• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

SENP1 通过抑制 STAT3 信号转导防止压力超负荷诱导的心脏重构和功能障碍。

SENP1 Protects Against Pressure Overload-Induced Cardiac Remodeling and Dysfunction Via Inhibiting STAT3 Signaling.

机构信息

Department of Cardiology Renmin Hospital of Wuhan University Wuhan PR China.

Hubei Key Laboratory of Metabolic and Chronic Diseases Wuhan PR China.

出版信息

J Am Heart Assoc. 2022 Nov 15;11(22):e027004. doi: 10.1161/JAHA.122.027004. Epub 2022 Nov 12.

DOI:10.1161/JAHA.122.027004
PMID:36370010
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9750077/
Abstract

Background SENP1 (sentrin/small ubiquitin-like modifier-specific protease 1) has emerged as a significant modulator involved in the pathogenesis of a variety of human diseases, especially cancer. However, the regulatory roles of SENP1 in cardiovascular biology and diseases remain controversial. Our current study aims to clarify the function and regulation of SENP1 in pressure overload-induced cardiac remodeling and dysfunction. Methods and Results We used a preclinical mouse model of transverse aortic constriction coupled with in vitro studies in neonatal rat cardiomyocytes to study the role of SENP1 in cardiac hypertrophy. Gene delivery system was used to knockdown or overexpress SENP1 in vivo. Here, we observed that SENP1 expression was significantly augmented in murine hearts following transverse aortic constriction as well as neonatal rat cardiomyocytes treated with phenylephrine or angiotensin II. Cardiac-specific SENP1 knockdown markedly exacerbated transverse aortic constriction-induced cardiac hypertrophy, systolic dysfunction, fibrotic response, and cellular apoptosis. In contrast, adenovirus-mediated SENP1 overexpression in murine myocardium significantly attenuated cardiac remodeling and dysfunction following chronic pressure overload. Mechanistically, JAK2 (Janus kinase 2) and STAT3 (signal transducer and activator of transcription 3) acted as new interacting partners of SENP1 in this process. SENP1-JAK2/STAT3 interaction suppressed STAT3 nuclear translocation and activation, ultimately inhibiting the transcription of prohypertrophic genes and the initiation of hypertrophic response. Furthermore, cardiomyocyte-specific STAT3 knockout mice were generated to validate the underlying mechanisms, and the results showed that STAT3 ablation blunted the cardiac hypertrophy-promoting effects of SENP1 deficiency. Additionally, pharmacological inhibition of SENP1 by Momordin Ic amplified cardiac remodeling post-transverse aortic constriction. Conclusions Our study provided evidence that SENP1 protected against pressure overload-induced cardiac remodeling and dysfunction via inhibiting STAT3 signaling. SENP1 supplementation might constitute a new promising treatment against cardiac hypertrophy. Notably, cardiovascular side effects should be seriously considered while applying systemic SENP1 blockers to suppress tumors.

摘要

背景 SENP1(sentrin/小泛素样修饰物特异性蛋白酶 1)已成为一种重要的调节剂,参与多种人类疾病的发病机制,尤其是癌症。然而,SENP1 在心血管生物学和疾病中的调节作用仍存在争议。我们目前的研究旨在阐明 SENP1 在压力超负荷诱导的心脏重构和功能障碍中的作用和调节机制。

方法和结果 我们使用了一种结合了在体研究的转基因小鼠模型和新生大鼠心肌细胞的方法,来研究 SENP1 在心肌肥厚中的作用。基因传递系统用于在体内敲低或过表达 SENP1。在此,我们观察到在横主动脉缩窄后的小鼠心脏以及用苯肾上腺素或血管紧张素 II 处理的新生大鼠心肌细胞中,SENP1 的表达显著增加。心脏特异性 SENP1 敲低显著加剧了横主动脉缩窄诱导的心脏肥厚、收缩功能障碍、纤维化反应和细胞凋亡。相比之下,腺病毒介导的 SENP1 在小鼠心肌中的过表达显著减轻了慢性压力超负荷后的心脏重构和功能障碍。在机制上,JAK2(Janus 激酶 2)和 STAT3(信号转导和转录激活因子 3)作为 SENP1 在该过程中的新相互作用伙伴发挥作用。SENP1-JAK2/STAT3 相互作用抑制了 STAT3 的核转位和激活,最终抑制了促肥厚基因的转录和肥厚反应的启动。此外,还生成了心肌细胞特异性 STAT3 敲除小鼠以验证潜在机制,结果表明 STAT3 缺失削弱了 SENP1 缺乏对心脏肥厚的促进作用。此外,Momordin Ic 通过抑制 SENP1 抑制了横主动脉缩窄后的心脏重构。

结论 我们的研究提供了证据表明,SENP1 通过抑制 STAT3 信号来防止压力超负荷诱导的心脏重构和功能障碍。SENP1 的补充可能成为一种针对心肌肥厚的新的有前途的治疗方法。值得注意的是,在应用全身性 SENP1 抑制剂来抑制肿瘤时,应认真考虑心血管副作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1cb/9750077/2507eadeaf1b/JAH3-11-e027004-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1cb/9750077/b6bd0f540a8d/JAH3-11-e027004-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1cb/9750077/bc652d2a49ab/JAH3-11-e027004-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1cb/9750077/6910c53c90f3/JAH3-11-e027004-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1cb/9750077/916fcb5b3c89/JAH3-11-e027004-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1cb/9750077/4b87efc0a4c6/JAH3-11-e027004-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1cb/9750077/8de1b8333acc/JAH3-11-e027004-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1cb/9750077/f975030c0b7b/JAH3-11-e027004-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1cb/9750077/2507eadeaf1b/JAH3-11-e027004-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1cb/9750077/b6bd0f540a8d/JAH3-11-e027004-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1cb/9750077/bc652d2a49ab/JAH3-11-e027004-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1cb/9750077/6910c53c90f3/JAH3-11-e027004-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1cb/9750077/916fcb5b3c89/JAH3-11-e027004-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1cb/9750077/4b87efc0a4c6/JAH3-11-e027004-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1cb/9750077/8de1b8333acc/JAH3-11-e027004-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1cb/9750077/f975030c0b7b/JAH3-11-e027004-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1cb/9750077/2507eadeaf1b/JAH3-11-e027004-g008.jpg

相似文献

1
SENP1 Protects Against Pressure Overload-Induced Cardiac Remodeling and Dysfunction Via Inhibiting STAT3 Signaling.SENP1 通过抑制 STAT3 信号转导防止压力超负荷诱导的心脏重构和功能障碍。
J Am Heart Assoc. 2022 Nov 15;11(22):e027004. doi: 10.1161/JAHA.122.027004. Epub 2022 Nov 12.
2
Interleukin-10 treatment attenuates pressure overload-induced hypertrophic remodeling and improves heart function via signal transducers and activators of transcription 3-dependent inhibition of nuclear factor-κB.白细胞介素-10 治疗通过信号转导和转录激活因子 3 依赖性核因子-κB 的抑制来减轻压力超负荷诱导的心肌肥厚重塑,改善心脏功能。
Circulation. 2012 Jul 24;126(4):418-29. doi: 10.1161/CIRCULATIONAHA.112.112185. Epub 2012 Jun 15.
3
Leucine zipper protein 1 attenuates pressure overload-induced cardiac hypertrophy through inhibiting Stat3 signaling.亮氨酸拉链蛋白 1 通过抑制 Stat3 信号通路减轻压力超负荷诱导的心肌肥厚。
J Adv Res. 2024 Sep;63:117-128. doi: 10.1016/j.jare.2023.10.007. Epub 2023 Oct 6.
4
Mnk1 (Mitogen-Activated Protein Kinase-Interacting Kinase 1) Deficiency Aggravates Cardiac Remodeling in Mice.Mnk1(丝裂原活化蛋白激酶相互作用激酶1)缺乏加重小鼠心脏重塑。
Hypertension. 2016 Dec;68(6):1393-1399. doi: 10.1161/HYPERTENSIONAHA.116.07906. Epub 2016 Oct 3.
5
SH2B1 is critical for the regulation of cardiac remodelling in response to pressure overload.SH2B1 对于心脏重构在应对压力超负荷时的调节至关重要。
Cardiovasc Res. 2015 Jul 15;107(2):203-15. doi: 10.1093/cvr/cvv170. Epub 2015 Jun 15.
6
The functional role of m6A demethylase ALKBH5 in cardiomyocyte hypertrophy.ALKBH5 在心肌细胞肥大中的功能作用。
Cell Death Dis. 2024 Sep 18;15(9):683. doi: 10.1038/s41419-024-07053-2.
7
SENP1-Mediated HSP90ab1 DeSUMOylation in Cardiomyocytes Prevents Myocardial Fibrosis by Paracrine Signaling.SENP1 介导的心肌细胞 HSP90ab1 的去 SUMOylation 通过旁分泌信号防止心肌纤维化。
Adv Sci (Weinh). 2024 Sep;11(34):e2400741. doi: 10.1002/advs.202400741. Epub 2024 Jul 11.
8
6-Gingerol protects against cardiac remodeling by inhibiting the p38 mitogen-activated protein kinase pathway.6-姜酚通过抑制 p38 丝裂原活化蛋白激酶通路保护心脏重构。
Acta Pharmacol Sin. 2021 Oct;42(10):1575-1586. doi: 10.1038/s41401-020-00587-z. Epub 2021 Jan 18.
9
Postnatal Deletion of Bmal1 in Cardiomyocyte Promotes Pressure Overload Induced Cardiac Remodeling in Mice.心肌细胞中 Bmal1 的产后缺失促进小鼠压力超负荷诱导的心脏重构。
J Am Heart Assoc. 2022 Jul 5;11(13):e025021. doi: 10.1161/JAHA.121.025021. Epub 2022 Jun 22.
10
C1q-TNF-related protein-3 attenuates pressure overload-induced cardiac hypertrophy by suppressing the p38/CREB pathway and p38-induced ER stress.C1q-TNF 相关蛋白-3 通过抑制 p38/CREB 通路和 p38 诱导的内质网应激来减轻压力超负荷诱导的心肌肥厚。
Cell Death Dis. 2019 Jul 8;10(7):520. doi: 10.1038/s41419-019-1749-0.

引用本文的文献

1
Fumarate hydratase ameliorates pressure overload induced cardiac remodeling by controlling Elovl7-mediated biosynthesis of unsaturated fatty acids.延胡索酸水合酶通过控制Elovl7介导的不饱和脂肪酸生物合成来改善压力超负荷诱导的心脏重塑。
Acta Pharmacol Sin. 2025 Sep 12. doi: 10.1038/s41401-025-01637-0.
2
SENP1: A perspective from immune cells to disease (Review).SENP1:从免疫细胞到疾病的视角(综述)。
Oncol Rep. 2025 Sep;54(3). doi: 10.3892/or.2025.8947. Epub 2025 Jul 19.
3
The multifaceted nature of SUMOylation in heart disease and its therapeutic potential.

本文引用的文献

1
Recent research and development of inhibitors targeting sentrin-specific protease 1 for the treatment of cancers.针对 Sntn 特异性蛋白酶 1 的抑制剂的最新研究与开发用于癌症治疗。
Eur J Med Chem. 2022 Nov 5;241:114650. doi: 10.1016/j.ejmech.2022.114650. Epub 2022 Aug 1.
2
Neuraminidase 1 deficiency attenuates cardiac dysfunction, oxidative stress, fibrosis, inflammatory via AMPK-SIRT3 pathway in diabetic cardiomyopathy mice.神经氨酸酶 1 缺乏通过 AMPK-SIRT3 通路减轻糖尿病心肌病小鼠的心功能障碍、氧化应激、纤维化和炎症。
Int J Biol Sci. 2022 Jan 1;18(2):826-840. doi: 10.7150/ijbs.65938. eCollection 2022.
3
SUMO-specific Isopeptidases Tuning Cardiac SUMOylation in Health and Disease.
SUMO化修饰在心脏病中的多面性及其治疗潜力。
Mol Cell Biochem. 2025 Apr 27. doi: 10.1007/s11010-025-05286-z.
4
Mineralocorticoid Receptor Blocker Prevents Mineralocorticoid Receptor-Mediated Inflammation by Modulating Transcriptional Activity of Mineralocorticoid Receptor-p65-Signal Transducer and Activator of Transcription 3 Complex.醛固酮受体阻滞剂通过调节醛固酮受体-p65-信号转导和转录激活因子 3 复合物的转录活性来预防醛固酮受体介导的炎症。
J Am Heart Assoc. 2024 Sep 17;13(18):e030941. doi: 10.1161/JAHA.123.030941. Epub 2024 Sep 9.
5
SENP1-Mediated HSP90ab1 DeSUMOylation in Cardiomyocytes Prevents Myocardial Fibrosis by Paracrine Signaling.SENP1 介导的心肌细胞 HSP90ab1 的去 SUMOylation 通过旁分泌信号防止心肌纤维化。
Adv Sci (Weinh). 2024 Sep;11(34):e2400741. doi: 10.1002/advs.202400741. Epub 2024 Jul 11.
6
Macrod1 suppresses diabetic cardiomyopathy via regulating PARP1-NAD-SIRT3 pathway.Macrod1 通过调节 PARP1-NAD-SIRT3 通路抑制糖尿病心肌病。
Acta Pharmacol Sin. 2024 Jun;45(6):1175-1188. doi: 10.1038/s41401-024-01247-2. Epub 2024 Mar 8.
7
SUMOylation of TEAD1 Modulates the Mechanism of Pathological Cardiac Hypertrophy.SUMOylation 修饰 TEAD1 调节病理性心肌肥厚的机制。
Adv Sci (Weinh). 2024 Mar;11(12):e2305677. doi: 10.1002/advs.202305677. Epub 2024 Jan 15.
8
Leucine zipper protein 1 attenuates pressure overload-induced cardiac hypertrophy through inhibiting Stat3 signaling.亮氨酸拉链蛋白 1 通过抑制 Stat3 信号通路减轻压力超负荷诱导的心肌肥厚。
J Adv Res. 2024 Sep;63:117-128. doi: 10.1016/j.jare.2023.10.007. Epub 2023 Oct 6.
小泛素样修饰特异性异肽酶在健康与疾病中调节心脏小泛素样修饰
Front Mol Biosci. 2021 Nov 19;8:786136. doi: 10.3389/fmolb.2021.786136. eCollection 2021.
4
β-Cell Knockout of SENP1 Reduces Responses to Incretins and Worsens Oral Glucose Tolerance in High-Fat Diet-Fed Mice.β细胞中 SENP1 的敲除减少了对肠降血糖素的反应,并加重了高脂肪饮食喂养小鼠的口服葡萄糖耐量异常。
Diabetes. 2021 Nov;70(11):2626-2638. doi: 10.2337/db20-1235. Epub 2021 Aug 30.
5
Role of the SENP1-SIRT1 pathway in hyperoxia-induced alveolar epithelial cell injury.SENP1-SIRT1 通路在高氧诱导的肺泡上皮细胞损伤中的作用。
Free Radic Biol Med. 2021 Sep;173:142-150. doi: 10.1016/j.freeradbiomed.2021.07.027. Epub 2021 Jul 24.
6
Evidence of Omics, Immune Infiltration, and Pharmacogenomic for SENP1 in the Pan-Cancer Cohort.泛癌队列中SENP1的组学、免疫浸润和药物基因组学证据。
Front Pharmacol. 2021 Jul 1;12:700454. doi: 10.3389/fphar.2021.700454. eCollection 2021.
7
Glucose limitation activates AMPK coupled SENP1-Sirt3 signalling in mitochondria for T cell memory development.葡萄糖限制激活 AMPK 偶联 SENP1-Sirt3 信号通路在 T 细胞记忆发育中的作用。
Nat Commun. 2021 Jul 16;12(1):4371. doi: 10.1038/s41467-021-24619-2.
8
PKM1 Exerts Critical Roles in Cardiac Remodeling Under Pressure Overload in the Heart.PKM1 在心脏压力超负荷下的心脏重构中发挥关键作用。
Circulation. 2021 Aug 31;144(9):712-727. doi: 10.1161/CIRCULATIONAHA.121.054885. Epub 2021 Jun 9.
9
Sorting nexin 3 induces heart failure via promoting retromer-dependent nuclear trafficking of STAT3.分选连接蛋白 3 通过促进 STAT3 依赖于逆行体的核转位诱导心力衰竭。
Cell Death Differ. 2021 Oct;28(10):2871-2887. doi: 10.1038/s41418-021-00789-w. Epub 2021 May 4.
10
SUMOylation controls the binding of hexokinase 2 to mitochondria and protects against prostate cancer tumorigenesis.SUMOylation 控制己糖激酶 2 与线粒体的结合,防止前列腺癌发生。
Nat Commun. 2021 Mar 22;12(1):1812. doi: 10.1038/s41467-021-22163-7.