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肝细胞中的微量元素摄取。2. 培养基中不同蛋白质对肝癌细胞摄取铜和锌的影响。

Trace element uptake in liver cells. 2. Effect of different proteins in the medium on the uptake of copper and zinc by hepatoma cells.

作者信息

van den Berg G J, van den Hamer C J

出版信息

J Inorg Biochem. 1985 Aug;24(4):289-97. doi: 10.1016/0162-0134(85)85057-1.

DOI:10.1016/0162-0134(85)85057-1
PMID:4045449
Abstract

Cultured rat hepatoma cells (HTC-cells) were used to study the uptake of copper and zinc from a minimal salt-glucose medium, supplemented with albumin from different species or with ovalbumin. Competitive equilibrium dialysis showed that at low molar ratios of metal/protein (less than 1) the affinity for copper of human and bovine albumin was about equal, but that of dog albumin or ovalbumin was much lower. Only a small difference in affinity for zinc could be detected between human albumin and ovalbumin. Supplementing the medium with the different proteins the rate of copper uptake in the cell at a given molar Cu/protein ratio increased as follows: human albumin congruent to bovine albumin less than dog albumin less than ovalbumin. When the molar Cu/protein ratio was increased, a discontinuity was seen with all three albumin species at a ratio of about 1. In contrast, the zinc uptake mimics that of Cu/ovalbumin, and no discontinuity was observed using different molar Zn/protein ratios. These results indicate that the rate of copper and zinc uptake depends strongly on its affinity for the protein: a low affinity leads to a high uptake. The results suggest further that at physiologic concentrations zinc is taken up by a mechanism different from that for copper.

摘要

培养的大鼠肝癌细胞(HTC细胞)被用于研究从添加了不同物种白蛋白或卵清蛋白的最低盐 - 葡萄糖培养基中摄取铜和锌的情况。竞争性平衡透析表明,在低金属/蛋白质摩尔比(小于1)时,人白蛋白和牛白蛋白对铜的亲和力大致相等,但狗白蛋白或卵清蛋白的亲和力则低得多。在人白蛋白和卵清蛋白之间,仅检测到对锌的亲和力有微小差异。用不同蛋白质补充培养基后,在给定的铜/蛋白质摩尔比下,细胞摄取铜的速率增加如下:人白蛋白≈牛白蛋白<狗白蛋白<卵清蛋白。当铜/蛋白质摩尔比增加时,在约1的比例下,所有三种白蛋白都出现了不连续性。相比之下,锌的摄取情况类似于铜/卵清蛋白的情况,使用不同的锌/蛋白质摩尔比未观察到不连续性。这些结果表明,铜和锌的摄取速率强烈依赖于其对蛋白质的亲和力:低亲和力导致高摄取。结果还进一步表明,在生理浓度下,锌的摄取机制与铜不同。

相似文献

1
Trace element uptake in liver cells. 2. Effect of different proteins in the medium on the uptake of copper and zinc by hepatoma cells.肝细胞中的微量元素摄取。2. 培养基中不同蛋白质对肝癌细胞摄取铜和锌的影响。
J Inorg Biochem. 1985 Aug;24(4):289-97. doi: 10.1016/0162-0134(85)85057-1.
2
Trace metal uptake in liver cells. 1. Influence of albumin in the medium on the uptake of copper by hepatoma cells.肝细胞中的痕量金属摄取。1. 培养基中白蛋白对肝癌细胞摄取铜的影响。
J Inorg Biochem. 1984 Oct;22(2):73-84. doi: 10.1016/0162-0134(84)80016-1.
3
Zinc(II) and copper(II) binding to serum albumin. A comparative study of dog, bovine, and human albumin.锌(II)和铜(II)与血清白蛋白的结合:犬、牛和人白蛋白的比较研究
J Biol Chem. 1994 Oct 14;269(41):25557-61.
4
Copper and zinc ion binding by bovine, dog, and rat serum albumins.牛、犬和大鼠血清白蛋白对铜离子和锌离子的结合
J Inorg Biochem. 1981 Jul;14(4):359-62. doi: 10.1016/s0162-0134(00)80292-5.
5
Mobilization of copper(II) from plasma components and mechanisms of hepatic copper transport.血浆成分中铜(II)的动员及肝脏铜转运机制。
Am J Physiol. 1984 Jan;246(1 Pt 1):G72-9. doi: 10.1152/ajpgi.1984.246.1.G72.
6
Copper is taken up efficiently from albumin and alpha2-macroglobulin by cultured human cells by more than one mechanism.培养的人类细胞可通过多种机制从白蛋白和α2-巨球蛋白中高效摄取铜。
Am J Physiol Cell Physiol. 2008 Sep;295(3):C708-21. doi: 10.1152/ajpcell.00029.2008. Epub 2008 Jun 25.
7
Intrinsic stoichiometric equilibrium constants for the binding of zinc(II) and copper(II) to the high affinity site of serum albumin.锌(II)和铜(II)与血清白蛋白高亲和力位点结合的固有化学计量平衡常数。
J Biol Chem. 1993 Oct 15;268(29):21533-7.
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Copper and zinc toxicity in two rat hepatoma cell lines varying in differentiation.
Comp Biochem Physiol C Comp Pharmacol Toxicol. 1993 Feb;104(2):253-62. doi: 10.1016/0742-8413(93)90032-g.
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Effects of cadmium, copper and metallothionein synthesis inhibiting and stimulating compounds on zinc uptake and accumulation in rat hepatoma HTC cells.镉、铜以及金属硫蛋白合成抑制和刺激化合物对大鼠肝癌HTC细胞锌摄取和积累的影响。
Chem Biol Interact. 1992 Nov 16;84(3):199-220. doi: 10.1016/0009-2797(92)90124-4.
10
Trace element uptake by L-cells as a function of trace elements in a synthetic growth medium.L细胞对微量元素的摄取作为合成生长培养基中微量元素的函数。
J Cell Physiol. 1979 Oct;101(1):57-65. doi: 10.1002/jcp.1041010108.

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