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铜对人类肠道上皮Caco-2细胞的毒性研究 被引量:11

Toxicological effects of copper on human intestinal Caco-2 cells
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摘要 目的 了解铜对人类肠道上皮Caco 2细胞的毒性影响。方法 应用噻唑蓝 (MTT)实验、P 糖蛋白(P gp)活性检测实验、活性氧检测及克隆形成实验研究铜对肠道上皮Caco 2细胞的毒性及可能作用机制 ,同时利用Caco 2细胞和肠炎沙门氏菌为模型 ,研究铜对Caco 2细胞对细菌侵入和存活易感性的影响。结果 在一定的暴露场景下 ,铜可明显地降低细胞的活力 ,抑制细胞膜表面P gp的活性 ,促进细胞内活性氧自由基的产生 ,降低细胞的克隆形成能力。此外 ,细胞经铜暴露后 ,肠炎沙门氏菌侵入细胞的数量增加 ,但细胞内存活的细菌数量却下降。结论 过量的铜可导致Caco 2细胞氧化损伤 ,从而引起更广泛的细胞毒性效应 ,但其对细胞对细菌侵入和存活易感性的影响有待进一步研究。 Objective To study the toxicological effects of copper on human intestinal Caco-2 cells.Methods The effects of copper on human intestinal Caco-2 cells were evaluated by MTT conversion, intra-cellular production of reactive oxygen species (ROS), cloning efficiency and changes of P-glycoprotein (P-gp) activities in Caco-2 cells. In addition, Caco-2 cells and Salmonella enteritidis served as the models to examine the effect of copper on the host-parasite interaction. Results Copper induced a dose-dependent decrease of cell viability measured by MTT assay; by using the fluorescent probe 2,7-dichlorofluorescin diacetate, a significant increase of ROS production in Cu-treated cells was detected; the significant time- and dose-dependent decrease of P-gp activities in Cu-treated cells was demonstrated by increased accumulation of rhodamine 123 in cells. Copper treatment also increased the efficiency of the bacterial invasion, but decreased the number of bacteria surviving in the intracellular environment. Conclusion Copper induced a variety of toxicological endpoints which might be caused by oxidative damage, but the effect of copper on cell-bacteria interaction needs to be further investigated.
出处 《卫生研究》 CAS CSCD 北大核心 2004年第3期284-287,共4页 Journal of Hygiene Research
基金 国际铜业协会 (ICA)资助项目 (No .TPT0 542E)
关键词 Caco—2细胞 毒性 细菌 copper, Caco-2 cells, toxicity, bacteria
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参考文献9

  • 1WHO/IPCS. Environmental Health Criteria 200, Copper. Geneva: World Health Organization, 1998,28
  • 2Araya M, McGoldrick MC, Klevay LM, et al. Determination of an acute no-observed-adverse-effect level (NOAEL) for copper in water. Regul Toxicol Pharmacol,2001, 34:137-145
  • 3Zastre J, Jackson J, Bajwa M, et al. Enhanced cellular accumulation of a P-glycoprotein substrate, rhodamine-123, by Caco-2 cells using low molecular weight methoxypolyethylene glycol-block-polycaprolactone diblock copolymers. Eur J Pharma and Biopharma,2
  • 4Hirsch-Ernst KI, Kietzmann T, Ziemann C, et al. Physiological oxygen tensions modulate expression of the mdr1b multidrug-resistance gene in primary rat heptocyte culture. Biochem J, 2000, 350:443-451
  • 5Yang CF, Shen HM, Shen Y, et al. Cadmium-induced oxidative cellular damage in human fetal lung fibroblasts ( MRC-5 cells). Environ Health Perspect, 1997, 105:712-716
  • 6Elsinghorst ER, Baron LS, Kopecko DJ. Penetration of human epithelial cells by Salmonella: molecular cloning.and expression of Sahmonella typhi invasion determinants in Escherichia coli. Proc Natl Acad Sci, 1989,86:5173-5177
  • 7Tertera C, Metcalf ES. Osmolarity and growth phase overlap in regulation of Salmonella typhi adherence to and invasion of human intestinal cells.Infect Immun, 1993,61:3084-3089
  • 8Foster SL, Richardson SH, Failla ML. Elevated iron status increases bacterial invasion and survival and alters cytokine/chemokine mRNA expression in Caco-2 hunan intestinal cells. Am J Nutr,2001,131: 1452-1458
  • 9Abu-Qare AW, Elmasry E, Abou-Donia MB. A role for P-glycoprotein in environmental toxicology. J Toxicol Environ Health Part B,2003,6:279

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