下调和上调
包装D1
基因敲除
癌症研究
组蛋白H3
常染色体显性多囊肾病
组蛋白
纤维化
多囊肾病
内科学
内分泌学
生物
肾
医学
基因
遗传学
作者
Xiaoyan Li,Lu Zhang,Ewud Agborbesong,Xiaoqin Zhang,Julie Zhou,Xiaogang Li
出处
期刊:American Journal of Physiology-renal Physiology
[American Physiological Society]
日期:2022-06-27
卷期号:323 (2): F227-F242
被引量:20
标识
DOI:10.1152/ajprenal.00452.2021
摘要
Here, we identified a cross talk between SET and MYND domain-containing lysine methyltransferase 2 (Smyd2) and transforming growth factor (TGF)-β-Smad3 signaling and a synergistic feedback loop between them, in which TGF-β stimulates expression of Smyd2 in a Smad3-dependent manner, and upregulation of Smyd2 regulates the transcription of TGF-β and other fibrotic marker genes through direct binding on their promoters or methylating histone H3 indirectly to regulate the transcription of those genes in fibroblasts. Thus, the Smyd2-TGF-β-Smad3-Smyd2 signaling axis plays an important role in promoting renal fibrosis, and targeting Smyd2 with its specific inhibitor should not only delay cyst growth but also ameliorate renal fibrosis in ADPKD.
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