JOSD2通过去泛素化和稳定SMAD7抑制血管紧张素ii诱导的血管重构。

IF 6.9 1区 医学 Q1 CHEMISTRY, MULTIDISCIPLINARY Acta Pharmacologica Sinica Pub Date : 2025-01-20 DOI:10.1038/s41401-024-01437-y
Si-Rui Shen, Zhu-Qi Huang, Yu-Die Yang, Ji-Bo Han, Zi-Min Fang, Yue Guan, Jia-Chen Xu, Ju-Lian Min, Yi Wang, Gao-Jun Wu, Zhong-Xiang Xiao, Wu Luo, Zhou-Qing Huang, Guang Liang
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引用次数: 0

摘要

血管紧张素II (Ang II)水平的升高在高血压血管重构的发展中起着核心作用。在本研究中,我们确定了去泛素化酶Josephin domain-containing protein 2 (JOSD2)作为一种保护因子,并研究了其在Ang ii诱导的血管重构中的分子机制。首先,我们发现JOSD2在angii挑战小鼠血管组织的主动脉平滑肌细胞中上调,而在内皮细胞中不上调。全身敲除JOSD2显著恶化了angii诱导的小鼠血管重构。相反,Ang ii诱导的血管重构被血管平滑肌细胞(VSMC)特异性JOSD2过表达逆转。在体外,JOSD2缺乏加剧了Ang ii诱导的VSMCs的纤维化、增殖和迁移,而这些变化被JOSD2过表达逆转。RNA-seq分析显示,JOSD2对VSMCs的保护作用与tgf - β- smad通路有关。此外,LC-MS/MS分析发现tgf - β- smad通路中的负调节因子SMAD7是JOSD2的底物。JOSD2特异性结合到SMAD7的MH1结构域,在赖氨酸220位点移除SMAD7上k48连接的泛素链,以维持SMAD7的稳定性。综上所述,我们的发现表明JOSD2- smad7轴对缓解angii诱导的血管重构至关重要,JOSD2可能是高血压血管重构的一个新的潜在治疗靶点。
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JOSD2 inhibits angiotensin II-induced vascular remodeling by deubiquitinating and stabilizing SMAD7.

Increased level of angiotensin II (Ang II) plays a central role in the development of hypertensive vascular remodeling. In this study, we identified the deubiquitinating enzyme Josephin domain-containing protein 2 (JOSD2) as a protective factor and investigated its molecular mechanism in Ang II-induced vascular remodeling. First, we found that JOSD2 was upregulated in aortic smooth muscle cells, but not in endothelial cells of Ang II-challenged mouse vascular tissues. Whole-body knockout of JOSD2 significantly deteriorated Ang II-induced vascular remodeling in mice. Conversely, Ang II-induced vascular remodeling was reversed by vascular smooth muscle cell (VSMC)-specific JOSD2 overexpression. In vitro, JOSD2 deficiency aggravated Ang II-induced fibrosis, proliferation, and migration VSMCs, while these changes were reversed by JOSD2 overexpression. RNA-seq analysis showed that the protective effects of JOSD2 in VSMCs were related to the TGFβ-SMAD pathway. Furthermore, the LC-MS/MS analysis identified SMAD7, a negative regulator in the TGFβ-SMAD pathway, as the substrate of JOSD2. JOSD2 specifically bound to the MH1 domain of SMAD7 to remove the K48-linked ubiquitin chains from SMAD7 at lysine 220 to sustain SMAD7 stability. Taken together, our finding reveals that the JOSD2-SMAD7 axis is critical for relieving Ang II-induced vascular remodeling and JOSD2 may be a novel and potential therapeutic target for hypertensive vascular remodeling.

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来源期刊
Acta Pharmacologica Sinica
Acta Pharmacologica Sinica 医学-化学综合
CiteScore
15.10
自引率
2.40%
发文量
4365
审稿时长
2 months
期刊介绍: APS (Acta Pharmacologica Sinica) welcomes submissions from diverse areas of pharmacology and the life sciences. While we encourage contributions across a broad spectrum, topics of particular interest include, but are not limited to: anticancer pharmacology, cardiovascular and pulmonary pharmacology, clinical pharmacology, drug discovery, gastrointestinal and hepatic pharmacology, genitourinary, renal, and endocrine pharmacology, immunopharmacology and inflammation, molecular and cellular pharmacology, neuropharmacology, pharmaceutics, and pharmacokinetics. Join us in sharing your research and insights in pharmacology and the life sciences.
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