Selective Inhibition of Intracellular Kv1.3 Potassium Channels by Lentivirus-Mediated Expression of Agitoxin

J. Yang, Takeshi Suzuki, Maya Mikami
{"title":"Selective Inhibition of Intracellular Kv1.3 Potassium Channels by Lentivirus-Mediated Expression of Agitoxin","authors":"J. Yang, Takeshi Suzuki, Maya Mikami","doi":"10.26502/jbb.2642-91280012","DOIUrl":null,"url":null,"abstract":"Non-plasma membrane Kv1.3 voltage-gated potassium channels, particularly those localized to the inner mitochondrial membrane, is pro-survival in that inhibition of these channels enhances apoptosis of cancer cells. Paradoxically, cells that lack Kv1.3 show resistance to cytotoxic agents suggesting a pro-death role of the same channels. Currently reported genetic and pharmacological reagents block both plasma membrane and intracellular Kv1.3 and lack absolute selectivity for intracellular Kv1.3. We designed a lentivirus for intracellular expression of the Kv1.3-selective peptide toxin agitoxin and created a Jurkat lymphocyte cell line that constitutively expressed intracellular agitoxin to selectively inhibit intracellular Kv1.3. Agitoxin-expressing Jurkat cells demonstrated relative resistance to cytokine-induced apoptosis, whereas direct extracellular application of agitoxin, or control cells expressing EGFP alone, failed to demonstrate this cyto- protection. We concluded that the intracellular Kv1.3 served a pro-death role, and a selective inhibition of this target reduced lymphocyte apoptosis by cytokine stimulation as reported previously for Kv1.3-null cells.","PeriodicalId":15066,"journal":{"name":"Journal of Biotechnology and Biomedicine","volume":"54 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Biotechnology and Biomedicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.26502/jbb.2642-91280012","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Non-plasma membrane Kv1.3 voltage-gated potassium channels, particularly those localized to the inner mitochondrial membrane, is pro-survival in that inhibition of these channels enhances apoptosis of cancer cells. Paradoxically, cells that lack Kv1.3 show resistance to cytotoxic agents suggesting a pro-death role of the same channels. Currently reported genetic and pharmacological reagents block both plasma membrane and intracellular Kv1.3 and lack absolute selectivity for intracellular Kv1.3. We designed a lentivirus for intracellular expression of the Kv1.3-selective peptide toxin agitoxin and created a Jurkat lymphocyte cell line that constitutively expressed intracellular agitoxin to selectively inhibit intracellular Kv1.3. Agitoxin-expressing Jurkat cells demonstrated relative resistance to cytokine-induced apoptosis, whereas direct extracellular application of agitoxin, or control cells expressing EGFP alone, failed to demonstrate this cyto- protection. We concluded that the intracellular Kv1.3 served a pro-death role, and a selective inhibition of this target reduced lymphocyte apoptosis by cytokine stimulation as reported previously for Kv1.3-null 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
慢病毒介导的Agitoxin表达对细胞内Kv1.3钾通道的选择性抑制
非质膜Kv1.3电压门控钾通道,特别是那些位于线粒体内膜的通道,对这些通道的抑制促进了癌细胞的凋亡,从而促进了癌细胞的存活。矛盾的是,缺乏Kv1.3的细胞表现出对细胞毒性药物的抗性,这表明相同通道具有促死亡作用。目前报道的遗传和药理学试剂可阻断质膜和细胞内Kv1.3,对细胞内Kv1.3缺乏绝对选择性。我们设计了一种慢病毒用于细胞内表达Kv1.3选择性肽毒素agitoxin,并建立了一个Jurkat淋巴细胞系,组成性表达细胞内agitoxin以选择性抑制细胞内Kv1.3。表达agitoxin的Jurkat细胞表现出对细胞因子诱导的凋亡的相对抗性,而直接在细胞外应用agitoxin,或单独表达EGFP的对照细胞,未能表现出这种细胞保护作用。我们得出的结论是,细胞内Kv1.3具有促死亡作用,并且该靶点的选择性抑制通过细胞因子刺激减少了淋巴细胞凋亡,正如之前报道的Kv1.3缺失细胞。
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
The ERK Signaling Cascade Inhibits Gonadotropin-Stimulated Steroidogenesis. Immunomodulatory Effect of Electromagnetic Field in the Treatment of Traumatic Brain Injury. Accelerating Minimap2 for Accurate Long Read Alignment on GPUs. Cellular Mechanisms of Electromagnetic Field in Traumatic Brain Injury. Therapeutic Potential of "Smart" Exosomes in Peripheral Nerve Regeneration.
×
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