Koszela-Piotrowska Izabela, Choma Katarzyna, Bednarczyk Piotr, Dołowy Krzysztof, Szewczyk Adam, Kunz Wolfram S, Malekova Lubica, Kominkova Viera, Ondrias Karol
Laboratory of Intracellular Ion Channels, Nencki Institute of Experimental Biology, Pasteura 3, 02-093, Warsaw, Poland.
Cell Mol Biol Lett. 2007;12(4):493-508. doi: 10.2478/s11658-007-0019-9. Epub 2007 Apr 25.
Ion channels selective for chloride ions are present in all biological membranes, where they regulate the cell volume or membrane potential. Various chloride channels from mitochondrial membranes have been described in recent years. The aim of our study was to characterize the effect of stilbene derivatives on single-chloride channel activity in the inner mitochondrial membrane. The measurements were performed after the reconstitution into a planar lipid bilayer of the inner mitochondrial membranes from rat skeletal muscle (SMM), rat brain (BM) and heart (HM) mitochondria. After incorporation in a symmetric 450/450 mM KCl solution (cis/trans), the chloride channels were recorded with a mean conductance of 155 +/- 5 pS (rat skeletal muscle) and 120 +/- 16 pS (rat brain). The conductances of the chloride channels from the rat heart mitochondria in 250/50 mM KCl (cis/trans) gradient solutions were within the 70-130 pS range. The chloride channels were inhibited by these two stilbene derivatives: 4,4'-diisothiocyanostilbene-2,2'-disulfonic acid (DIDS) and 4-acetamido-4'-isothiocyanostilbene-2,2'-disulfonic acid (SITS). The skeletal muscle mitochondrial chloride channel was blocked after the addition of 1 mM DIDS or SITS, whereas the brain mitochondrial channel was blocked by 300 microM DIDS or SITS. The chloride channel from the rat heart mitochondria was inhibited by 50-100 microM DIDS. The inhibitory effect of DIDS was irreversible. Our results confirm the presence of chloride channels sensitive to stilbene derivatives in the inner mitochondrial membrane from rat skeletal muscle, brain and heart cells.
对氯离子具有选择性的离子通道存在于所有生物膜中,在这些膜中它们调节细胞体积或膜电位。近年来,已经描述了来自线粒体膜的各种氯离子通道。我们研究的目的是表征芪衍生物对线粒体内膜中单个氯离子通道活性的影响。测量是在将大鼠骨骼肌(SMM)、大鼠脑(BM)和心脏(HM)线粒体的线粒体内膜重构到平面脂质双层后进行的。在掺入对称的450/450 mM KCl溶液(顺式/反式)后,记录到的氯离子通道平均电导为155±5 pS(大鼠骨骼肌)和120±16 pS(大鼠脑)。在250/50 mM KCl(顺式/反式)梯度溶液中,大鼠心脏线粒体氯离子通道的电导在70 - 130 pS范围内。这两种芪衍生物:4,4'-二异硫氰基芪-2,2'-二磺酸(DIDS)和4-乙酰氨基-4'-异硫氰基芪-2,2'-二磺酸(SITS)可抑制氯离子通道。加入1 mM DIDS或SITS后,骨骼肌线粒体氯离子通道被阻断,而脑线粒体通道被300 microM DIDS或SITS阻断。大鼠心脏线粒体的氯离子通道被50 - 100 microM DIDS抑制。DIDS的抑制作用是不可逆的。我们的结果证实了在大鼠骨骼肌、脑和心脏细胞的线粒体内膜中存在对芪衍生物敏感的氯离子通道。