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耗尽树突状细胞的小鼠模型的优缺点。

Advantages and limitations of mouse models to deplete dendritic cells.

机构信息

Immunobiology Laboratory, London Research Institute, Cancer Research UK, London, United Kingdom.

出版信息

Eur J Immunol. 2013 Jan;43(1):22-6. doi: 10.1002/eji.201243022.

Abstract

Dendritic cells (DCs) play a key role in regulating innate and adaptive immunity. Our understanding of DC biology has benefited from studies in CD11c.DTR and CD11c.DOG mouse models that use the CD11c promoter to express a diphtheria toxin (DT) receptor transgene to inducibly deplete CD11c(+) cells. Other models to inducibly deplete specific DC subsets upon administration of DT have also been generated. However, most models suffer from limitations such as depletion of additional cell types or the requirement to be used as radiation chimeras. Moreover, CD11c.DTR and CD11c.DOG mice have recently been reported to display neutrophilia and monocytosis upon DT injection. We discuss here some of the limitations that should be taken into consideration when interpreting results obtained with mouse models of DC ablation.

摘要

树突状细胞 (DCs) 在调节先天和适应性免疫中发挥着关键作用。我们对 DC 生物学的理解得益于 CD11c.DTR 和 CD11c.DOG 小鼠模型的研究,这些模型利用 CD11c 启动子表达白喉毒素 (DT) 受体转基因,以诱导性耗尽 CD11c(+)细胞。还产生了其他模型,可在给予 DT 时诱导特定的 DC 亚群耗竭。然而,大多数模型存在局限性,例如耗尽其他细胞类型或需要作为辐射嵌合体使用。此外,最近有报道称,CD11c.DTR 和 CD11c.DOG 小鼠在注射 DT 后会出现中性粒细胞增多和单核细胞增多。我们在这里讨论了在解释 DC 消融小鼠模型的结果时应考虑的一些局限性。

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