通过激活TGF-β/SMAD信号通路,UHRF1促进表皮-介质细胞过渡,从而调解纤维化
Lijie Yang1, Penghui Si1,2, Tuoheti Kuerban1
1Department of Urology, Zhongnan Hospital of Wuhan University, Wuhan, 430071, China.
Scientific reports
|January 27, 2025
概括
通过TGF-β/SMAD通路,UHRF1的上调加速纤维化和上皮-介质细胞过渡 (EMT). 欣诺基可以通过抑制UHRF1表达来预防纤维化.
科学领域:
- 腎臟病學 (nephrology) 是一種醫學專業.
- 分子生物学分子生物学
- 表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.
背景情况:
- 纤维化是慢性病的常见结果.
- 表皮-介质细胞过渡 (EMT) 驱动损伤后纤维化进展.
- 在纤维化和EMT中UHRF1的作用需要阐明.
研究的目的:
- 研究UHRF1在纤维化和EMT中的作用.
- 评估Hinokitiol在预防纤维化方面的潜力.
主要方法:
- 分析了GEO和Nephroseq数据库数据.
- 使用TGF-β1刺激的HK2细胞和UUO/叶酸诱导的动物模型.
- 执行UHRF1敲击并用Hinokitiol进行治疗.
主要成果:
- 在纤维化模型中,UHRF1的表达高.
- 抑制UHRF1 knockdown抑制了TGF-β/SMAD信号传递,减少了EMT,并减弱了纤维化.
- 欣诺基抑制了UHRF1,改善了EMT,并通过抑制SMAD2/3酸化来减少纤维化.
结论:
- 上调的UHRF1通过TGF-β/SMAD通路加速管细胞EMT和纤维化.
- 欣诺基醇通过降低UHRF1.1的调节,显示出改善纤维化的潜力.
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