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与炎症性肠道疾病相关的SNP增加了局部甲状腺蛋白的表达,从而在微型大犬中发展炎症
Yong Bin Teoh1,2, Jing-Jing Jiang1, Takeshi Yamasaki1,3
1Division of Molecular Psychoneuroimmunology, Institute for Genetic Medicine, Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
Frontiers in veterinary science
|July 31, 2023
概括
一种特定的基因变异 (TG c.4567C>T) 增加了微型大公犬炎症性结直肠多体 (ICRP) 的风险. 这种基因变化会影响TG表达,激活可能成为治疗点的炎症途径.
科学领域:
- 兽医遗传学 兽医遗传学
- 胃肠病学 胃肠病学
- 免疫学 免疫学 免疫学
背景情况:
- 迷你大公犬的炎症性结直肠多 (ICRP) 是一种慢性疾病.
- 之前的研究已经确定了与ICRP相关的五种单核酸多态 (SNP).
- 该TG基因是被确定可能与ICRP相关的基因之一.
研究的目的:
- 为了研究TG c.4567C>T SNP和ICRP在微型大犬中的关联.
- 探索TG在IL-6放大器通路中的作用.
- 为了确定TG是否是ICRP的诊断或治疗目标.
主要方法:
- 微型大犬的基因定型为TG c.4567C>T SNP.
- 在体外实验评估TG表达及其对IL-6放大器的影响.
- 从受影响和未受影响的狗的结肠样本中分析TG,IL6和CCL2表达.
主要成果:
- TG c.4567C>T 的T/T 风险等位基因在具有ICRP的犬中明显更频繁.
- TG表达由IL-6和TNF-α上调,而TG缺乏抑制IL-6放大器.
- 重组TG增强了IL-6放大器激活,表明TG是一个正调节器.
- 在具有T/T风险等位基因的结肠组织中观察到TG,IL6和CCL2表达的增加.
结论:
- TG c.4567C>T SNP 作为结肠中TG mRNA的表达定量特征位置 (eQTL).
- 这种SNP驱动的局部TG表达通过IL-6放大器增加了微型大犬的ICRP风险.
- TG c.4567C>T是一种潜在的诊断标记,TG介导的IL-6放大器激活是ICRP的潜在治疗标.
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