Expression of the selectable marker gene bsrm in BALB/MK cells induces apoptosis by overproduction of hydrogen peroxide

Author:

Takeshita Daniela12345,Bento Fernanda Mara12345,Chammas Roger12345,Belizário José Ernesto12345,Carmona Adriana Karaoglanovic12345,Konno Katsuhiro12345,Lopes de Melo Robson12345,Molina Gustavo12345,Lisboa Bianca Cristina Garcia12345,Han Sang Won12345

Affiliation:

1. Department of Biophysics, UNIFESP, São Paulo-SP, Brazil.

2. Department of Radiology, FM-USP, São Paulo-SP, Brazil.

3. Department of Pharmacology, ICB-USP, São Paulo-SP, Brazil.

4. Butantan Institute, São Paulo-SP, Brazil.

5. Interdisciplinary Center for Gene Therapy, UNIFESP, Rua Mirassol 207, São Paulo-SP, 04044-010, Brazil.

Abstract

Transduction of the retroviral vector LBmSN, which expresses the blasticidin S resistance gene bsrm in the murine keratinocyte cell line BALB/MK, induces death in these cells. Cell death is caused by a factor called DOKEB (death factor obtained from keratinocytes expressing bsrm), which is released before the cells' death. In this report we describe and discuss the purification and characterization of DOKEB. Our results were as follows. (i) The 5-day-old medium from the modified BALB/MK cells with LBmSN was used for purification and characterization by filtration and chromatography: DOKEB was a stable and highly hydrophilic compound, with a molecular mass less than that of 1 amino acid. (ii) The conditioned medium containing DOKEB was reactive against thiobarbituric acid and dichlorofluorescein diacetate. (iii) DOKEB activity was neutralized by the incubation of the conditioned medium with catalase. Therefore, our conclusion is that the BALB/MK cells expressing bsrm produce a large amount of hydrogen peroxide, which catalyzes the process of apoptosis of those cells.

Publisher

Canadian Science Publishing

Subject

Cell Biology,Molecular Biology,Biochemistry

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3