病毒介导的合胞体形成的数学建模:过去的成功和未来的方向。

Q4 Biochemistry, Genetics and Molecular Biology
Hana M Dobrovolny
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引用次数: 0

摘要

许多病毒有能力使细胞融合成大的多核细胞,称为合胞体。虽然合胞体的存在早已为人所知,其在帮助病毒感染在宿主内传播中的重要性也已被了解,但很少有数学模型将合胞体的形成纳入其中,或研究其在病毒动力学中的作用。这篇综述检查了包含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。虽然建模工作是有限的,但如果未来的建模工作可以与适当的实验工作相结合,以帮助验证模型,它们有望帮助我们理解合胞体形成的后果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mathematical Modeling of Virus-Mediated Syncytia Formation: Past Successes and Future Directions.

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.

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来源期刊
Results and Problems in Cell Differentiation
Results and Problems in Cell Differentiation Biochemistry, Genetics and Molecular Biology-Developmental Biology
CiteScore
1.90
自引率
0.00%
发文量
21
期刊介绍: Results and Problems in Cell Differentiation is an up-to-date book series that presents and explores selected questions of cell and developmental biology. Each volume focuses on a single, well-defined topic. Reviews address basic questions and phenomena, but also provide concise information on the most recent advances. Together, the volumes provide a valuable overview of this exciting and dynamically expanding field.
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