过氧化氢诱导肾细胞系凋亡

Khalil Alhalfawy, Bahgat A. Elfiky, A. Zahran, M. Zayed
{"title":"过氧化氢诱导肾细胞系凋亡","authors":"Khalil Alhalfawy, Bahgat A. Elfiky, A. Zahran, M. Zayed","doi":"10.21608/jbaar.2022.228865","DOIUrl":null,"url":null,"abstract":"Background: Hydrogen peroxide is currently the most widely used as an apoptosis inducer due to its broad cytotoxic efficacy against nearly all cell types. cytotoxicity is achieved over a wide range of doses Objective: To evaluate the cytotoxic effect of hydrogen peroxide on renal cell lines by detecting RIPK1. Methods: In this study, we used a Vero cell line treated with H 2 O 2 at concentrations 0.1 mM, 0.2 mM, 0.4 mM, 0.8 mM, and 1.6 mM and examined after 30 min,1hour,2hours,3hours, 4hours and 5 hours. by using MTT assay to detect cytotoxicity to cell line (by detecting cell viability). Spectrophotometrically measure the absorbance at a wavelength of 570 nm. Measure the background absorbance of multi-well plates at 690 nm and subtract from the 450 nm measurement. Sub-lethal dose to renal cell line is one treated with 1.6 mM for 5 hours. groups group 1: renal cell line as control which not treated by H2O2. group 2: Sub-lethal which renal cell line treated by concentration 1.6 mM of H2O2 for 5 hours. Results: H2O2 is cytotoxic to renal cell line by concentration from 0.1 mM to 1.6 mM. RIPK1 gene expressed in renal cell line treated by H2O2. The sublethal dose reached 1.6 mM for 5 hours. There is a significant difference between the 2 groups by detecting the expression of the RIPK1 gene.","PeriodicalId":15163,"journal":{"name":"Journal of Bioscience and Applied Research","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2022-04-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Induction of renal cell line apoptosis by hydrogen peroxide\",\"authors\":\"Khalil Alhalfawy, Bahgat A. Elfiky, A. Zahran, M. Zayed\",\"doi\":\"10.21608/jbaar.2022.228865\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background: Hydrogen peroxide is currently the most widely used as an apoptosis inducer due to its broad cytotoxic efficacy against nearly all cell types. cytotoxicity is achieved over a wide range of doses Objective: To evaluate the cytotoxic effect of hydrogen peroxide on renal cell lines by detecting RIPK1. Methods: In this study, we used a Vero cell line treated with H 2 O 2 at concentrations 0.1 mM, 0.2 mM, 0.4 mM, 0.8 mM, and 1.6 mM and examined after 30 min,1hour,2hours,3hours, 4hours and 5 hours. by using MTT assay to detect cytotoxicity to cell line (by detecting cell viability). Spectrophotometrically measure the absorbance at a wavelength of 570 nm. Measure the background absorbance of multi-well plates at 690 nm and subtract from the 450 nm measurement. Sub-lethal dose to renal cell line is one treated with 1.6 mM for 5 hours. groups group 1: renal cell line as control which not treated by H2O2. group 2: Sub-lethal which renal cell line treated by concentration 1.6 mM of H2O2 for 5 hours. Results: H2O2 is cytotoxic to renal cell line by concentration from 0.1 mM to 1.6 mM. RIPK1 gene expressed in renal cell line treated by H2O2. The sublethal dose reached 1.6 mM for 5 hours. There is a significant difference between the 2 groups by detecting the expression of the RIPK1 gene.\",\"PeriodicalId\":15163,\"journal\":{\"name\":\"Journal of Bioscience and Applied Research\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-04-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Bioscience and Applied Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.21608/jbaar.2022.228865\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Bioscience and Applied Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21608/jbaar.2022.228865","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

背景:过氧化氢对几乎所有类型的细胞都具有广泛的细胞毒性,是目前应用最广泛的细胞凋亡诱导剂。目的:通过检测RIPK1,评价过氧化氢对肾细胞系的细胞毒性作用。方法:采用浓度分别为0.1 mM、0.2 mM、0.4 mM、0.8 mM、1.6 mM的h2o2处理Vero细胞株,分别于30min、1h、2h、3h、4h、5h后进行检测。采用MTT法检测细胞系的细胞毒性(通过检测细胞活力)。分光光度法测量波长为570nm处的吸光度。在690 nm处测量多孔板的背景吸光度,并从450 nm测量值中减去。对肾细胞系的亚致死剂量为1.6 mM,作用5小时。组1:未经H2O2处理的肾细胞系作为对照。2组:浓度为1.6 mM的H2O2处理肾细胞株5小时后亚致死。结果:H2O2浓度在0.1 mM ~ 1.6 mM范围内对肾细胞株具有细胞毒性。亚致死剂量达1.6 mM,持续5小时。通过检测RIPK1基因的表达,两组间存在显著差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Induction of renal cell line apoptosis by hydrogen peroxide
Background: Hydrogen peroxide is currently the most widely used as an apoptosis inducer due to its broad cytotoxic efficacy against nearly all cell types. cytotoxicity is achieved over a wide range of doses Objective: To evaluate the cytotoxic effect of hydrogen peroxide on renal cell lines by detecting RIPK1. Methods: In this study, we used a Vero cell line treated with H 2 O 2 at concentrations 0.1 mM, 0.2 mM, 0.4 mM, 0.8 mM, and 1.6 mM and examined after 30 min,1hour,2hours,3hours, 4hours and 5 hours. by using MTT assay to detect cytotoxicity to cell line (by detecting cell viability). Spectrophotometrically measure the absorbance at a wavelength of 570 nm. Measure the background absorbance of multi-well plates at 690 nm and subtract from the 450 nm measurement. Sub-lethal dose to renal cell line is one treated with 1.6 mM for 5 hours. groups group 1: renal cell line as control which not treated by H2O2. group 2: Sub-lethal which renal cell line treated by concentration 1.6 mM of H2O2 for 5 hours. Results: H2O2 is cytotoxic to renal cell line by concentration from 0.1 mM to 1.6 mM. RIPK1 gene expressed in renal cell line treated by H2O2. The sublethal dose reached 1.6 mM for 5 hours. There is a significant difference between the 2 groups by detecting the expression of the RIPK1 gene.
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
自引率
0.00%
发文量
0
×
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:481959085
Book学术官方微信