慢病毒介导的Agitoxin表达对细胞内Kv1.3钾通道的选择性抑制

J. Yang, Takeshi Suzuki, Maya Mikami
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引用次数: 0

摘要

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