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组织工程学中的新方法:改进的病毒感染模型

New Methods in Tissue Engineering: Improved Models for Viral Infection.

作者信息

Ramanan Vyas, Scull Margaret A, Sheahan Timothy P, Rice Charles M, Bhatia Sangeeta N

机构信息

Harvard-MIT Division of Health Sciences and Technology, Institute for Medical Engineering and Science, Cambridge, Massachusetts 02139.

Center for the Study of Hepatitis C, Laboratory of Virology and Infectious Disease, The Rockefeller University, New York, NY 10065.

出版信息

Annu Rev Virol. 2014 Nov;1:475-499. doi: 10.1146/annurev-virology-031413-085437.

Abstract

New insights in the study of virus and host biology in the context of viral infection are made possible by the development of model systems that faithfully recapitulate the in vivo viral life cycle. Standard tissue culture models lack critical emergent properties driven by cellular organization and in vivo-like function, whereas animal models suffer from limited susceptibility to relevant human viruses and make it difficult to perform detailed molecular manipulation and analysis. Tissue engineering techniques may enable virologists to create infection models that combine the facile manipulation and readouts of tissue culture with the virus-relevant complexity of animal models. Here, we review the state of the art in tissue engineering and describe how tissue engineering techniques may alleviate some common shortcomings of existing models of viral infection, with a particular emphasis on hepatotropic viruses. We then discuss possible future applications of tissue engineering to virology, including current challenges and potential solutions.

摘要

在病毒感染背景下对病毒与宿主生物学的研究取得了新进展,这得益于能够忠实地重现体内病毒生命周期的模型系统的发展。标准的组织培养模型缺乏由细胞组织和类似体内功能驱动的关键涌现特性,而动物模型对相关人类病毒的易感性有限,并且难以进行详细的分子操作和分析。组织工程技术可能使病毒学家能够创建感染模型,将组织培养的简便操作和读数与动物模型中与病毒相关的复杂性结合起来。在这里,我们综述了组织工程的现状,并描述了组织工程技术如何减轻现有病毒感染模型的一些常见缺点,特别强调嗜肝病毒。然后,我们讨论了组织工程在病毒学中未来可能的应用,包括当前的挑战和潜在的解决方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/260a/4398347/c2cf44575fd9/nihms-666820-f0001.jpg

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Cell Stem Cell. 2014 Mar 6;14(3):267-9. doi: 10.1016/j.stem.2014.02.010.
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Pluripotent stem cell-derived hepatocyte-like cells.多能干细胞来源的肝细胞样细胞。
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