• 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

过氧化氢诱导的心肌细胞凋亡过程中的心肌细胞基因表达谱分析。

Cardiac myocyte gene expression profiling during H2O2-induced apoptosis.

作者信息

Clerk Angela, Kemp Timothy J, Zoumpoulidou Georgia, Sugden Peter H

机构信息

National Heart and Lung Institute Division, Faculty of Medicine, Imperial College London, London, United Kingdom.

出版信息

Physiol Genomics. 2007 Apr 24;29(2):118-27. doi: 10.1152/physiolgenomics.00168.2006. Epub 2006 Dec 5.

DOI:10.1152/physiolgenomics.00168.2006
PMID:17148688
Abstract

High levels of oxidative stress promote cardiac myocyte death, though lower levels are potentially cytoprotective/anabolic. We examined the changes in gene expression in rat neonatal cardiac myocytes exposed to apoptotic (0.2 mM) or nontoxic (0.04 mM) concentrations of H2O2 (2, 4, or 24 h) using Affymetrix microarrays. Using U34B arrays, we identified a ubiquitously expressed, novel H2O2-responsive gene [putative peroxide-inducible transcript 1 (Perit1)], which generates two alternatively spliced transcripts. Using 230 2.0 arrays, H2O2 (0.04 mM) promoted significant changes in expression of only 32 genes, all of which were seen with 0.2 mM H2O2. We failed to detect any increase in the rate of protein synthesis in cardiac myocytes exposed to <0.1 mM H2O2, further suggesting that global, low concentrations of H2O2 are not anabolic in this system. H2O2 (0.2 mM) promoted significant (P < 0.05, >1.75-fold) changes in expression of 649 mRNAs and 187 RNAs corresponding to no established gene. Of the mRNAs, 114 encoded transcriptional regulators including Krüppel-like factors (Klfs). Quantitative PCR independently verified the changes in Klf expression. Thus, H2O2-induced cardiac myocyte apoptosis is associated with dynamic changes in gene expression. The expression of these genes and their protein products potentially influences the progression of the apoptotic response.

摘要

高水平的氧化应激会促进心肌细胞死亡,不过较低水平的氧化应激可能具有细胞保护/合成代谢作用。我们使用Affymetrix微阵列检测了暴露于凋亡浓度(0.2 mM)或无毒浓度(0.04 mM)的H2O2(处理2、4或24小时)的大鼠新生心肌细胞中基因表达的变化。使用U34B阵列,我们鉴定出一个普遍表达的新型H2O2反应基因[假定的过氧化物诱导转录本1(Perit1)],它产生两种可变剪接转录本。使用230 2.0阵列,H2O2(0.04 mM)仅使32个基因的表达发生显著变化,而这些基因在0.2 mM H2O2处理时也都出现了变化。我们未检测到暴露于<0.1 mM H2O2的心肌细胞中蛋白质合成速率有任何增加,这进一步表明在此系统中,低浓度的H2O2总体上并无合成代谢作用。H2O2(0.2 mM)使649个mRNA和187个对应未确定基因的RNA的表达发生显著(P < 0.05,>1.75倍)变化。在这些mRNA中,有114个编码转录调节因子,包括Krüppel样因子(Klfs)。定量PCR独立验证了Klf表达的变化。因此,H2O2诱导的心肌细胞凋亡与基因表达的动态变化相关。这些基因及其蛋白质产物的表达可能影响凋亡反应的进程。

相似文献

1
Cardiac myocyte gene expression profiling during H2O2-induced apoptosis.过氧化氢诱导的心肌细胞凋亡过程中的心肌细胞基因表达谱分析。
Physiol Genomics. 2007 Apr 24;29(2):118-27. doi: 10.1152/physiolgenomics.00168.2006. Epub 2006 Dec 5.
2
Differential regulation of Krüppel-like factor family transcription factor expression in neonatal rat cardiac myocytes: effects of endothelin-1, oxidative stress and cytokines.新生大鼠心肌细胞中Krüppel样因子家族转录因子表达的差异调节:内皮素-1、氧化应激和细胞因子的作用
Biochim Biophys Acta. 2008 Jun;1783(6):1229-36. doi: 10.1016/j.bbamcr.2008.03.007. Epub 2008 Mar 25.
3
MicroRNA-150 aggravates H2O2-induced cardiac myocyte injury by down-regulating c-myb gene.MicroRNA-150 通过下调 c-myb 基因加重 H2O2 诱导的心肌细胞损伤。
Acta Biochim Biophys Sin (Shanghai). 2013 Sep;45(9):734-41. doi: 10.1093/abbs/gmt067. Epub 2013 Jul 3.
4
Regulation of Bcl-xL expression by H2O2 in cardiac myocytes.过氧化氢对心肌细胞中Bcl-xL表达的调控
J Biol Chem. 2003 Jul 11;278(28):25542-7. doi: 10.1074/jbc.M303760200. Epub 2003 Apr 29.
5
MicroRNA-214 protects cardiac myocytes against H2O2-induced injury.微小RNA-214保护心肌细胞免受过氧化氢诱导的损伤。
J Cell Biochem. 2014 Jan;115(1):93-101. doi: 10.1002/jcb.24636.
6
Differential Gene Expression Patterns in Chicken Cardiomyocytes during Hydrogen Peroxide-Induced Apoptosis.过氧化氢诱导鸡心肌细胞凋亡过程中的差异基因表达模式
PLoS One. 2016 Jan 25;11(1):e0147950. doi: 10.1371/journal.pone.0147950. eCollection 2016.
7
An integrated approach to identify critical transcription factors in the protection against hydrogen peroxide-induced oxidative stress by Danhong injection.丹红注射液通过综合方法鉴定对过氧化氢诱导的氧化应激保护作用中的关键转录因子。
Free Radic Biol Med. 2017 Nov;112:480-493. doi: 10.1016/j.freeradbiomed.2017.07.002. Epub 2017 Aug 16.
8
Cardioprotective stress response in the human fetal heart.人类胎儿心脏中的心脏保护应激反应。
J Thorac Cardiovasc Surg. 2005 May;129(5):1128-36. doi: 10.1016/j.jtcvs.2004.11.055.
9
Urotensin II Protects Cardiomyocytes from Apoptosis Induced by Oxidative Stress through the CSE/H2S Pathway.尾加压素II通过CSE/H2S途径保护心肌细胞免受氧化应激诱导的凋亡。
Int J Mol Sci. 2015 Jun 3;16(6):12482-98. doi: 10.3390/ijms160612482.
10
Catalpol inhibits apoptosis in hydrogen peroxide-induced cardiac myocytes through a mitochondrial-dependent caspase pathway.梓醇通过线粒体依赖的半胱天冬酶途径抑制过氧化氢诱导的心肌细胞凋亡。
Biosci Rep. 2016 Jun 30;36(3). doi: 10.1042/BSR20160132. Print 2016 Jul.

引用本文的文献

1
Emerging multisystem biomarkers in hereditary transthyretin amyloidosis: a pilot study.遗传性转甲状腺素蛋白淀粉样变性症中的新兴多系统生物标志物:一项初步研究。
Sci Rep. 2024 Aug 7;14(1):18281. doi: 10.1038/s41598-024-69123-x.
2
[Different levels and clinical significance of growth differentiation factor-15 in patients with atrial fibrillation].[心房颤动患者中生长分化因子-15的不同水平及其临床意义]
Beijing Da Xue Xue Bao Yi Xue Ban. 2024 Aug 18;56(4):715-721. doi: 10.19723/j.issn.1671-167X.2024.04.027.
3
Myocardial infarction from a tissue engineering and regenerative medicine point of view: A comprehensive review on models and treatments.
从组织工程与再生医学角度看心肌梗死:关于模型与治疗的全面综述
Biophys Rev (Melville). 2022 Sep;3(3):031305. doi: 10.1063/5.0093399. Epub 2022 Aug 30.
4
miRNA-576 Alleviates the Malignant Progression of Atherosclerosis through Downregulating KLF5.miRNA-576 通过下调 KLF5 缓解动脉粥样硬化的恶性进展。
Dis Markers. 2021 Dec 8;2021:5450685. doi: 10.1155/2021/5450685. eCollection 2021.
5
Biomarkers for Heart Failure Prognosis: Proteins, Genetic Scores and Non-coding RNAs.心力衰竭预后的生物标志物:蛋白质、基因评分和非编码RNA。
Front Cardiovasc Med. 2020 Nov 23;7:601364. doi: 10.3389/fcvm.2020.601364. eCollection 2020.
6
The cardiomyocyte "redox rheostat": Redox signalling via the AMPK-mTOR axis and regulation of gene and protein expression balancing survival and death.心肌细胞“氧化还原变阻器”:通过 AMPK-mTOR 轴的氧化还原信号传递以及调节基因和蛋白质表达来平衡存活和死亡。
J Mol Cell Cardiol. 2019 Apr;129:118-129. doi: 10.1016/j.yjmcc.2019.02.006. Epub 2019 Feb 13.
7
protects cardiomyocytes from hypoxia/reoxygenation-induced apoptosis via PTEN/PI3K/p-Akt pathway.通过 PTEN/PI3K/p-Akt 通路保护心肌细胞免受低氧/复氧诱导的凋亡。
Biosci Rep. 2017 Dec 5;37(6). doi: 10.1042/BSR20170899. Print 2017 Dec 22.
8
Growth Differentiation Factor 15 May Predict Mortality of Peripheral and Coronary Artery Diseases and Correlate with Their Risk Factors.生长分化因子 15 可能预测外周动脉疾病和冠状动脉疾病的死亡率,并与这些疾病的危险因素相关。
Mediators Inflamm. 2017;2017:9398401. doi: 10.1155/2017/9398401. Epub 2017 Jul 17.
9
Transcriptome profiling of 3D co-cultured cardiomyocytes and endothelial cells under oxidative stress using a photocrosslinkable hydrogel system.使用可光交联水凝胶系统对氧化应激下的3D共培养心肌细胞和内皮细胞进行转录组分析。
Acta Biomater. 2017 Aug;58:337-348. doi: 10.1016/j.actbio.2017.06.031. Epub 2017 Jun 23.
10
Enrichment of in vivo transcription data from dietary intervention studies with in vitro data provides improved insight into gene regulation mechanisms in the intestinal mucosa.将饮食干预研究中的体内转录数据与体外数据相结合,能够更深入地了解肠道黏膜中的基因调控机制。
Genes Nutr. 2017 Apr 13;12:11. doi: 10.1186/s12263-017-0559-1. eCollection 2017.