Hexagons all the way down: grid cells as a conformal isometric map of space.

IF 3.8 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS PLoS Computational Biology Pub Date : 2025-02-13 DOI:10.1371/journal.pcbi.1012804
Vemund Sigmundson Schøyen, Kosio Beshkov, Markus Borud Pettersen, Erik Hermansen, Konstantin Holzhausen, Anders Malthe-Sørenssen, Marianne Fyhn, Mikkel Elle Lepperød
{"title":"Hexagons all the way down: grid cells as a conformal isometric map of space.","authors":"Vemund Sigmundson Schøyen, Kosio Beshkov, Markus Borud Pettersen, Erik Hermansen, Konstantin Holzhausen, Anders Malthe-Sørenssen, Marianne Fyhn, Mikkel Elle Lepperød","doi":"10.1371/journal.pcbi.1012804","DOIUrl":null,"url":null,"abstract":"<p><p>Grid cells in the entorhinal cortex are known for their hexagonal spatial activity patterns and are thought to provide a neural metric for space, and support path integration. In this study, we further investigate grid cells as a metric of space by optimising them for a conformal isometric (CI) map of space using a model based on a superposition of plane waves. By optimising the phases within a single grid cell module, we find that the module can form a CI of two-dimensional flat space with phases arranging into a regular hexagonal pattern, supporting an accurate spatial metric. Additionally, we find that experimentally recorded grid cells exhibit CI properties, with one example module showing a phase arrangement similar to the hexagonal pattern observed in our model. These findings provide computational and preliminary experimental support for grid cells as a CI-based spatial representation. We also examine other properties that emerge in CI-optimised modules, including consistent energy expenditure across space and the minimal cell count required to support unique representation of space and maximally topologically persistent toroidal population activity. Altogether, our results suggest that grid cells are well-suited to form a CI map, with several beneficial properties arising from this organisation.</p>","PeriodicalId":20241,"journal":{"name":"PLoS Computational Biology","volume":"21 2","pages":"e1012804"},"PeriodicalIF":3.8000,"publicationDate":"2025-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"PLoS Computational Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1371/journal.pcbi.1012804","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0

Abstract

Grid cells in the entorhinal cortex are known for their hexagonal spatial activity patterns and are thought to provide a neural metric for space, and support path integration. In this study, we further investigate grid cells as a metric of space by optimising them for a conformal isometric (CI) map of space using a model based on a superposition of plane waves. By optimising the phases within a single grid cell module, we find that the module can form a CI of two-dimensional flat space with phases arranging into a regular hexagonal pattern, supporting an accurate spatial metric. Additionally, we find that experimentally recorded grid cells exhibit CI properties, with one example module showing a phase arrangement similar to the hexagonal pattern observed in our model. These findings provide computational and preliminary experimental support for grid cells as a CI-based spatial representation. We also examine other properties that emerge in CI-optimised modules, including consistent energy expenditure across space and the minimal cell count required to support unique representation of space and maximally topologically persistent toroidal population activity. Altogether, our results suggest that grid cells are well-suited to form a CI map, with several beneficial properties arising from this organisation.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
求助全文
约1分钟内获得全文 去求助
来源期刊
PLoS Computational Biology
PLoS Computational Biology BIOCHEMICAL RESEARCH METHODS-MATHEMATICAL & COMPUTATIONAL BIOLOGY
CiteScore
7.10
自引率
4.70%
发文量
820
审稿时长
2.5 months
期刊介绍: PLOS Computational Biology features works of exceptional significance that further our understanding of living systems at all scales—from molecules and cells, to patient populations and ecosystems—through the application of computational methods. Readers include life and computational scientists, who can take the important findings presented here to the next level of discovery. Research articles must be declared as belonging to a relevant section. More information about the sections can be found in the submission guidelines. Research articles should model aspects of biological systems, demonstrate both methodological and scientific novelty, and provide profound new biological insights. Generally, reliability and significance of biological discovery through computation should be validated and enriched by experimental studies. Inclusion of experimental validation is not required for publication, but should be referenced where possible. Inclusion of experimental validation of a modest biological discovery through computation does not render a manuscript suitable for PLOS Computational Biology. Research articles specifically designated as Methods papers should describe outstanding methods of exceptional importance that have been shown, or have the promise to provide new biological insights. The method must already be widely adopted, or have the promise of wide adoption by a broad community of users. Enhancements to existing published methods will only be considered if those enhancements bring exceptional new capabilities.
期刊最新文献
An in silico framework for the rational design of vaginal probiotic therapy. Ten simple rules for fostering creativity in research labs. Using a multi-strain infectious disease model with physical information neural networks to study the time dependence of SARS-CoV-2 variants of concern. Integrating multiscale mathematical modeling and multidimensional data reveals the effects of epigenetic instability on acquired drug resistance in cancer. Bimodality in E. coli gene expression: Sources and robustness to genome-wide stresses.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1