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作 者:洪富源[1] 孙芳[2] 刘军[2] 姚建[2] 黄一新[2] 唐知还[2]
机构地区:[1]福建医科大学省立临床学院福建省立医院肾内科,福州350001 [2]上海市第一人民医院肾内科,上海200080
出 处:《肾脏病与透析肾移植杂志》2008年第6期523-528,共6页Chinese Journal of Nephrology,Dialysis & Transplantation
基 金:福建省科技厅青年创新基金资助(项目编号[2006]F3030)
摘 要:目的:观察糖基化终末产物(AGEs)对人腹膜间皮细胞(HPMC)分泌血管内皮生长因子(VEGF)的影响及细胞内活性氧(ROS)在其中的作用。方法:分别用不同浓度的AGE-HSA及抗氧化剂N-酰-L-半胱氨酸(NAC)作用于细胞,用RT-PCR和ELISA方法测定HPMC中VEGF的表达;再以氧化敏感的荧光染料2、7-二氢二氯荧光素(DCFH)染色,流式细胞仪测定细胞内活性氧强度。结果:AGE-HSA能使细胞内ROS水平明显升高,呈现浓度依赖效应;AGE-HSA同时以时效和量效方式促进HPMC中VEGF的表达;而NAC能够明显抑制AGE-HSA所导致的细胞内ROS升高,同时抑制HPMC中VEGF的分泌。结论:AGE-HSA可能部分通过诱导细胞内ROS,促进HPMC表达VEGF,从而引起腹膜新生血管的增加,最终导致腹膜失超滤现象。Objective : To study the effects of AGE-HSA on the production of VEGF in human peritoneal mesothelial cells (HPMC) in vitro and the role of reactive oxygen species (ROS) in this course. Methodology:The AGE-HSA (0,100,500,1 000 μg/ml) with or without N-acetyl-L-cysteine (NAC 30 mM) were used in culture medium to stimulate the HPMC. The mRNA expression of VEGF was measured with semi-quantitative RT-PCR, moreover, the protein level of VEGF in HPMC was detected by ELISA. The cells were marked with oxidation-susceptible fluroscent probe 2,7-dichorofluoresin diacetate (DCFH) and were assayed by flow cytometry. Results:AGE-HSA increased the concentration of ROS in the HPMC with a dose-dependent manner. AGE-HSA also stimulated the production of VEGF in a dose and time dependent way; the effects of AGE-HSA on HPMC could be blocked by antioxidant NAC. Conclusion:The induction of ROS in HPMC by AGE-HSA, which stimulates the expression of VEGF. It may play an important role in the angiogenesis of peritoneum and leads to ultrafihration failure.
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