We found that dendrite architecture was sculpted by a combination of reproducible dynamic processes, including constant tip elongation, stochastic terminal branching, and retraction triggered by contacts between growing dendrites. Inhibition of protein kinase C/protein kinase D signaling prevented branch retraction and significantly altered the characteristic morphology of long proximal segments. A computer simulation of dendrite branch dynamics using simple parameters from experimental measurements reproduced the time-dependent changes in the dendrite configuration in live Purkinje cells. Furthermore, perturbation analysis to parameters in silico validated the important contribution of dendritic retraction in the formation of the characteristic morphology. We present an approach using live imaging and computer simulations to clarify the fundamental mechanisms of dendrite patterning in the developing brain. Company of Biologists 2012-09-15 /pmc/articles/PMC3491647/ /pubmed/22912417 http://dx.doi.org/10.1242/dev.081315 Text en © 2012. http://creativecommons.org/licenses/by-nc-sa/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial Share Alike License (http://creativecommons.org/licenses/by-nc-sa/3.0), which permits unrestricted non-commercial use, distribution and reproduction in any medium provided that the original work is properly cited and all further distributions of the work or adaptation are subject to the same Creative Commons License terms. |
spellingShingle | Research Articles Fujishima, Kazuto Horie, Ryota Mochizuki, Atsushi Kengaku, Mineko Principles of branch dynamics governing shape characteristics of cerebellar Purkinje cell dendrites |
title | Principles of branch dynamics governing shape characteristics of cerebellar Purkinje cell dendrites |
title_full | Principles of branch dynamics governing shape characteristics of cerebellar Purkinje cell dendrites |
title_fullStr | Principles of branch dynamics governing shape characteristics of cerebellar Purkinje cell dendrites |
title_full_unstemmed | Principles of branch dynamics governing shape characteristics of cerebellar Purkinje cell dendrites |
title_short | Principles of branch dynamics governing shape characteristics of cerebellar Purkinje cell dendrites |
title_sort | principles of branch dynamics governing shape characteristics of cerebellar purkinje cell dendrites |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3491647/ https://www.ncbi.nlm.nih.gov/pubmed/22912417 http://dx.doi.org/10.1242/dev.081315 |
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