二甲苯磺酸乙烯酯对永生化莱德细胞系R2C和MA-10与内分泌功能有关的基因启动子活性的影响

IF 2.9 Q2 TOXICOLOGY Current Research in Toxicology Pub Date : 2024-01-01 DOI:10.1016/j.crtox.2023.100147
Jorge W.F. de Barros , Kenley Joule Pierre , Wilma De G. Kempinas , Jacques J. Tremblay
{"title":"二甲苯磺酸乙烯酯对永生化莱德细胞系R2C和MA-10与内分泌功能有关的基因启动子活性的影响","authors":"Jorge W.F. de Barros ,&nbsp;Kenley Joule Pierre ,&nbsp;Wilma De G. Kempinas ,&nbsp;Jacques J. Tremblay","doi":"10.1016/j.crtox.2023.100147","DOIUrl":null,"url":null,"abstract":"<div><p>Ethylene dimethanesulfonate (EDS) is a molecule with known selective cytotoxicity on adult Leydig cells. A single intraperitoneal injection in rats but not mice, leads to male androgen deprivation and infertility. <em>In vitro</em> studies using rat and mouse immortalized Leydig cell lines, showed similar effects of cell death promoted by EDS in rat cells as seen <em>in vivo</em>, and suggest that EDS affects gene transcription, which could firstly compromise steroidogenesis before the apoptosis process. Using gene reporter assay, this study aimed to investigate EDS effects on the promoter activity of genes important for endocrine function (<em>Star</em>, <em>Insl3</em>) and response to toxic agents (<em>Gsta3</em>) in immortalized Leydig cell lines (rat R2C and mouse MA-10 cells), as well as identify possible EDS-responsive elements in the <em>Star</em> gene promoter. EDS exposure of R2C and MA-10 Leydig cells increased <em>Gsta3</em> promoter activity after 4 h of treatment and decreased <em>Insl3</em> promoter activity only in R2C cells after 24 h of treatment. EDS also decreased <em>Star</em> promoter activity in both Leydig cell lines. Using R2C cells, the EDS-responsive region in the <em>Star</em> promoter was located between −400 and −195 bp. This suggests that this region and the associated transcription factors, which include MEF2, might be targeted by EDS. Additional somatic gonadal cell lines expressing <em>Star</em> were used and EDS did not affect <em>Star</em> promoter activity in DC3 granulosa cells while <em>Star</em> promoter activity was increased in MSC-1 Sertoli cells after 24 h of treatment. This study contributes to the knowledge regarding the mechanism of EDS action in Leydig cells, and in other gonadal cell lineages, and brings new light regarding the rats and mice differential susceptibility to EDS effects, in addition to providing new avenues for experimental approaches to better understand Leydig cell function and dynamics in different rodent species.</p></div>","PeriodicalId":11236,"journal":{"name":"Current Research in Toxicology","volume":null,"pages":null},"PeriodicalIF":2.9000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2666027X23000452/pdfft?md5=7638e3700b61387d77ad30d1e6ae81c8&pid=1-s2.0-S2666027X23000452-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Ethylene dimethanesulfonate effects on gene promoter activities related to the endocrine function of immortalized Leydig cell lines R2C and MA-10\",\"authors\":\"Jorge W.F. de Barros ,&nbsp;Kenley Joule Pierre ,&nbsp;Wilma De G. Kempinas ,&nbsp;Jacques J. Tremblay\",\"doi\":\"10.1016/j.crtox.2023.100147\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Ethylene dimethanesulfonate (EDS) is a molecule with known selective cytotoxicity on adult Leydig cells. A single intraperitoneal injection in rats but not mice, leads to male androgen deprivation and infertility. <em>In vitro</em> studies using rat and mouse immortalized Leydig cell lines, showed similar effects of cell death promoted by EDS in rat cells as seen <em>in vivo</em>, and suggest that EDS affects gene transcription, which could firstly compromise steroidogenesis before the apoptosis process. Using gene reporter assay, this study aimed to investigate EDS effects on the promoter activity of genes important for endocrine function (<em>Star</em>, <em>Insl3</em>) and response to toxic agents (<em>Gsta3</em>) in immortalized Leydig cell lines (rat R2C and mouse MA-10 cells), as well as identify possible EDS-responsive elements in the <em>Star</em> gene promoter. EDS exposure of R2C and MA-10 Leydig cells increased <em>Gsta3</em> promoter activity after 4 h of treatment and decreased <em>Insl3</em> promoter activity only in R2C cells after 24 h of treatment. EDS also decreased <em>Star</em> promoter activity in both Leydig cell lines. Using R2C cells, the EDS-responsive region in the <em>Star</em> promoter was located between −400 and −195 bp. This suggests that this region and the associated transcription factors, which include MEF2, might be targeted by EDS. Additional somatic gonadal cell lines expressing <em>Star</em> were used and EDS did not affect <em>Star</em> promoter activity in DC3 granulosa cells while <em>Star</em> promoter activity was increased in MSC-1 Sertoli cells after 24 h of treatment. This study contributes to the knowledge regarding the mechanism of EDS action in Leydig cells, and in other gonadal cell lineages, and brings new light regarding the rats and mice differential susceptibility to EDS effects, in addition to providing new avenues for experimental approaches to better understand Leydig cell function and dynamics in different rodent species.</p></div>\",\"PeriodicalId\":11236,\"journal\":{\"name\":\"Current Research in Toxicology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.9000,\"publicationDate\":\"2024-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2666027X23000452/pdfft?md5=7638e3700b61387d77ad30d1e6ae81c8&pid=1-s2.0-S2666027X23000452-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current Research in Toxicology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2666027X23000452\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"TOXICOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Research in Toxicology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666027X23000452","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"TOXICOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

二甲苯磺酸乙烯酯(EDS)是一种已知对成年髓质细胞具有选择性细胞毒性的分子。大鼠腹腔注射一次就会导致雄性雄性激素缺乏和不育,小鼠则不会。使用大鼠和小鼠永生化 Leydig 细胞系进行的体外研究显示,EDS 在大鼠细胞中促进细胞死亡的效果与在体内看到的相似,并表明 EDS 会影响基因转录,这可能会在细胞凋亡过程之前首先影响类固醇的生成。本研究采用基因报告分析法,旨在研究EDS对永生化Leydig细胞系(大鼠R2C和小鼠MA-10细胞)中对内分泌功能(Star、Insl3)和对毒物反应(Gsta3)有重要影响的基因启动子活性的影响,并确定Star基因启动子中可能存在的EDS反应元件。R2C和MA-10 Leydig细胞暴露于EDS后,Gsta3启动子活性在处理4小时后增加,而Insl3启动子活性在处理24小时后仅在R2C细胞中降低。EDS 还降低了两种 Leydig 细胞系中 Star 启动子的活性。利用 R2C 细胞,Star 启动子中的 EDS 反应区位于 -400 和 -195 bp 之间。这表明该区域及相关转录因子(包括 MEF2)可能是 EDS 的靶标。研究人员还使用了其他表达Star的体细胞系,结果表明EDS并不影响DC3颗粒细胞中Star启动子的活性,而MSC-1 Sertoli细胞中Star启动子的活性在处理24小时后有所增加。这项研究有助于了解 EDS 在 Leydig 细胞和其他性腺细胞系中的作用机制,并为大鼠和小鼠对 EDS 影响的不同易感性带来了新的启示,此外还为实验方法提供了新的途径,以更好地了解不同啮齿动物物种中 Leydig 细胞的功能和动态。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

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
Ethylene dimethanesulfonate effects on gene promoter activities related to the endocrine function of immortalized Leydig cell lines R2C and MA-10

Ethylene dimethanesulfonate (EDS) is a molecule with known selective cytotoxicity on adult Leydig cells. A single intraperitoneal injection in rats but not mice, leads to male androgen deprivation and infertility. In vitro studies using rat and mouse immortalized Leydig cell lines, showed similar effects of cell death promoted by EDS in rat cells as seen in vivo, and suggest that EDS affects gene transcription, which could firstly compromise steroidogenesis before the apoptosis process. Using gene reporter assay, this study aimed to investigate EDS effects on the promoter activity of genes important for endocrine function (Star, Insl3) and response to toxic agents (Gsta3) in immortalized Leydig cell lines (rat R2C and mouse MA-10 cells), as well as identify possible EDS-responsive elements in the Star gene promoter. EDS exposure of R2C and MA-10 Leydig cells increased Gsta3 promoter activity after 4 h of treatment and decreased Insl3 promoter activity only in R2C cells after 24 h of treatment. EDS also decreased Star promoter activity in both Leydig cell lines. Using R2C cells, the EDS-responsive region in the Star promoter was located between −400 and −195 bp. This suggests that this region and the associated transcription factors, which include MEF2, might be targeted by EDS. Additional somatic gonadal cell lines expressing Star were used and EDS did not affect Star promoter activity in DC3 granulosa cells while Star promoter activity was increased in MSC-1 Sertoli cells after 24 h of treatment. This study contributes to the knowledge regarding the mechanism of EDS action in Leydig cells, and in other gonadal cell lineages, and brings new light regarding the rats and mice differential susceptibility to EDS effects, in addition to providing new avenues for experimental approaches to better understand Leydig cell function and dynamics in different rodent species.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Current Research in Toxicology
Current Research in Toxicology Environmental Science-Health, Toxicology and Mutagenesis
CiteScore
4.70
自引率
3.00%
发文量
33
审稿时长
82 days
期刊最新文献
Editorial Board Contents Evaluation of the diphenyl herbicide, oxyfluorfen, for effects on thyroid hormones in the juvenile rat Ethylene dimethanesulfonate effects on gene promoter activities related to the endocrine function of immortalized Leydig cell lines R2C and MA-10 Placental transfer of tofacitinib in the ex vivo dual-side human placenta perfusion model
×
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