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首页> 外文期刊>Biochimica et biophysica acta. Biomembranes >Reciprocal inhibition of Cd2+ and Ca2+ uptake in human intestinal crypt cells for voltage-independent Zn-activated pathways
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Reciprocal inhibition of Cd2+ and Ca2+ uptake in human intestinal crypt cells for voltage-independent Zn-activated pathways

机译:相互抑制人小肠隐窝细胞中Cd2 +和Ca2 +的摄取,以实现电压独立的Zn激活途径

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Cadmium-Ca-Zn interactions for uptake have been studied in human intestinal crypt cells HIEC. Our results failed to demonstrate any significant cross-inhibition between Cd and Ca uptake under single metal exposure conditions. However, they revealed a strong reciprocal inhibition for a Zn-stimulated mechanism of transport. Optimal stimulation was observed under exposure conditions that favor an inward-directed Zn gradient, suggesting activation by extracellular rather than intracellular Zn. The effect of Zn on the uptake of Ca was concentration-dependent, and zinc-induced stimulation of Cd uptake resulted in a 3- and 5.8-fold increase in the K-m and V-max values, respectively. Neither basal nor Zn-stimulated Ca uptakes were sensitive to membrane depolarization. However, the stimulated component of uptake was inhibited by the trivalent cations Gd3+, and La3+ and to a lesser extent by Mg2+ and Ba2+. RT-PCR analysis as well as uptake measurement performed with extracellular ATP and/or suramin do not support the involvement of purinergic P2X receptor channels. Uptake and fluorescence data led to the conclusion that Zn is unlikely to trigger Ca influx in response to Ca release from thapsigargin-sensitive intracellular pools. Our data show that Zn may potentiate Cd accumulation in intestinal crypt cells through mechanism that still needs to be clarified. (c) 2006 Elsevier B.V All rights reserved.
机译:在人体小肠隐窝细胞HIEC中已研究了镉-钙-锌相互作用的摄取。我们的结果未能证明在单一金属暴露条件下Cd和Ca吸收之间有任何明显的交叉抑制作用。但是,他们发现对锌刺激的转运机制有很强的相互抑制作用。在有利于向内的Zn梯度的暴露条件下观察到最佳刺激,表明是通过细胞外而不是细胞内Zn激活。锌对钙吸收的影响是浓度依赖性的,锌诱导的镉吸收刺激导致K-m和V-max值分别增加3倍和5.8倍。基础和锌刺激的钙摄取都不对膜去极化敏感。但是,三价阳离子Gd3 +和La3 +抑制了摄取的刺激成分,而Mg2 +和Ba2 +则抑制了较小程度的摄取。 RT-PCR分析以及用细胞外ATP和/或苏拉明进行的吸收测量均不支持嘌呤能P2X受体通道的参与。吸收和荧光数据得出结论,锌不太可能触发对毒胡萝卜素敏感的细胞内钙释放的钙的流入。我们的数据表明,Zn可能通过尚需阐明的机制来增强Cd在肠隐窝细胞中的蓄积。 (c)2006 Elsevier B.V保留所有权利。

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