• 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

E3泛素连接酶TRIM2被鉴定为CYP11B2和醛固酮生成的新型抑制因子。

E3 ubiquitin ligase TRIM2 identified as a novel suppressor of CYP11B2 and aldosterone production.

作者信息

Chen Liang, Hu Xuan, Wang Gang, Yu Fang, Dai Zhe, Jian Xiaobin, Li Yong, Xiang Wan, Meng Zhe

机构信息

Department of Urology, Zhongnan Hospital of Wuhan University, Wuhan, China.

Hubei Key Laboratory of Urological Diseases, Wuhan, China.

出版信息

Cell Mol Life Sci. 2024 Dec 27;82(1):27. doi: 10.1007/s00018-024-05545-0.

DOI:10.1007/s00018-024-05545-0
PMID:39725733
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11671668/
Abstract

Aldosterone-producing adenoma (APA) is a leading cause of primary aldosteronism (PA), a condition marked by excessive aldosterone secretion. CYP11B2, the aldosterone synthase, plays a critical role in aldosterone biosynthesis and the development of APA. Despite its significance, encoding regulatory mechanisms governing CYP11B2, particularly its degradation, remain poorly understood. In this study, we sought to uncover novel regulators of CYP11B2 stability by conducting a siRNA screen targeting E3 ubiquitin ligases. Our results identified TRIM2 as a key negative regulator of CYP11B2, where its overexpression led to a significant reduction in CYP11B2 protein levels and a concomitant decrease in aldosterone production in adrenal tumor cells. Mechanistically, we demonstrated that TRIM2 interacts with CYP11B2 via its RBCC domain, promoting K29/48-linked polyubiquitination and destabilization of CYP11B2. Further results revealed that TRIM2 is downregulated in APA tissues, showing differential expression between the zona glomerulosa (ZG) and zona fasciculata (ZF) of normal adrenal tissue. These findings highlight TRIM2 as a novel modulator of aldosterone synthesis through CYP11B2 degradation, offering a potential therapeutic target for APA.

摘要

醛固酮分泌性腺瘤(APA)是原发性醛固酮增多症(PA)的主要病因,PA的特征是醛固酮分泌过多。醛固酮合成酶CYP11B2在醛固酮生物合成和APA的发生发展中起关键作用。尽管其具有重要意义,但调控CYP11B2的编码机制,尤其是其降解机制,仍知之甚少。在本研究中,我们通过针对E3泛素连接酶进行小干扰RNA筛选,试图发现CYP11B2稳定性的新调节因子。我们的结果确定TRIM2是CYP11B2的关键负调节因子,其过表达导致肾上腺肿瘤细胞中CYP11B2蛋白水平显著降低,同时醛固酮分泌减少。从机制上讲,我们证明TRIM2通过其RBCC结构域与CYP11B2相互作用,促进K29/48连接的多聚泛素化和CYP11B2的不稳定。进一步的结果显示,TRIM2在APA组织中表达下调,在正常肾上腺组织的球状带(ZG)和束状带(ZF)之间表现出差异表达。这些发现突出了TRIM2作为通过CYP11B2降解调节醛固酮合成的新调节因子,为APA提供了一个潜在的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e990/11671668/6420cb272112/18_2024_5545_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e990/11671668/14429e4b60e4/18_2024_5545_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e990/11671668/2791b7cacf3e/18_2024_5545_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e990/11671668/bb91120d168a/18_2024_5545_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e990/11671668/bff262bcb76e/18_2024_5545_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e990/11671668/f0a44a75b74a/18_2024_5545_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e990/11671668/6420cb272112/18_2024_5545_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e990/11671668/14429e4b60e4/18_2024_5545_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e990/11671668/2791b7cacf3e/18_2024_5545_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e990/11671668/bb91120d168a/18_2024_5545_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e990/11671668/bff262bcb76e/18_2024_5545_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e990/11671668/f0a44a75b74a/18_2024_5545_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e990/11671668/6420cb272112/18_2024_5545_Fig6_HTML.jpg

相似文献

1
E3 ubiquitin ligase TRIM2 identified as a novel suppressor of CYP11B2 and aldosterone production.E3泛素连接酶TRIM2被鉴定为CYP11B2和醛固酮生成的新型抑制因子。
Cell Mol Life Sci. 2024 Dec 27;82(1):27. doi: 10.1007/s00018-024-05545-0.
2
ABCC3 Is a Differential Marker of CYP11B2-Negative Zona Glomerulosa Cells in Human Adrenal Cortex.ABCC3是人类肾上腺皮质中CYP11B2阴性肾小球带细胞的差异标志物。
Endocr Pathol. 2025 May 7;36(1):17. doi: 10.1007/s12022-025-09862-3.
3
Adrenal cortex remodeling and functional zona glomerulosa hyperplasia in primary aldosteronism.原发性醛固酮增多症中的肾上腺皮质重塑和功能球状带增生。
Hypertension. 2010 Nov;56(5):885-92. doi: 10.1161/HYPERTENSIONAHA.110.158543. Epub 2010 Oct 11.
4
Zona Glomerulosa-Derived Klotho Modulates Aldosterone Synthase Expression in Young Female Mice.肾小球带衍生的 Klotho 调节年轻雌性小鼠醛固酮合酶的表达。
Endocrinology. 2024 Mar 29;165(5). doi: 10.1210/endocr/bqae040.
5
Quantitative assessment of CYP11B1 and CYP11B2 expression in aldosterone-producing adenomas.醛固酮分泌性腺瘤中CYP11B1和CYP11B2表达的定量评估。
Eur J Endocrinol. 2002 Dec;147(6):795-802. doi: 10.1530/eje.0.1470795.
6
YM750, an ACAT Inhibitor, Acts on Adrenocortical Cells to Inhibit Aldosterone Secretion Due to Depolarization.YM750,一种 ACAT 抑制剂,通过去极化作用作用于肾上腺皮质细胞,抑制醛固酮分泌。
Int J Mol Sci. 2022 Oct 24;23(21):12803. doi: 10.3390/ijms232112803.
7
Chronic activation of adrenal Gq signaling induces Cyp11b2 expression in the zona fasciculata and hyperaldosteronism.肾上腺 Gq 信号的慢性激活诱导zona fasciculata 中 Cyp11b2 的表达和醛固酮增多症。
Mol Cell Endocrinol. 2024 May 1;585:112176. doi: 10.1016/j.mce.2024.112176. Epub 2024 Feb 8.
8
Evaluating the role of aldosterone synthesis on adrenal cell fate.评估醛固酮合成对肾上腺细胞命运的作用。
Front Endocrinol (Lausanne). 2024 Aug 7;15:1423027. doi: 10.3389/fendo.2024.1423027. eCollection 2024.
9
The angiotensin type 2 receptor in the human adrenocortical zona glomerulosa and in aldosterone-producing adenoma: low expression and no functional role.人类肾上腺球状带中的血管紧张素 2 型受体和醛固酮分泌腺瘤:低表达和无功能作用。
Clin Sci (Lond). 2018 Mar 20;132(6):627-640. doi: 10.1042/CS20171593. Print 2018 Mar 30.
10
PCP4: a regulator of aldosterone synthesis in human adrenocortical tissues.PCP4:人肾上腺皮质组织中醛固酮合成的调节剂。
J Mol Endocrinol. 2014 Feb 24;52(2):159-67. doi: 10.1530/JME-13-0248. Print 2014 Apr.

本文引用的文献

1
Targeting the Renin-angiotensin-aldosterone System (RAAS) for Cardiovascular Protection and Enhanced Oncological Outcomes: Review.靶向肾素-血管紧张素-醛固酮系统(RAAS)以保护心血管和改善肿瘤学结局:综述。
Curr Treat Options Oncol. 2024 Nov;25(11):1406-1427. doi: 10.1007/s11864-024-01270-9. Epub 2024 Oct 18.
2
Hypoxia-induced PLOD2 promotes clear cell renal cell carcinoma progression via modulating EGFR-dependent AKT pathway activation.缺氧诱导的 PLOD2 通过调节 EGFR 依赖性 AKT 通路激活促进肾透明细胞癌进展。
Cell Death Dis. 2023 Nov 27;14(11):774. doi: 10.1038/s41419-023-06298-7.
3
Bacterial Cytochrome P450 Catalyzed Post-translational Macrocyclization of Ribosomal Peptides.
细菌细胞色素 P450 催化核糖体肽的翻译后大环化。
Angew Chem Int Ed Engl. 2023 Nov 13;62(46):e202311533. doi: 10.1002/anie.202311533. Epub 2023 Oct 13.
4
NRP1 promotes prostate cancer progression via modulating EGFR-dependent AKT pathway activation.NRP1 通过调节 EGFR 依赖性 AKT 通路激活促进前列腺癌进展。
Cell Death Dis. 2023 Feb 25;14(2):159. doi: 10.1038/s41419-023-05696-1.
5
Engineering Cytochrome P450BM3 Enzymes for Direct Nitration of Unsaturated Hydrocarbons.用于不饱和烃直接硝化的工程化细胞色素P450BM3酶
Angew Chem Int Ed Engl. 2023 Mar 20;62(13):e202217678. doi: 10.1002/anie.202217678. Epub 2023 Feb 6.
6
Control of protein stability by post-translational modifications.蛋白质翻译后修饰对其稳定性的调控。
Nat Commun. 2023 Jan 13;14(1):201. doi: 10.1038/s41467-023-35795-8.
7
Phosphorylation of CaMK and CREB-Mediated Cardiac Aldosterone Synthesis Induced by Arginine Vasopressin in Rats with Myocardial Infarction.血管加压素诱导心肌梗死后大鼠 CaMK 和 CREB 介导的心脏醛固酮合成的磷酸化。
Int J Mol Sci. 2022 Dec 1;23(23):15061. doi: 10.3390/ijms232315061.
8
Primary aldosteronism - a multidimensional syndrome.原发性醛固酮增多症——一种多维综合征。
Nat Rev Endocrinol. 2022 Nov;18(11):665-682. doi: 10.1038/s41574-022-00730-2. Epub 2022 Aug 31.
9
Diagnosis and treatment of primary aldosteronism.原发性醛固酮增多症的诊断与治疗。
Lancet Diabetes Endocrinol. 2021 Dec;9(12):876-892. doi: 10.1016/S2213-8587(21)00210-2.
10
Major advances in targeted protein degradation: PROTACs, LYTACs, and MADTACs.靶向蛋白降解的主要进展:PROTACs、LYTACs 和 MADTACs。
J Biol Chem. 2021 Jan-Jun;296:100647. doi: 10.1016/j.jbc.2021.100647. Epub 2021 Apr 9.