• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

病毒介导的合胞体形成的数学建模:过去的成功与未来的方向。

Mathematical Modeling of Virus-Mediated Syncytia Formation: Past Successes and Future Directions.

机构信息

Department of Physics & Astronomy, Texas Christian University, Fort Worth, TX, USA.

出版信息

Results Probl Cell Differ. 2024;71:345-370. doi: 10.1007/978-3-031-37936-9_17.

DOI:10.1007/978-3-031-37936-9_17
PMID:37996686
Abstract

Many viruses have the ability to cause cells to fuse into large multi-nucleated cells, known as syncytia. While the existence of syncytia has long been known and its importance in helping spread viral infection within a host has been understood, few mathematical models have incorporated syncytia formation or examined its role in viral dynamics. This review examines mathematical models that have incorporated virus-mediated cell fusion and the insights they have provided on how syncytia can change the time course of an infection. While the modeling efforts are limited, they show promise in helping us understand the consequences of syncytia formation if future modeling efforts can be coupled with appropriate experimental efforts to help validate the models.

摘要

许多病毒具有使细胞融合成大多核细胞的能力,称为合胞体。虽然合胞体的存在早已为人所知,其在帮助病毒在宿主内传播方面的重要性也已被理解,但很少有数学模型将合胞体的形成纳入其中,也很少有模型研究其在病毒动力学中的作用。这篇综述检查了纳入病毒介导的细胞融合的数学模型,以及它们提供的关于合胞体如何改变感染时间进程的见解。虽然建模工作有限,但如果未来的建模工作能够与适当的实验努力相结合,帮助验证模型,它们有望帮助我们理解合胞体形成的后果。

相似文献

1
Mathematical Modeling of Virus-Mediated Syncytia Formation: Past Successes and Future Directions.病毒介导的合胞体形成的数学建模:过去的成功与未来的方向。
Results Probl Cell Differ. 2024;71:345-370. doi: 10.1007/978-3-031-37936-9_17.
2
Multiscale moving boundary modelling of cancer interactions with a fusogenic oncolytic virus: The impact of syncytia dynamics.癌症与融合性溶瘤病毒相互作用的多尺度运动边界建模:合胞体动力学的影响。
Math Biosci. 2020 May;323:108296. doi: 10.1016/j.mbs.2019.108296. Epub 2019 Dec 27.
3
Analysis of a mathematical model for tumor therapy with a fusogenic oncolytic virus.一种融合性溶瘤病毒肿瘤治疗数学模型的分析
Math Biosci. 2015 Dec;270(Pt B):169-82. doi: 10.1016/j.mbs.2015.02.009. Epub 2015 Mar 2.
4
Virus-Induced Cell Fusion and Syncytia Formation.病毒诱导的细胞融合与合胞体形成。
Results Probl Cell Differ. 2024;71:283-318. doi: 10.1007/978-3-031-37936-9_14.
5
The role of syncytia during viral infections.合胞体在病毒感染中的作用。
J Theor Biol. 2021 Sep 21;525:110749. doi: 10.1016/j.jtbi.2021.110749. Epub 2021 May 5.
6
Syncytia Formation in Oncolytic Virotherapy.溶瘤病毒疗法中的多核巨细胞形成
Mol Ther Oncolytics. 2019 Oct 1;15:131-139. doi: 10.1016/j.omto.2019.09.006. eCollection 2019 Dec 20.
7
Virus-mediated cell fusion of SARS-CoV-2 variants.病毒介导的 SARS-CoV-2 变体细胞融合。
Math Biosci. 2024 Mar;369:109144. doi: 10.1016/j.mbs.2024.109144. Epub 2024 Jan 13.
8
Outer nuclear membrane fusion of adjacent nuclei in varicella-zoster virus-induced syncytia.水痘带状疱疹病毒诱导的多核巨细胞中相邻细胞核的外核膜融合。
Virology. 2017 Dec;512:34-38. doi: 10.1016/j.virol.2017.09.002. Epub 2017 Sep 11.
9
Syncytia formation by SARS-CoV-2-infected cells.SARS-CoV-2 感染细胞的合胞体形成。
EMBO J. 2020 Dec 1;39(23):e106267. doi: 10.15252/embj.2020106267. Epub 2020 Nov 4.
10
Impact of Induced Syncytia Formation on the Oncolytic Potential of Myxoma Virus.诱导合胞体形成对黏液瘤病毒溶瘤潜力的影响。
Oncolytic Virother. 2019 Dec 9;8:57-69. doi: 10.2147/OV.S220420. eCollection 2019.

本文引用的文献

1
Pan-coronavirus fusion inhibitors to combat COVID-19 and other emerging coronavirus infectious diseases.泛冠状病毒融合抑制剂用于应对 COVID-19 和其他新发冠状病毒传染病。
J Med Virol. 2023 Jan;95(1):e28143. doi: 10.1002/jmv.28143. Epub 2022 Sep 22.
2
Antiviral strategies against human metapneumovirus: Targeting the fusion protein.针对人类偏肺病毒的抗病毒策略:针对融合蛋白。
Antiviral Res. 2022 Nov;207:105405. doi: 10.1016/j.antiviral.2022.105405. Epub 2022 Sep 6.
3
ADAM10 and ADAM17 promote SARS-CoV-2 cell entry and spike protein-mediated lung cell fusion.
ADAM10 和 ADAM17 促进了 SARS-CoV-2 进入细胞以及刺突蛋白介导的肺细胞融合。
EMBO Rep. 2022 Jun 7;23(6):e54305. doi: 10.15252/embr.202154305. Epub 2022 May 8.
4
SARS-CoV-2 spike protein-induced cell fusion activates the cGAS-STING pathway and the interferon response.严重急性呼吸综合征冠状病毒2(SARS-CoV-2)刺突蛋白诱导的细胞融合激活了环鸟苷酸-腺苷酸合成酶-干扰素基因刺激蛋白(cGAS-STING)途径和干扰素反应。
Sci Signal. 2022 Apr 12;15(729):eabg8744. doi: 10.1126/scisignal.abg8744.
5
Human Organotypic Airway and Lung Organoid Cells of Bronchiolar and Alveolar Differentiation Are Permissive to Infection by Influenza and SARS-CoV-2 Respiratory Virus.人器官型气道和肺泡分化的肺类器官细胞允许流感和 SARS-CoV-2 呼吸道病毒感染。
Front Cell Infect Microbiol. 2022 Mar 14;12:841447. doi: 10.3389/fcimb.2022.841447. eCollection 2022.
6
Distinctive Roles of Furin and TMPRSS2 in SARS-CoV-2 Infectivity.弗林蛋白酶和 TMPRSS2 在 SARS-CoV-2 感染中的独特作用。
J Virol. 2022 Apr 27;96(8):e0012822. doi: 10.1128/jvi.00128-22. Epub 2022 Mar 28.
7
Computational Prediction of Bacteriophage Host Ranges.噬菌体宿主范围的计算预测
Microorganisms. 2022 Jan 12;10(1):149. doi: 10.3390/microorganisms10010149.
8
Short-Stalk Isoforms of CADM1 and CADM2 Trigger Neuropathogenic Measles Virus-Mediated Membrane Fusion by Interacting with the Viral Hemagglutinin.CADM1 和 CADM2 的短柄同种型通过与病毒血凝素相互作用触发致病性麻疹病毒介导的膜融合。
J Virol. 2022 Feb 9;96(3):e0194921. doi: 10.1128/JVI.01949-21. Epub 2021 Nov 17.
9
Cell-Cell Fusion Mediated by Viruses and HERV-Derived Fusogens in Cancer Initiation and Progression.病毒和人内源性逆转录病毒衍生融合蛋白介导的细胞-细胞融合在癌症起始和进展中的作用
Cancers (Basel). 2021 Oct 26;13(21):5363. doi: 10.3390/cancers13215363.
10
Tetraspanins: Host Factors in Viral Infections.四跨膜蛋白:病毒感染中的宿主因素。
Int J Mol Sci. 2021 Oct 27;22(21):11609. doi: 10.3390/ijms222111609.