Actinomycin D-induced apoptosis involves the potassium channel Kv1.3

被引:65
作者
Bock, J
Szabó, I
Jekle, A
Gulbins, E
机构
[1] St Jude Childrens Res Hosp, Dept Immunol, Memphis, TN 38105 USA
[2] Univ Essen Gesamthsch, Dept Mol Biol, D-45122 Essen, Germany
[3] Univ Tubingen, Dept Physiol, D-72076 Tubingen, Germany
[4] CNR, Unit Biomembranes, Padua, Italy
[5] Univ Padua, Dept Biol, Dept Biomed Sci, Padua, Italy
关键词
apoptosis; Kv1.3; cytotoxic agents; actinomycin D;
D O I
10.1016/S0006-291X(02)00695-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Several cytostatic agents are known to induce apoptosis in T-leukemic cells. Although a variety of studies show the central role of apoptosis in cytostatic drug-induced cell death, many molecular details require definition. Here, we demonstrate that cells genetically deficient for the potassium channel Kv1.3 are resistant to apoptosis initiated by the cytostatic drug actinomycin D. Retransfection of Kv1.3 restores sensitivity of the cells to actinomycin D. Cells lacking Kv1.3 fail to respond to actinomycin D with DNA fragmentation, release of cytochrome c, and loss of mitochondrial membrane potential (DeltaPsi(m)). while cells functionally expressing Kv1.3 rapidly undergo those changes indicative for apoptosis. The data indicate a central role of the ion channel Kv1.3 in actinomycin D-triggered apoptosis. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:526 / 531
页数:6
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