Overexpression of the human manganese superoxide dismutase (MnSOD) transgene in subclones of murine hematopoietic progenitor cell line 32D cl 3 decreases irradiation-induced apoptosis but does not alter G2/M or G1/S phase cell cycle arrest.

M W Epperly, J A Bray, P Esocobar, W L Bigbee, S Watkins, J S Greenberger
{"title":"Overexpression of the human manganese superoxide dismutase (MnSOD) transgene in subclones of murine hematopoietic progenitor cell line 32D cl 3 decreases irradiation-induced apoptosis but does not alter G2/M or G1/S phase cell cycle arrest.","authors":"M W Epperly,&nbsp;J A Bray,&nbsp;P Esocobar,&nbsp;W L Bigbee,&nbsp;S Watkins,&nbsp;J S Greenberger","doi":"10.1002/(SICI)1520-6823(1999)7:6<331::AID-ROI3>3.0.CO;2-M","DOIUrl":null,"url":null,"abstract":"To determine whether overexpression of the human MnSOD transgene protected 32D cl 3 hematopoietic progenitor cells from ionizing irradiation, 32D cl 3 cells were co-electroporated with the pRK5 plasmid containing the human MnSOD transgene and SV2-neo plasmid with G418-resistant colonies selected. Two clones (1F2 and 2C6) were identified to overexpress the human MnSOD transgene by nested reverse transcriptase-polymerase chain reaction (RT-PCR) and increased biochemical activity. Measurement of irradiation-induced damage was determined in cells removed from G418 for 1 week before irradiation. Irradiation survival curves, apoptosis tunnel assay, and Comet assay was performed. Cell cycle distribution was determined for each line at 0, 1, 3, 6, 24, and 48 hr after 500 cGy by fixing the cells in 70% ethanol, staining with propidium iodide, and analysis by flow cytometer. Biochemical MnSOD activity in U/mg protein was 2.6 for 32D cl 3 and significantly elevated to 8.4 and 6.6 (P < 0.001) U/mg protein for subclones 1F2 and 2C6, respectively. Irradiation survival curves demonstrated an increased shoulder on the irradiation survival curve for 1F2 and 2C6 cells with an n of 4.95 +/- 0.48 (P = 0.042) and 4.95 +/- 0.13 (P = 0.011), compared with 2.77 +/- 0.20 for 32D cl 3. A higher percent of 32D cl 3 cells demonstrated apoptosis at 24 and 48 hr after 1,000 cGy irradiation, compared with 1F2 and 2C6 cells (at 24 hr, 29.37% +/- 2.01% of 32D cl 3 cells were apoptotic compared with 5.21 +/- 2.61 (P = 0.018) and 5.27 +/- 2.58 (P = 0.004) for 1F2 and 2C6, respectively). Significantly more DNA strand breaks were detected by Comet assay in 32D cl 3 cells (Comet length at 600 cGy of 103.4 +/- 50.3 units, compared with 69.7 +/- 36.3 (P < 0.001) and 48.9 +/- 27.5 (P < 0.001) for 1F2 and 2C6, respectively). In contrast, irradiation-induced cell cycle arrest was similar between the cell lines with a G2/M phase arrest at 6 hr and a G1/S phase arrest at 24 and 48 hr after irradiation. While overexpression of MnSOD increases the shoulder on the irradiation survival curve of 32D cl 3 cells, decreases irradiation-induced apoptosis, and DNA strand breaks by Comet assay, irradiation-induced alterations in cell cycle distribution were not significantly altered. These 32D cl 3 subclonal lines overexpressing MnSOD provide a potentially valuable system with which to study the mechanism of irradiation-induced cell cycle arrest separate from irradiation-induced apoptosis.","PeriodicalId":20894,"journal":{"name":"Radiation oncology investigations","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"1999-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/(SICI)1520-6823(1999)7:6<331::AID-ROI3>3.0.CO;2-M","citationCount":"46","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Radiation oncology investigations","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/(SICI)1520-6823(1999)7:6<331::AID-ROI3>3.0.CO;2-M","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 46

Abstract

To determine whether overexpression of the human MnSOD transgene protected 32D cl 3 hematopoietic progenitor cells from ionizing irradiation, 32D cl 3 cells were co-electroporated with the pRK5 plasmid containing the human MnSOD transgene and SV2-neo plasmid with G418-resistant colonies selected. Two clones (1F2 and 2C6) were identified to overexpress the human MnSOD transgene by nested reverse transcriptase-polymerase chain reaction (RT-PCR) and increased biochemical activity. Measurement of irradiation-induced damage was determined in cells removed from G418 for 1 week before irradiation. Irradiation survival curves, apoptosis tunnel assay, and Comet assay was performed. Cell cycle distribution was determined for each line at 0, 1, 3, 6, 24, and 48 hr after 500 cGy by fixing the cells in 70% ethanol, staining with propidium iodide, and analysis by flow cytometer. Biochemical MnSOD activity in U/mg protein was 2.6 for 32D cl 3 and significantly elevated to 8.4 and 6.6 (P < 0.001) U/mg protein for subclones 1F2 and 2C6, respectively. Irradiation survival curves demonstrated an increased shoulder on the irradiation survival curve for 1F2 and 2C6 cells with an n of 4.95 +/- 0.48 (P = 0.042) and 4.95 +/- 0.13 (P = 0.011), compared with 2.77 +/- 0.20 for 32D cl 3. A higher percent of 32D cl 3 cells demonstrated apoptosis at 24 and 48 hr after 1,000 cGy irradiation, compared with 1F2 and 2C6 cells (at 24 hr, 29.37% +/- 2.01% of 32D cl 3 cells were apoptotic compared with 5.21 +/- 2.61 (P = 0.018) and 5.27 +/- 2.58 (P = 0.004) for 1F2 and 2C6, respectively). Significantly more DNA strand breaks were detected by Comet assay in 32D cl 3 cells (Comet length at 600 cGy of 103.4 +/- 50.3 units, compared with 69.7 +/- 36.3 (P < 0.001) and 48.9 +/- 27.5 (P < 0.001) for 1F2 and 2C6, respectively). In contrast, irradiation-induced cell cycle arrest was similar between the cell lines with a G2/M phase arrest at 6 hr and a G1/S phase arrest at 24 and 48 hr after irradiation. While overexpression of MnSOD increases the shoulder on the irradiation survival curve of 32D cl 3 cells, decreases irradiation-induced apoptosis, and DNA strand breaks by Comet assay, irradiation-induced alterations in cell cycle distribution were not significantly altered. These 32D cl 3 subclonal lines overexpressing MnSOD provide a potentially valuable system with which to study the mechanism of irradiation-induced cell cycle arrest separate from irradiation-induced apoptosis.
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
人锰超氧化物歧化酶(MnSOD)基因在小鼠造血祖细胞系32dcl3亚克隆中的过表达可减少辐照诱导的细胞凋亡,但不改变G2/M或G1/S期细胞周期阻滞。
为了确定过表达人MnSOD转基因是否能保护32D cl 3造血祖细胞免受电离照射,我们将32D cl 3细胞与含有人MnSOD转基因的pRK5质粒和SV2-neo质粒共电穿孔,并选择抗g418菌落。通过巢式逆转录聚合酶链反应(RT-PCR)鉴定出2个克隆(1F2和2C6)过表达人MnSOD基因,生化活性升高。在辐照前1周,对从G418中取出的细胞进行辐照诱导损伤测量。进行辐照存活曲线、细胞凋亡隧道实验和Comet实验。在500 cGy后0、1、3、6、24和48小时,通过70%乙醇固定细胞,碘化丙啶染色,流式细胞仪分析细胞周期分布。32dcl3的生化MnSOD活性为2.6,1F2和2C6亚克隆分别显著提高到8.4和6.6 (P < 0.001) U/mg蛋白。照射生存曲线显示1F2和2C6细胞在照射生存曲线上的n值增加,分别为4.95 +/- 0.48 (P = 0.042)和4.95 +/- 0.13 (P = 0.011),而32D cl 3的n值为2.77 +/- 0.20。与1F2和2C6细胞相比,32D cl 3细胞在1000 cGy照射后24和48小时凋亡的比例更高(24小时时,32D cl 3细胞凋亡的比例为29.37% +/- 2.01%,而1F2和2C6细胞分别为5.21 +/- 2.61 (P = 0.018)和5.27 +/- 2.58 (P = 0.004))。在32D cl3细胞中,Comet检测到更多的DNA链断裂(600 cGy时,彗星长度为103.4 +/- 50.3单位,而1F2和2C6分别为69.7 +/- 36.3 (P < 0.001)和48.9 +/- 27.5 (P < 0.001))。相比之下,辐照诱导的细胞周期阻滞在细胞系之间相似,在照射后6小时出现G2/M期阻滞,在照射后24和48小时出现G1/S期阻滞。虽然MnSOD过表达增加了32D cl3细胞辐照存活曲线上的肩线,减少了辐照诱导的凋亡,并通过Comet实验发现DNA链断裂,但辐照诱导的细胞周期分布的改变没有明显改变。这些过表达MnSOD的32D cl3亚克隆系为研究辐照诱导的细胞周期阻滞与辐照诱导的细胞凋亡的机制提供了一个潜在的有价值的系统。
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
自引率
0.00%
发文量
0
期刊最新文献
Molecular and anatomic considerations in the pathogenesis of breast cancer. Telomeric length in individuals and cell lines with altered p53 status. Effect of combined adoptive immunotherapy and radiotherapy on tumor growth. PSA kinetics following I-125 radioactive seed implantation in the treatment of T1-T2 prostate cancer. Hyperfractionated and accelerated-hyperfractionated radiotherapy for glioblastoma multiforme.
×
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