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有机碘对人甲状腺细胞分泌细胞因子IL-6和IL-8的影响 被引量:1

Effect of DIT on cytokines secretion in cultured human thyrocytes
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摘要 目的研究不同浓度的有机碘(DIT)对体外培养的人甲状腺细胞(TEC)分泌细胞因子IL-6和IL-8的影响,并且和无机碘(KI)进行比较,以探讨一种更安全有效的补碘制剂。方法取甲状腺腺瘤旁正常甲状腺组织,应用原代细胞培养技术进行细胞培养,以不同浓度(10^-8~10^-3 mol/L)的DIT和KI刺激单层培养的甲状腺细胞,采用双抗体夹心ELISA法测定各组甲状腺细胞培养上清液中细胞因子IL-6和IL-8的含量。结果正常的甲状腺细胞能分泌少量的IL-6和IL-8。DIT10^-6~10^-3 mol/L浓度组IL-6的分泌量高于正常对照组,10^-4 mol/L、10^-3 mol/L浓度组IL-6的分泌量低于同一浓度的KI组;DIT10^-5~10^-3 mol/L浓度组IL-8的分泌量高于正常对照组,10^-3 mol/L、10^-4 mol/L、10^-3 mol/L浓度组IL-8的分泌量低于同一浓度的KI组。在同一浓度上,DIT组IL-6和IL-8的增加程度低于KI组。结论高碘可刺激甲状腺细胞分泌更多的IL-6和IL-8,而有机碘的安全性相对高于无机碘。 Objective To investigate the influence of DIT on cytokines (IL - 6, IL - 8) secretion of human thyrocytes and compare DIT with KI. To study a good kind of supplement to USI that is safe and effective, Methods The human thyroid epithelium cells from para- adenoma normal tissues from thyroid adenoma patients were cultured in the absence or presence of 10^-8 - 10^-3 mol/L DIT or KI. The contents of cytokines such as IL -6, IL -8 in supernatant of cultured thyrocytes were detected by ELISA method. Results A few IL - 6, IL - 8 were detected in supernatant of normal thyrocytes. IL - 6 in supernatant of DIT group ( 10^-6 - 10^-3 mol/L) increased significantly compared with normal thyrocytes. L - 6 in supernatant of DIT group ( 10^-4 mol/L, 10^-3 mol/L) decreased significantly compared with KI group ( 10^-4 mol/L, 10^-3 mol/L). IL - 8 in supernatant of DIT group ( 10^-5 - 10^-3 mol/L) increased significantly compared with normal thyrocytes. IL - 8 in supernatant of DIT group ( 10^-5 mol/L, 10^-4 mol/L, 10^-3 mol/L) decreased significantly compared with KI group ( 10^-5 mol/L, 10^-4 mol/L, 10^-3 mol/L). In the same contents, IL - 6, IL - 8 in supernatant of DIT group decreased significantly compared with KI group. Conclusion High concentration of iodine can increase cytokines (IL- 6, IL -8) secretion of normal thyrocytes. And DIT has more security than KI.
出处 《中国地方病防治》 北大核心 2007年第5期343-345,共3页 Chinese Journal of Control of Endemic Diseases
基金 山东省卫生厅科研基金资助项目(2001CA1AA18)
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