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铜和锌对人外周血单核细胞细胞因子分泌的不同影响。

Differential effects of copper and zinc on human peripheral blood monocyte cytokine secretion.

作者信息

Scuderi P

机构信息

Department of Anatomy, University of Arizona, Tucson 85724.

出版信息

Cell Immunol. 1990 Apr 1;126(2):391-405. doi: 10.1016/0008-8749(90)90330-t.

DOI:10.1016/0008-8749(90)90330-t
PMID:2107032
Abstract

The addition of copper and zinc salts to human peripheral blood leukocytes cultured in complete medium containing endotoxin and fetal calf serum stimulated tumor necrosis factor (TNF) secretion in a concentration-dependent manner. The secretion of interleukin-1 beta (IL-1 beta) and interleukin-6 (IL-6) was inhibited by copper under the same culture conditions, while zinc stimulated IL-1 beta secretion in a concentration-dependent manner and had no effect on leukocyte IL-6 release. Both copper and zinc induced increases in TNF mRNA (54 and 14%, respectively) when compared to cells cultured in complete medium alone. In serum-free, low endotoxin medium (less than 6 pg/ml), both copper and zinc failed to stimulate either TNF or IL-1 beta secretion. Under the same conditions the addition of lipopolysaccharide (LPS), at concentrations above 0.01 micrograms/ml, induced a concentration-dependent release of both cytokines. When either copper or zinc were combined with 0.01 micrograms/ml LPS, a synergistic stimulation of TNF secretion resulted. IL-1 beta secretion, unlike TNF, was not synergistically stimulated by combining metals and LPS in serum-free medium. Combining copper and zinc with inhibitors of TNF secretion, transforming growth factor beta, prostaglandin E2, and plasma alpha-globulins, resulted in a reduction of the suppressive effects of each of these agents. This study suggests that the trace metals copper and zinc may play important and possibly distinct roles in regulating leukocyte secretion of TNF, IL-1 beta, and IL-6.

摘要

在含有内毒素和胎牛血清的完全培养基中培养的人外周血白细胞中添加铜盐和锌盐,可呈浓度依赖性刺激肿瘤坏死因子(TNF)的分泌。在相同培养条件下,铜抑制白细胞介素-1β(IL-1β)和白细胞介素-6(IL-6)的分泌,而锌呈浓度依赖性刺激IL-1β的分泌,对白细胞IL-6的释放无影响。与仅在完全培养基中培养的细胞相比,铜和锌均能诱导TNF mRNA增加(分别增加54%和14%)。在无血清、低内毒素培养基(低于6 pg/ml)中,铜和锌均未能刺激TNF或IL-1β的分泌。在相同条件下,添加浓度高于0.01微克/毫升的脂多糖(LPS)可诱导两种细胞因子呈浓度依赖性释放。当铜或锌与0.01微克/毫升LPS联合使用时,可协同刺激TNF的分泌。与TNF不同,在无血清培养基中,金属与LPS联合使用不会协同刺激IL-1β的分泌。将铜和锌与TNF分泌抑制剂、转化生长因子β、前列腺素E2和血浆α球蛋白联合使用,可降低这些药物各自的抑制作用。本研究表明,痕量金属铜和锌可能在调节白细胞TNF、IL-1β和IL-6的分泌中发挥重要且可能不同的作用。

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