Department of Molecular Biology and Immunology, University of North Texas Health Science Center at Fort Worth, Fort Worth, TX 76107, USA.
Int J Biol Sci. 2012;8(8):1156-67. doi: 10.7150/ijbs.5033. Epub 2012 Sep 24.
Mutation in the "nude" gene, i.e. the FoxN1 gene, induces a hairless phenotype and a rudimentary thymus gland in mice (nude mouse) and humans (T-cell related primary immunodeficiency). Conventional FoxN1 gene knockout and transgenic mouse models have been generated for studies of FoxN1 gene function related to skin and immune diseases, and for cancer models. It appeared that FoxN1's role was fully understood and the nude mouse model was fully utilized. However, in recent years, with the development of inducible gene knockout/knockin mouse models with the loxP-Cre(ER(T)) and diphtheria toxin receptor-induced cell abolished systems, it appears that the complete repertoire of FoxN1's roles and deep-going usage of nude mouse model in immune function studies have just begun. Here we summarize the research progress made by several recent works studying the role of FoxN1 in the thymus and utilizing nude and "second (conditional) nude" mouse models for studies of T-cell development and function. We also raise questions and propose further consideration of FoxN1 functions and utilizing this mouse model for immune function studies.
“裸体”基因(即 FoxN1 基因)的突变会导致小鼠(裸鼠)和人类(T 细胞相关原发性免疫缺陷)出现无毛表型和发育不全的胸腺。已经生成了常规的 FoxN1 基因敲除和转基因小鼠模型,用于研究 FoxN1 基因与皮肤和免疫疾病以及癌症模型相关的功能。似乎 FoxN1 的作用已经被充分理解,并且裸鼠模型已经被充分利用。然而,近年来,随着具有 loxP-Cre(ER(T))和白喉毒素受体诱导细胞消除系统的诱导型基因敲除/敲入小鼠模型的发展,似乎 FoxN1 的作用的完整范围以及在免疫功能研究中对裸鼠模型的深入应用才刚刚开始。在这里,我们总结了最近几项研究 FoxN1 在胸腺中的作用的研究进展,并利用裸鼠和“第二(条件性)裸鼠”模型研究 T 细胞的发育和功能。我们还提出了问题,并进一步考虑了 FoxN1 功能以及利用该小鼠模型进行免疫功能研究的问题。