A Model for the Coexistence of Competing Mechanisms for Ca 2 + Oscillations in T-lymphocytes.

IF 2.2 4区 数学 Q2 BIOLOGY Bulletin of Mathematical Biology Pub Date : 2024-06-13 DOI:10.1007/s11538-024-01317-w
Paco Castaneda Ruan, J Cory Benson, Mohamed Trebak, Vivien Kirk, James Sneyd
{"title":"<ArticleTitle xmlns:ns0=\"http://www.w3.org/1998/Math/MathML\">A Model for the Coexistence of Competing Mechanisms for <ns0:math><ns0:msup><ns0:mtext>Ca</ns0:mtext> <ns0:mrow><ns0:mtext>2</ns0:mtext> <ns0:mo>+</ns0:mo></ns0:mrow> </ns0:msup> </ns0:math> Oscillations in T-lymphocytes.","authors":"Paco Castaneda Ruan, J Cory Benson, Mohamed Trebak, Vivien Kirk, James Sneyd","doi":"10.1007/s11538-024-01317-w","DOIUrl":null,"url":null,"abstract":"<p><p><math><msup><mtext>Ca</mtext> <mrow><mtext>2</mtext> <mo>+</mo></mrow> </msup> </math> is a ubiquitous signaling mechanism across different cell types. In T-cells, it is associated with cytokine production and immune function. Benson et al. have shown the coexistence of competing <math><msup><mtext>Ca</mtext> <mrow><mtext>2</mtext> <mo>+</mo></mrow> </msup> </math> oscillations during antigen stimulation of T-cell receptors, depending on the presence of extracellular <math><msup><mtext>Ca</mtext> <mrow><mtext>2</mtext> <mo>+</mo></mrow> </msup> </math> influx through the <math><msup><mtext>Ca</mtext> <mrow><mtext>2</mtext> <mo>+</mo></mrow> </msup> </math> release-activated <math><msup><mtext>Ca</mtext> <mrow><mtext>2</mtext> <mo>+</mo></mrow> </msup> </math> channel (Benson in J Biol Chem 29:105310, 2023). In this paper, we construct a mathematical model consisting of five ordinary differential equations and analyze the relationship between the competing oscillatory mechanisms.. We perform bifurcation analysis on two versions of our model, corresponding to the two oscillatory types, to find the defining characteristics of these two families.</p>","PeriodicalId":9372,"journal":{"name":"Bulletin of Mathematical Biology","volume":"86 7","pages":"86"},"PeriodicalIF":2.2000,"publicationDate":"2024-06-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11176111/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bulletin of Mathematical Biology","FirstCategoryId":"100","ListUrlMain":"https://doi.org/10.1007/s11538-024-01317-w","RegionNum":4,"RegionCategory":"数学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Ca 2 + is a ubiquitous signaling mechanism across different cell types. In T-cells, it is associated with cytokine production and immune function. Benson et al. have shown the coexistence of competing Ca 2 + oscillations during antigen stimulation of T-cell receptors, depending on the presence of extracellular Ca 2 + influx through the Ca 2 + release-activated Ca 2 + channel (Benson in J Biol Chem 29:105310, 2023). In this paper, we construct a mathematical model consisting of five ordinary differential equations and analyze the relationship between the competing oscillatory mechanisms.. We perform bifurcation analysis on two versions of our model, corresponding to the two oscillatory types, to find the defining characteristics of these two families.

Abstract Image

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
T 淋巴细胞中 Ca 2 + 振荡的竞争机制共存模型
Ca 2 + 是不同类型细胞中普遍存在的信号机制。在 T 细胞中,它与细胞因子的产生和免疫功能有关。Benson 等人的研究表明,在抗原刺激 T 细胞受体的过程中,根据通过 Ca 2 + 释放激活的 Ca 2 + 通道流入细胞外 Ca 2 + 的情况,会同时出现相互竞争的 Ca 2 + 振荡(Benson,J Biol Chem 29:105310, 2023)。在本文中,我们构建了一个由五个常微分方程组成的数学模型,并分析了相互竞争的振荡机制之间的关系。我们对与两种振荡类型相对应的两个版本的模型进行了分岔分析,以找到这两个家族的决定性特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
3.90
自引率
8.60%
发文量
123
审稿时长
7.5 months
期刊介绍: The Bulletin of Mathematical Biology, the official journal of the Society for Mathematical Biology, disseminates original research findings and other information relevant to the interface of biology and the mathematical sciences. Contributions should have relevance to both fields. In order to accommodate the broad scope of new developments, the journal accepts a variety of contributions, including: Original research articles focused on new biological insights gained with the help of tools from the mathematical sciences or new mathematical tools and methods with demonstrated applicability to biological investigations Research in mathematical biology education Reviews Commentaries Perspectives, and contributions that discuss issues important to the profession All contributions are peer-reviewed.
期刊最新文献
Environmental Stochasticity Drives Adaptation to Cooler Thermal Optima in Competition. Characterising Epigenetic Tipping Points using a Spectral Dimension Reduction Approach. Effect of Preventive Measures and Heterogeneity of Sexual Contacts on Zika virus Transmission. Effects of Multi-Phase Control Mechanism on Fibroblast Dynamics: A Segmented Mathematical Modeling Approach. Counting Spinal Phylogenetic Networks.
×
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:604180095
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