[Effects of ROCK-siRNA transfection on Ang II-induced endothelial cell senescence and endothelial microparticles].

细胞与分子免疫学杂志 Pub Date : 2025-09-01
Kai Wang, Yan Wang, Tianqi Chen, Fang Peng, Hui Zhou, Qin Shi
{"title":"[Effects of ROCK-siRNA transfection on Ang II-induced endothelial cell senescence and endothelial microparticles].","authors":"Kai Wang, Yan Wang, Tianqi Chen, Fang Peng, Hui Zhou, Qin Shi","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Objective To investigate the effects of ROCK-siRNA transfection on endothelial cell senescence and endothelial microparticles (EMPs) induced by angiotensin II (Ang II). Methods Human umbilical vein endothelial cells (HUVECs) were treated with Ang II (1.0 μmo/L) to induce cellular senescence models, followed by transfection with ROCK-siRNA. The cells were divided into four groups: control group, model group, negative transfection control group (Ang II combined with NC-siRNA), and ROCK-siRNA transfection group (Ang II combined with ROCK-siRNA). Cellular senescence was assessed by SA-β-Gal staining. EMP levels in cell supernatants and intracellular reactive oxygen species (ROS) levels were assessed using flow cytometry. The expression levels of silenced information regulator 1(SIRT1) and p53 protein in each group were analyzed by Western blotting. Results Following ROCK-siRNA transfection, the number of senescent cells induced by Ang II was significantly reduced, accompanied by decreased CD31<sup>+</sup> EMP levels and suppressed intracellular ROS levels. Meanwhile, the expression levels of SIRT1 were up-regulated, while the expression levels of p53 were down-regulated. Conclusion Silencing ROCK expression suppresses EMP release, reduces ROS generation, regulates the expression of SIRT1 and p53, and ultimately attenuates Ang II-induced endothelial cell senescence.</p>","PeriodicalId":61378,"journal":{"name":"细胞与分子免疫学杂志","volume":"41 9","pages":"778-783"},"PeriodicalIF":0.0000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"细胞与分子免疫学杂志","FirstCategoryId":"3","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Objective To investigate the effects of ROCK-siRNA transfection on endothelial cell senescence and endothelial microparticles (EMPs) induced by angiotensin II (Ang II). Methods Human umbilical vein endothelial cells (HUVECs) were treated with Ang II (1.0 μmo/L) to induce cellular senescence models, followed by transfection with ROCK-siRNA. The cells were divided into four groups: control group, model group, negative transfection control group (Ang II combined with NC-siRNA), and ROCK-siRNA transfection group (Ang II combined with ROCK-siRNA). Cellular senescence was assessed by SA-β-Gal staining. EMP levels in cell supernatants and intracellular reactive oxygen species (ROS) levels were assessed using flow cytometry. The expression levels of silenced information regulator 1(SIRT1) and p53 protein in each group were analyzed by Western blotting. Results Following ROCK-siRNA transfection, the number of senescent cells induced by Ang II was significantly reduced, accompanied by decreased CD31+ EMP levels and suppressed intracellular ROS levels. Meanwhile, the expression levels of SIRT1 were up-regulated, while the expression levels of p53 were down-regulated. Conclusion Silencing ROCK expression suppresses EMP release, reduces ROS generation, regulates the expression of SIRT1 and p53, and ultimately attenuates Ang II-induced endothelial cell senescence.

[ROCK-siRNA转染对angii诱导的内皮细胞衰老和内皮微粒的影响]。
目的探讨转染ROCK-siRNA对血管紧张素II (Ang II)诱导的内皮细胞衰老和内皮微粒(EMPs)的影响。方法用1.0 μmo/L浓度的Ang诱导人脐静脉内皮细胞(HUVECs)衰老,并转染ROCK-siRNA。将细胞分为4组:对照组、模型组、阴性转染对照组(Ang II联合NC-siRNA)、ROCK-siRNA转染组(Ang II联合ROCK-siRNA)。采用SA-β-Gal染色法观察细胞衰老情况。流式细胞术检测细胞上清液中的EMP水平和细胞内活性氧(ROS)水平。Western blotting分析各组沉默信息调节因子1(SIRT1)和p53蛋白的表达水平。结果转染ROCK-siRNA后,Angⅱ诱导的衰老细胞数量明显减少,CD31+ EMP水平下降,细胞内ROS水平受到抑制。同时SIRT1表达水平上调,p53表达水平下调。结论沉默ROCK表达可抑制EMP的释放,减少ROS的产生,调节SIRT1和p53的表达,最终减轻angii诱导的内皮细胞衰老。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
9567
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信