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硫酸乙酰肝素链增强了培养的血管内皮细胞中镉的细胞毒性。

Heparan sulfate chains potentiate cadmium cytotoxicity in cultured vascular endothelial cells.

机构信息

Department of Environmental Health, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, 1432-1 Horinouchi, Hachioji, 192-0392, Japan.

Department of Environmental Health, Faculty of Pharmaceutical Sciences, Toho University, 2-2-1 Miyama, Funabashi, 274-8510, Japan.

出版信息

Arch Toxicol. 2016 Feb;90(2):259-67. doi: 10.1007/s00204-014-1420-6. Epub 2014 Nov 25.

Abstract

The monolayer of vascular endothelial cells, which is rich in heparan sulfate chains, is an important target of cadmium cytotoxicity. To investigate the effects of heparan sulfate chains on cadmium cytotoxicity, bovine aortic endothelial cells were cultured in the presence of cadmium, with or without exogenous heparan sulfate. The following results were obtained: (1) Heparan sulfate chains potentiated cadmium cytotoxicity. (2) Such a potentiation did not occur in bovine aortic smooth muscle cells. (3) Heparin chains as well as heparan sulfate chains potentiated cadmium cytotoxicity, while other glycosaminoglycan chains failed to exhibit such an activity. (4) The disaccharide units of heparan sulfate chains did not potentiate cadmium cytotoxicity in the endothelial cells. (5) Heparan sulfate chains did not potentiate mercury and arsenite cytotoxicity. (6) Fibroblast growth factor-2 (FGF-2) also potentiated cadmium cytotoxicity in the endothelial cells. (7) Heparan sulfate chains significantly increased intracellular cadmium accumulation by inducing the expression of metallothionein. Taken together, these results suggest that heparan sulfate chains activate FGF-2, which in turn elevates the expression and/or activity of metal transporter(s) that facilitate cadmium influx from the extracellular space into the cytoplasm.

摘要

富含硫酸乙酰肝素链的单层血管内皮细胞是镉细胞毒性的重要靶点。为了研究硫酸乙酰肝素链对镉细胞毒性的影响,将牛主动脉内皮细胞在镉存在或不存在外源性硫酸乙酰肝素的情况下进行培养。得到以下结果:(1)硫酸乙酰肝素链增强了镉的细胞毒性。(2)这种增强作用在牛主动脉平滑肌细胞中没有发生。(3)肝素链和硫酸乙酰肝素链增强了镉的细胞毒性,而其他糖胺聚糖链则没有表现出这种活性。(4)硫酸乙酰肝素链的二糖单位在内皮细胞中没有增强镉的细胞毒性。(5)硫酸乙酰肝素链没有增强汞和亚砷酸盐的细胞毒性。(6)成纤维细胞生长因子-2(FGF-2)也增强了内皮细胞中镉的细胞毒性。(7)硫酸乙酰肝素链通过诱导金属硫蛋白的表达,显著增加了细胞内镉的积累。综上所述,这些结果表明,硫酸乙酰肝素链激活了 FGF-2,进而增加了金属转运体的表达和/或活性,促进了镉从细胞外空间进入细胞质。

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