首页> 外文期刊>Toxicon: An International Journal Devoted to the Exchange of Knowledge on the Poisons Derived from Animals, Plants and Microorganisms >Ca2+ and Na+ contribute to the swelling of differentiated neuroblastoma cells induced by equinatoxin-II
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Ca2+ and Na+ contribute to the swelling of differentiated neuroblastoma cells induced by equinatoxin-II

机译:Ca2 +和Na +促进由Equinatoxin-II诱导的分化的神经母细胞瘤细胞肿胀

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Equinatoxin-II (EqTx-II), a cytotoxic protein (mol.wt 20 kDa) isolated from the sea anemone Actinia equina, was found to consistently increase the three-dimensional projected area of differentiated neuroblastoma (NG108-15) cells provided Ca2+ was present in the medium. No swelling was detected when external NaCl was replaced by sucrose, but replacement of NaCl by Na-isethionate did not prevent the swelling, as revealed by confocal laser scanning microscopy. In addition, microspectrofluorometric measurements in cells preloaded with the Ca2+ indicator fura-2/AM revealed that EqTx-II (100 nM) markedly increased the fluorescence (F-340/F-380) ratio indicating a rise of intracellular Ca2+ concentration ([Ca2+](i)). The elevation of [Ca2+](i) exhibited two components that seem to be related to the kinetics of EqTx-II-induced Ca2+ entry since pretreatment of cells with Ca2+-ATPase inhibitors (thapsigargin), Ca2+ channel blockers (nifedipine and Gd3+) or prolonged exposure to a high K+ (75 mM) medium did not alter EqTx-II-induced Ca2+ signals. As far as we know, this is the first demonstration that EqTx-II causes swelling of neuroblastoma cells and that this effect is correlated both with an increase of [Ca2+](i) and needs the presence of extracellular Na+. It is suggested that EqTx-II has the ability to insert into the plasma membrane of neuroblastoma cells and to form pores altering the membrane permeability and the intracellular osmolality, inducing a marked influx of water into the cells. (C) 2000 Elsevier Science Ltd. All rights reserved. [References: 27]
机译:从海葵Actinia equina分离出的一种细胞毒性蛋白(分子量20 kDa)EquinT毒素-II(EqTx-II)被发现能够持续增加分化的神经母细胞瘤(NG108-15)细胞的三维投影面积,前提是Ca2 +为存在于媒介中。共焦激光扫描显微镜显示,当用蔗糖代替外部NaCl时,未检测到溶胀,但是用异羟磺酸钠替代NaCl并不能防止溶胀。此外,在预装有Ca2 +指示剂fura-2 / AM的细胞中进行的微光谱荧光测量显示,EqTx-II(100 nM)显着增加了荧光(F-340 / F-380)比率,表明细胞内Ca2 +浓度([Ca2 + ](一世))。 [Ca2 +](i)的升高表现出两个与EqTx-II诱导的Ca2 +进入动力学有关的成分,因为用Ca2 + -ATPase抑制剂(thapsigargin),Ca2 +通道阻滞剂(硝苯地平和Gd3 +)预处理细胞或长时间暴露于高K +(75 mM)培养基中不会改变EqTx-II诱导的Ca2 +信号。据我们所知,这是第一个证明EqTx-II引起神经母细胞瘤细胞肿胀,并且这种作用既与[Ca2 +](i)的增加相关,又需要细胞外Na +的存在。提示EqTx-II具有插入神经母细胞瘤细胞质膜并形成改变膜通透性和细胞内摩尔渗透压浓度的孔的能力,从而引起水大量流入细胞。 (C)2000 Elsevier ScienceLtd。保留所有权利。 [参考:27]

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