Tsuchiya N, Ochi T
Department of Environmental Toxicology, Faculty of Pharmaceutical Sciences, Teikyo University, Kanagawa, Japan.
Arch Toxicol. 1994;68(5):325-31. doi: 10.1007/s002040050077.
The mechanism for the decrease in the accumulation of cadmium (Cd) in Cd-resistant Chinese hamster V79 (Cdr) cells in culture was investigated in a comparison with Cd-sensitive (Cds) cells. Both Cdr and Cds cells took up Cd in a time-dependent manner but the rate of uptake of Cd by Cdr cells was about 15% of that by Cds cells. Kinetic studies of the uptake of Cd showed that the Vmax values for Cdr and Cds cells were 0.31 and 0.46 pmol Cd/h per mg protein, respectively. The Km values were 31.95 microM for Cdr cells and 3.15 microM for Cds cells. Mersalyl acid, a sulfhydryl (SH) blocker to which cells are impermeable, inhibited the uptake of Cd by Cds cells at subtoxic concentrations while Cdr cells were insensitive to inhibition by mersalyl acid, suggesting that SH groups in the plasma membrane play a role in the uptake of Cd. Uptake of Cd by Cds cells was dependent on the pH of the incubation medium and the rate of uptake was very high at pH 7.4 and pH 8.0 relative to the rates at pH 6.0 and pH 6.8. By contrast, the uptake of Cd by Cdr cells was lower at all pH values than that by Cds cells. The decrease in the rate of uptake of Cd by Cdr cells could not be ascribed to an increase in the efflux of Cd. A Cd-blotting technique was used to detect plasma membrane proteins with high affinity for Cd. Two major differences in terms of Cd-binding proteins (Cd-BPs) were observed between Cdr and Cds cells. A 110-kDa Cd-BP, detected in Cds cells, was found at a reduced level in Cdr cells, while an 82-kDa Cd-BP, which was not observed in Cds cells, was detected in Cdr cells.
通过与镉敏感(Cds)细胞对比,研究了培养的耐镉中国仓鼠V79(Cdr)细胞中镉(Cd)积累减少的机制。Cdr和Cds细胞均以时间依赖性方式摄取Cd,但Cdr细胞摄取Cd的速率约为Cds细胞的15%。Cd摄取的动力学研究表明,Cdr和Cds细胞的Vmax值分别为每毫克蛋白质0.31和0.46 pmol Cd/h。Km值对于Cdr细胞为31.95 microM,对于Cds细胞为3.15 microM。汞撒利酸是一种细胞不可渗透的巯基(SH)阻断剂,在亚毒性浓度下抑制Cds细胞摄取Cd,而Cdr细胞对汞撒利酸的抑制不敏感,这表明质膜中的SH基团在Cd摄取中起作用。Cds细胞摄取Cd取决于孵育培养基的pH值,在pH 7.4和pH 8.0时摄取速率相对于pH 6.0和pH 6.8时非常高。相比之下,Cdr细胞在所有pH值下摄取Cd均低于Cds细胞。Cdr细胞摄取Cd速率的降低不能归因于Cd外流的增加。采用镉印迹技术检测对Cd具有高亲和力的质膜蛋白。在Cdr和Cds细胞之间观察到了镉结合蛋白(Cd-BPs)方面的两个主要差异。在Cds细胞中检测到的一种110-kDa的Cd-BP在Cdr细胞中的水平降低,而在Cds细胞中未观察到的一种82-kDa的Cd-BP在Cdr细胞中被检测到。