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Cellular cadmium uptake mediated by the transport system for manganese.

机译:锰运输系统介导的细胞对镉的吸收。

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The mechanism of cellular cadmium (Cd) uptake has been poorly understood. Recently, we developed Cd-resistant cell lines from metallothionein null mouse cells and showed that the Cd resistance of these cells was conferred primarily by a reduced Cd accumulation. Surprisingly, the uptake rate of manganese (Mn) was also markedly reduced in Cd-resistant cells. Subsequent studies on the kinetics of Cd and Mn uptake by Cd-resistant and parental cells revealed that the Mn transport system with high affinity for Mn is used for cellular Cd uptake, and that this pathway is suppressed in Cd-resistant metallothionein null cells. This is the first indication that the transport system for Mn is used for Cd uptake in mammalian cells. Divalent metal transporter 1 (DMT1) is the only known mammalian transporter involved in the uptake of both Cd and Mn. However, the high-affinity Mn/Cd transport system we found seems to be distinct from DMT1 because of the difference in optimal pH and substrate specificity. On the other hand, various types of Mn transporters have been shown to play an important role in cellular Cd uptake in non-mammalian species such as yeast, plants and bacteria, suggesting the existence of Mn transporters other than DMT1 in mammals.
机译:细胞镉(Cd)摄取的机制了解甚少。最近,我们从金属硫蛋白缺失小鼠细胞中开发了对Cd耐药的细胞系,并表明这些细胞对Cd的耐药性主要是由于减少的Cd积累所致。令人惊讶的是,在耐Cd的细胞中锰(Mn)的摄取率也显着降低。随后对耐Cd和亲代细胞摄取Cd和Mn动力学的研究表明,对Mn具有高亲和力的Mn转运系统可用于细胞吸收Cd,在耐Cd的金属硫蛋白无效细胞中该途径被抑制。这是第一个迹象表明锰的转运系统被用于哺乳动物细胞中的Cd吸收。二价金属转运蛋白1(DMT1)是唯一参与摄取镉和锰的哺乳动物转运蛋白。然而,由于最佳pH和底物特异性的差异,我们发现高亲和力的Mn / Cd转运系统似乎与DMT1不同。另一方面,已表明各种类型的Mn转运蛋白在非哺乳动物物种如酵母,植物和细菌的细胞镉吸收中起重要作用,这表明在哺乳动物中存在除DMT1以外的Mn转运蛋白。

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