SPDEF通过NR4A1的转录激活改善uuo诱导的肾纤维化。

IF 6 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Medicine Pub Date : 2024-12-30 DOI:10.1186/s10020-024-01030-3
Hongshuang Wang, Ziheng Wei, Chang Xu, Fang Fang, Zheng Wang, Yan Zhong, Xiangting Wang
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引用次数: 0

摘要

核受体4A1 (NR4A1)是一个增加慢性肾脏疾病(CKD)的可能性并促进其发展的基因。先前的研究表明,含有Ets转化特异性转录因子(SPDEF)的SAM点结构域可以激活NR4A1,但其在肾纤维化中的作用机制尚不清楚。在这项研究中,我们使用腺病毒建立了具有特异性敲低NR4A1基因的小鼠肾脏模型。我们的研究结果表明,NR4A1的下调可加速单侧输尿管梗阻(UUO)诱导的小鼠肾纤维化,NR4A1的过表达可显著降低HK-2细胞中转化生长因子-β1 (TGF-β1)诱导的纤维化。此外,我们发现过表达SPDEF可以通过转录激活NR4A1改善uuo诱导的小鼠肾纤维化和TGF-β1诱导的HK-2纤维化。这些发现表明SPDEF可以通过转录激活NR4A1并改善肾纤维化。
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SPDEF ameliorates UUO-induced renal fibrosis by transcriptional activation of NR4A1.

Nuclear receptor 4A1 (NR4A1) is a gene that increases the likelihood of chronic kidney disease (CKD) and contributes to its development. Previous research has shown that the SAM pointed domain containing Ets transformation-specific transcription factor (SPDEF) can activate NR4A1, but its mechanism of action in renal fibrosis is not yet clear. In this study, we used adenovirus to create a mouse kidney model with a specific knockdown of NR4A1 gene. Our results showed that the knockdown of NR4A1 can accelerate unilateral ureteral obstruction (UUO)-induced renal fibrosis in mice, and overexpression of NR4A1 can significantly reduce transforming growth factor-β1-induced (TGF-β1) fibrosis in HK-2 cells. Additionally, we found that overexpression of SPDEF can improve UUO-induced renal fibrosis in mice and TGF-β1-induced fibrosis in HK-2 by transcriptionally activating NR4A1. These findings suggest that SPDEF can activate NR4A1 transcriptionally and improve renal fibrosis.

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来源期刊
Molecular Medicine
Molecular Medicine 医学-生化与分子生物学
CiteScore
8.60
自引率
0.00%
发文量
137
审稿时长
1 months
期刊介绍: Molecular Medicine is an open access journal that focuses on publishing recent findings related to disease pathogenesis at the molecular or physiological level. These insights can potentially contribute to the development of specific tools for disease diagnosis, treatment, or prevention. The journal considers manuscripts that present material pertinent to the genetic, molecular, or cellular underpinnings of critical physiological or disease processes. Submissions to Molecular Medicine are expected to elucidate the broader implications of the research findings for human disease and medicine in a manner that is accessible to a wide audience.
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