A Similar Mutation in the AAUU-Rich Elements of the Mouse TNF Gene Results in a Distinct Ileocolitic Phenotype: A New Strain of TNF-Overexpressing Mice.

IF 4.5 3区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Inflammatory Bowel Diseases Pub Date : 2025-01-04 DOI:10.1093/ibd/izae307
Amruth Chilukuri, Margaret Kim, Taniya Mitra, John M Gubatan, Josef Urrete, Leo D Saxon, Amber Ablack, Zbigniew Mikulski, Katarzyna Dobaczewska, Zining Shen, Mary Keir, Tangsheng Yi, Prabhdeep Kaur, Patricia Oliveira, Jessica Murillo-Saich, Eric Y Chang, Calen A Steiner, Paul Jedlicka, Mónica Guma, Jesús Rivera-Nieves
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Abstract

Background: Tumor necrosis factor (TNF) is a pleiotropic cytokine that plays a critical role in the pathogenesis of immune-mediated diseases including inflammatory bowel disease (IBD). The stability of its mRNA transcript, determined in part by destabilizing sequences in its AAUU repeats (ARE) gene region, is an important regulator of its tissue and systemic levels. A deletion in the ARE region of the gene resulted in IBD and arthritis in mice and pigs, supporting a critical role for the cytokine in human IBD and several human arthritides. A mutation in the same area of the mouse genome by Genentech scientists (T.Y., M.K.) resulted in a similar but not identical phenotype.

Methods: Here, we compare histopathological, cellular, and molecular features of the strains and propose reasons for their distinct phenotypes. First, while homozygous TNFΔARE mice develop severe arthritis and die after weaning, homozygous Genentech TNFΔARE (ΔG/ΔG) mice have normal lifespans, and males are often fertile.

Results: We found that while the ileitic phenotype had peaked at 12 weeks of age in all mice, colitis progressed mostly after 20 weeks of age in heterozygous mice. Their variably penetrant arthritic phenotype progressed mostly after 20 weeks, also in heterozygous mice from both strains. There was expansion of central memory T and B cells in lymphoid organs of TNF-overproducing strains and their transcriptional profile shared well-known pathogenetic pathways with human IBD. Finally, we found differences in the mutated sequences within the ARE regions of the TNF gene and in their microbiota composition and genetic background. These differences likely explain their phenotypic differences.

Conclusions: In summary, we describe a different strain of TNF-overproducing mice with an overlapping, yet not identical phenotype, which may have differential applications than the original strain.

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小鼠TNF基因中富含aauu元素的类似突变导致独特的回肠结肠炎表型:一种新的TNF过表达小鼠菌株。
背景:肿瘤坏死因子(TNF)是一种多效性细胞因子,在包括炎症性肠病(IBD)在内的免疫介导性疾病的发病机制中起关键作用。其mRNA转录物的稳定性部分由其AAUU重复序列(ARE)基因区域的不稳定序列决定,是其组织和系统水平的重要调节因子。该基因ARE区域的缺失导致小鼠和猪的IBD和关节炎,支持细胞因子在人类IBD和几种人类关节炎中的关键作用。基因泰克科学家(T.Y, M.K.)在小鼠基因组的同一区域进行了突变,导致了相似但不相同的表型。方法:在这里,我们比较了菌株的组织病理学、细胞和分子特征,并提出了它们不同表型的原因。首先,纯合子TNFΔARE小鼠会患上严重关节炎并在断奶后死亡,而纯合子Genentech TNFΔARE (ΔG/ΔG)小鼠寿命正常,而且雄性通常具有生育能力。结果:我们发现,虽然所有小鼠的回肠表型在12周龄时达到顶峰,但杂合小鼠的结肠炎主要在20周龄后进展。不同渗透性的关节炎表型在20周后主要进展,在两种菌株的杂合小鼠中也是如此。在产生tnf过量的菌株的淋巴器官中存在中央记忆T细胞和B细胞的扩增,它们的转录谱与人类IBD具有众所周知的致病途径。最后,我们发现在TNF基因的ARE区域内的突变序列及其微生物群组成和遗传背景存在差异。这些差异可能解释了它们的表型差异。结论:总之,我们描述了一种不同的具有重叠但不相同表型的tnf过量产生小鼠菌株,这可能与原始菌株有不同的应用。
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来源期刊
Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 医学-胃肠肝病学
CiteScore
9.70
自引率
6.10%
发文量
462
审稿时长
1 months
期刊介绍: Inflammatory Bowel Diseases® supports the mission of the Crohn''s & Colitis Foundation by bringing the most impactful and cutting edge clinical topics and research findings related to inflammatory bowel diseases to clinicians and researchers working in IBD and related fields. The Journal is committed to publishing on innovative topics that influence the future of clinical care, treatment, and research.
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