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基于基因敲除的炎症性肠病复合动物模型研究进展

[Research progress on composite animal models of inflammatory bowel disease based on gene knockout].

作者信息

Zhao Huihui, Tang Huifang

机构信息

Zhejiang University School of Medicine, Hangzhou 310058, China.

出版信息

Zhejiang Da Xue Xue Bao Yi Xue Ban. 2018 Dec 25;47(6):665-670. doi: 10.3785/j.issn.1008-9292.2018.12.16.

Abstract

Establishing a suitable animal model is important for studying the mechanism of inflammatory bowel disease (IBD) and exploring new therapeutic approaches. Although a large number of IBD single gene knockout animal models have been established, single knockout of certain genes associated with human IBD susceptibility does not manifest symptoms of IBD or manifest extremely milder symptoms, while composite animal models based on other modeling factors can better simulate the clinical features of IBD. This article mainly introduces three novel composite animal models and elaborates the possible pathogenesis of each composite model:animal models established by gene double knockout have more obvious and earlier symptoms than single-knockout models; single gene knockout model with Helicobacter infection can help to study the role of microbial infections in the pathogenesis of IBD; on the basis of gene knockout, specific deletion of certain immune cells can be used to study the role of the immune cells in the development of IBD. Among the above composite animal models, double knockout mice may be important animal models for IBD study.

摘要

建立合适的动物模型对于研究炎症性肠病(IBD)的发病机制和探索新的治疗方法至关重要。尽管已经建立了大量的IBD单基因敲除动物模型,但某些与人类IBD易感性相关的基因单敲除并不表现出IBD症状或仅表现出极其轻微的症状,而基于其他建模因素的复合动物模型可以更好地模拟IBD的临床特征。本文主要介绍了三种新型复合动物模型,并阐述了每种复合模型可能的发病机制:基因双敲除建立的动物模型比单敲除模型具有更明显和更早出现的症状;幽门螺杆菌感染的单基因敲除模型有助于研究微生物感染在IBD发病机制中的作用;在基因敲除的基础上,特异性删除某些免疫细胞可用于研究免疫细胞在IBD发展中的作用。在上述复合动物模型中,双敲除小鼠可能是IBD研究的重要动物模型。

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