Granule cells affect dendritic tree selection in purkinje cells during cerebellar development

Author:

Kato MizukiORCID,Schutter Erik DeORCID

Abstract

AbstractThis study investigates the interrelationship between primary dendrite selection of Purkinje cells and migration of their pre-synaptic partner granule cells during cerebellar development. During development of the cerebellar cortex, each Purkinje cell grows more than three dendritic trees, from which a primary tree is selected to develop further, whereas the others completely retract. Experimental studies suggest that this selection process is coordinated by physical and synaptic interactions with granule cells. However, technical limitations hinder a continuous experimental observation of multiple populations. To reveal the mechanism underlying this selection process, we constructed a computational model of dendritic developments and granule cell migrations, using a new computational framework, NeuroDevSim. Comparisons of the resulting morphologies from the model demonstrate the roles of the selection stage in regulating the growth of the selected primary trees. The study presents the first computational model that simultaneously simulates growing Purkinje cells and the dynamics of granule cell migrations, revealing the role of physical and synaptic interactions upon dendritic selection. The model provides new insights about the distinct planar morphology of Purkinje cell dendrites and about roles of the dendritic selection process during the cerebellar development. The model also supports the hypothesis that synaptic interactions by granule cells are likely to be involved in the selection procedure.Author SummaryThe mature structure of a Purkinje cell, the main neuron of the cerebellum, is composed of a large flat dendritic tree composed of a single or sometimes 2 primary dendrites. However, this neuron has multiple similar trees during development, and retracts most of them to select its primary tree. We aim to explore roles of this developmental process as either an important step to attain optimal morphology or merely a redundant step to be eliminated by evolution in the future. We especially focused on environmental interactions on Purkinje cells as criteria to select the dendritic tree, hypothesizing that developing an efficient network with other neurons is one of the main goals of neuronal morphology. We constructed and used computational models to investigate detailed physical interactions and communications between Purkinje cells and their environment. Comparisons of models suggest the role of the selection stage is to obtain favorable growth of primary trees.

Publisher

Cold Spring Harbor Laboratory

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3