EOLA1 Inhibits Lipopolysaccharide-Induced Vascular Cell Adhesion Molecule-1 Expression by Association with MT2A in ECV304 Cells

IF 2.6 Q3 IMMUNOLOGY International Journal of Inflammation Pub Date : 2015-12-31 DOI:10.1155/2015/301562
Weiling Leng, Xiaotian Lei, Hao Meng, Xinshou Ouyang, Z. Liang
{"title":"EOLA1 Inhibits Lipopolysaccharide-Induced Vascular Cell Adhesion Molecule-1 Expression by Association with MT2A in ECV304 Cells","authors":"Weiling Leng, Xiaotian Lei, Hao Meng, Xinshou Ouyang, Z. Liang","doi":"10.1155/2015/301562","DOIUrl":null,"url":null,"abstract":"Our research group firstly discovered endothelial-overexpressed lipopolysaccharide-associated factor 1 (EOLA1, GenBank number AY074889) as a lipopolysaccharide (LPS) responsive gene in ECV304 cells. The previous studies have further demonstrated the association of EOLA1 with metallothionein 2A (MT2A), while the role of EOLA1 during LPS-induced inflammatory response in ECV304 cells is unknown. In this report, we determined the subcellular localization of EOLA1 and the regulatory capacity of EOLA1 on vascular cell adhesion molecule-1 (VCAM-1) in response to LPS in ECV304 cells. Our results show that EOLA1 is broadly diffuse in the cells, and EOLA1 expression is dramatically induced by LPS. EOLA1 knockdown results in significant enhancement of LPS-induced VCAM-1 production. Consistent with this, overexpression of EOLA1 leads to the reduction of LPS-induced VCAM-1 production. Furthermore, MT2A knockdown reduces LPS-induced VCAM-1 production. Collectively, our results demonstrate a negative regulatory role of EOLA1 on LPS-induced VCAM-1 expression involving its association with MT2A in ECV304 cells.","PeriodicalId":14004,"journal":{"name":"International Journal of Inflammation","volume":"14 1","pages":""},"PeriodicalIF":2.6000,"publicationDate":"2015-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"6","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Inflammation","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/2015/301562","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 6

Abstract

Our research group firstly discovered endothelial-overexpressed lipopolysaccharide-associated factor 1 (EOLA1, GenBank number AY074889) as a lipopolysaccharide (LPS) responsive gene in ECV304 cells. The previous studies have further demonstrated the association of EOLA1 with metallothionein 2A (MT2A), while the role of EOLA1 during LPS-induced inflammatory response in ECV304 cells is unknown. In this report, we determined the subcellular localization of EOLA1 and the regulatory capacity of EOLA1 on vascular cell adhesion molecule-1 (VCAM-1) in response to LPS in ECV304 cells. Our results show that EOLA1 is broadly diffuse in the cells, and EOLA1 expression is dramatically induced by LPS. EOLA1 knockdown results in significant enhancement of LPS-induced VCAM-1 production. Consistent with this, overexpression of EOLA1 leads to the reduction of LPS-induced VCAM-1 production. Furthermore, MT2A knockdown reduces LPS-induced VCAM-1 production. Collectively, our results demonstrate a negative regulatory role of EOLA1 on LPS-induced VCAM-1 expression involving its association with MT2A in ECV304 cells.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
EOLA1通过与MT2A联合抑制ECV304细胞中脂多糖诱导的血管细胞粘附分子-1的表达
本课题组首次在ECV304细胞中发现内皮过表达的脂多糖相关因子1 (EOLA1, GenBank编号AY074889)作为脂多糖(LPS)应答基因。先前的研究进一步证实了EOLA1与金属硫蛋白2A (metallothionein 2A, MT2A)的关联,而EOLA1在lps诱导的ECV304细胞炎症反应中的作用尚不清楚。在本报告中,我们在ECV304细胞中测定了EOLA1的亚细胞定位以及EOLA1对血管细胞粘附分子-1 (VCAM-1)响应LPS的调节能力。我们的研究结果表明,EOLA1在细胞中广泛弥散,并且LPS显著诱导EOLA1的表达。EOLA1敲低导致lps诱导的VCAM-1产生显著增强。与此一致的是,过表达EOLA1导致lps诱导的VCAM-1产生减少。此外,MT2A敲除可减少lps诱导的VCAM-1产生。总之,我们的研究结果表明EOLA1对lps诱导的ECV304细胞中VCAM-1表达的负调控作用涉及其与MT2A的关联。
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 去求助
来源期刊
CiteScore
3.80
自引率
0.00%
发文量
16
审稿时长
16 weeks
期刊最新文献
Extended Inflammation Parameters (EIP) as Markers of Inflammation in Systemic Sclerosis. The Effect of Endotoxin-Induced Inflammation on the Activity of the Somatotropic Axis in Sheep. Characterization of a New Immunosuppressive and Antimicrobial Peptide, DRS-DA2, Isolated from the Mexican Frog, Pachymedusa dacnicolor. Association of Epstein-Barr Virus (EBV) and Human Endogenous Retroviruses (HERV) with Multiple Sclerosis in Northwest of Iran. Irisin and Cardiometabolic Disorders in Obesity: A Systematic Review.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1