• 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

RhoA/ROCK1/YAP/F-肌动蛋白的下调导致主动脉平滑肌细胞硬度降低,促进主动脉夹层形成。

Downregulation of RhoA/ROCK1/YAP/F-actin causing decreased aortic smooth muscle cell stiffness promotes aortic dissection formation.

作者信息

Zhang Wei, Wang Mengxiao, Wang Enci, Lu Wei, Li Zengxia, Zhang Yuchong, Hu Gaofei, Zhang Qi, Shan Wenxin, Dang Yongjun, Zhao Zhe, Zheng Lemin, Fu Weiguo, Wang Lixin

机构信息

Department of Vascular Surgery, Zhongshan Hospital, Fudan University, Shanghai 200032, China.

Vascular Surgery Institute, Zhongshan Hospital, Fudan University, Shanghai 200032, China.

出版信息

Life Metab. 2024 Jun 3;3(5):loae022. doi: 10.1093/lifemeta/loae022. eCollection 2024 Oct.

DOI:10.1093/lifemeta/loae022
PMID:39872140
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11749839/
Abstract

Downregulated RhoA/ROCK1/YAP/F-actin axis leads to decreased AoSMC stiffness and promotes AD formation.

摘要

RhoA/ROCK1/YAP/丝状肌动蛋白轴下调导致主动脉平滑肌细胞硬度降低并促进主动脉夹层形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48b1/11749839/36f0cc5f0146/loae022_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48b1/11749839/6076f9bb20b1/loae022_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48b1/11749839/36f0cc5f0146/loae022_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48b1/11749839/6076f9bb20b1/loae022_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48b1/11749839/36f0cc5f0146/loae022_fig1.jpg

相似文献

1
Downregulation of RhoA/ROCK1/YAP/F-actin causing decreased aortic smooth muscle cell stiffness promotes aortic dissection formation.RhoA/ROCK1/YAP/F-肌动蛋白的下调导致主动脉平滑肌细胞硬度降低,促进主动脉夹层形成。
Life Metab. 2024 Jun 3;3(5):loae022. doi: 10.1093/lifemeta/loae022. eCollection 2024 Oct.
2
Yap-Hippo pathway regulates cerebral hypoxia-reoxygenation injury in neuroblastoma N2a cells via inhibiting ROCK1/F-actin/mitochondrial fission pathways.Yap-Hippo 通路通过抑制 ROCK1/F-actin/线粒体分裂通路调节神经母细胞瘤 N2a 细胞的脑缺氧再复氧损伤。
Acta Neurol Belg. 2020 Aug;120(4):879-892. doi: 10.1007/s13760-018-0944-6. Epub 2018 May 23.
3
2-Methoxyestradiol blocks the RhoA/ROCK1 pathway in human aortic smooth muscle cells.2-甲氧基雌二醇阻断人主动脉平滑肌细胞中的RhoA/ROCK1信号通路。
Am J Physiol Endocrinol Metab. 2015 Dec 15;309(12):E995-1007. doi: 10.1152/ajpendo.00267.2015. Epub 2015 Oct 20.
4
Myofibrillogenesis Regulator-1 in Smooth Muscle Cells Modulates Inflammation Signaling Pathways via Regulating ROCK1 Ubiquitination and Degradation to Impact Aortic Dissection.平滑肌细胞中的肌原纤维生成调节因子-1通过调节ROCK1泛素化和降解来调节炎症信号通路,从而影响主动脉夹层。
J Inflamm Res. 2025 Feb 5;18:1719-1738. doi: 10.2147/JIR.S485163. eCollection 2025.
5
Retinol binding protein 4 promotes the phenotypic transformation of vascular smooth muscle cells under high glucose condition via modulating RhoA/ROCK1 pathway.视黄醇结合蛋白 4 通过调节 RhoA/ROCK1 通路促进高糖条件下血管平滑肌细胞的表型转化。
Transl Res. 2023 Sep;259:13-27. doi: 10.1016/j.trsl.2023.03.004. Epub 2023 Mar 30.
6
Targeting matrix stiffness-induced activation of retinal pigment epithelial cells through the RhoA/YAP pathway ameliorates proliferative vitreoretinopathy.通过 RhoA/YAP 通路靶向基质硬度诱导的视网膜色素上皮细胞激活可改善增生性玻璃体视网膜病变。
Exp Eye Res. 2021 Aug;209:108677. doi: 10.1016/j.exer.2021.108677. Epub 2021 Jun 18.
7
B7-H3 promotes the migration and invasion of colorectal cancer cells via regulating the actin cytoskeleton and RhoA/ROCK1/LIMK1 signaling pathway.B7-H3 通过调控细胞骨架肌动蛋白和 RhoA/ROCK1/LIMK1 信号通路促进结直肠癌细胞的迁移和侵袭。
Tissue Cell. 2024 Oct;90:102518. doi: 10.1016/j.tice.2024.102518. Epub 2024 Aug 10.
8
RhoA/ROCK signaling regulates smooth muscle phenotypic modulation and vascular remodeling via the JNK pathway and vimentin cytoskeleton.RhoA/ROCK 信号通路通过 JNK 通路和波形蛋白细胞骨架调节平滑肌表型调节和血管重塑。
Pharmacol Res. 2018 Jul;133:201-212. doi: 10.1016/j.phrs.2018.05.011. Epub 2018 May 20.
9
RHOA activity in expanding blastocysts is essential to regulate HIPPO-YAP signaling and to maintain the trophectoderm-specific gene expression program in a ROCK/actin filament-independent manner.在扩展囊胚中,RHOA 的活性对于调节 HIPPO-YAP 信号通路以及以 ROCK/肌动蛋白丝非依赖的方式维持滋养层特异性基因表达程序是必不可少的。
Mol Hum Reprod. 2019 Feb 1;25(2):43-60. doi: 10.1093/molehr/gay048.
10
Endostatin attenuates PDGF-BB- or TGF-β1-induced HSCs activation via suppressing RhoA/ROCK1 signal pathways.内皮抑素通过抑制RhoA/ROCK1信号通路减弱血小板衍生生长因子-BB或转化生长因子-β1诱导的肝星状细胞激活。
Drug Des Devel Ther. 2019 Jan 11;13:285-290. doi: 10.2147/DDDT.S191617. eCollection 2019.

引用本文的文献

1
CIDEC/FSP27 exacerbates obesity-related abdominal aortic aneurysm by promoting perivascular adipose tissue inflammation.CIDEC/FSP27 通过促进血管周围脂肪组织炎症加剧肥胖相关的腹主动脉瘤。
Life Metab. 2024 Sep 18;4(1):loae035. doi: 10.1093/lifemeta/loae035. eCollection 2025 Feb.

本文引用的文献

1
Aortic Stress Activates an Adaptive Program in Thoracic Aortic Smooth Muscle Cells That Maintains Aortic Strength and Protects Against Aneurysm and Dissection in Mice.主动脉张力激活了胸主动脉平滑肌细胞中的适应性程序,该程序维持主动脉强度并防止小鼠的动脉瘤和夹层。
Arterioscler Thromb Vasc Biol. 2023 Feb;43(2):234-252. doi: 10.1161/ATVBAHA.122.318135. Epub 2022 Dec 29.
2
Legumain Is an Endogenous Modulator of Integrin αvβ3 Triggering Vascular Degeneration, Dissection, and Rupture.组织蛋白酶 S 是整合素 αvβ3 触发血管退行性变、夹层和破裂的内源性调节剂。
Circulation. 2022 Mar;145(9):659-674. doi: 10.1161/CIRCULATIONAHA.121.056640. Epub 2022 Jan 31.
3
Loss of smooth muscle α-actin effects on mechanosensing and cell-matrix adhesions.
平滑肌α-肌动蛋白缺失对机械感知和细胞-基质黏附的影响。
Exp Biol Med (Maywood). 2020 Feb;245(4):374-384. doi: 10.1177/1535370220903012. Epub 2020 Feb 17.
4
YAP and TAZ regulate cell volume.YAP 和 TAZ 调节细胞体积。
J Cell Biol. 2019 Oct 7;218(10):3472-3488. doi: 10.1083/jcb.201902067. Epub 2019 Sep 3.
5
Membrane cholesterol and substrate stiffness co-ordinate to induce the remodelling of the cytoskeleton and the alteration in the biomechanics of vascular smooth muscle cells.膜胆固醇和基质硬度共同作用诱导血管平滑肌细胞骨架重塑和生物力学改变。
Cardiovasc Res. 2019 Jul 1;115(8):1369-1380. doi: 10.1093/cvr/cvy276.
6
Small GTP-Binding Protein GDP Dissociation Stimulator Prevents Thoracic Aortic Aneurysm Formation and Rupture by Phenotypic Preservation of Aortic Smooth Muscle Cells.小分子 GTP 结合蛋白 GDP 解离刺激因子通过维持主动脉平滑肌细胞表型预防胸主动脉瘤的形成和破裂。
Circulation. 2018 Nov 20;138(21):2413-2433. doi: 10.1161/CIRCULATIONAHA.118.035648.
7
Disruption of mechanical stress in extracellular matrix is related to Stanford type A aortic dissection through down-regulation of Yes-associated protein.细胞外基质中机械应力的破坏通过Yes相关蛋白的下调与A型主动脉夹层相关。
Aging (Albany NY). 2016 Sep 5;8(9):1923-1939. doi: 10.18632/aging.101033.
8
Structure of the Elastin-Contractile Units in the Thoracic Aorta and How Genes That Cause Thoracic Aortic Aneurysms and Dissections Disrupt This Structure.胸主动脉中弹性蛋白收缩单元的结构以及导致胸主动脉瘤和夹层的基因如何破坏这种结构。
Can J Cardiol. 2016 Jan;32(1):26-34. doi: 10.1016/j.cjca.2015.11.004. Epub 2015 Nov 10.
9
2015 ATVB Plenary Lecture: translational research on rho-kinase in cardiovascular medicine.2015 ATVB 全会演讲:心血管医学中 Rho 激酶的转化研究。
Arterioscler Thromb Vasc Biol. 2015 Aug;35(8):1756-69. doi: 10.1161/ATVBAHA.115.305353. Epub 2015 Jun 11.
10
Augmented vascular smooth muscle cell stiffness and adhesion when hypertension is superimposed on aging.高血压叠加在衰老之上时,血管平滑肌细胞硬度和黏附性增加。
Hypertension. 2015 Feb;65(2):370-7. doi: 10.1161/HYPERTENSIONAHA.114.04456. Epub 2014 Dec 1.