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作 者:洪富源[1,2] 孙芳[3] 刘军[3] 姚建[3] 黄一新[3] 唐知还[3]
机构地区:[1]福建医科大学省立临床学院,福州350001 [2]福建省立医院肾内科 [3]上海市第一人民医院肾内科,上海200080
出 处:《中国血液净化》2010年第8期436-440,共5页Chinese Journal of Blood Purification
基 金:福建省科技厅青年创新基金(闽科计[2006]75号)
摘 要:目的观察糖基化终末产物(advanced glycation end products,AGEs)对人腹膜间皮细胞(humanperitoneal mesothelial cell,HPMC)分泌单核细胞趋化蛋白1(monocyte chemoattractant protein-1,MCP-1)的作用及细胞内活性氧族(reactive oxygen species,ROS)在其中的作用。方法分别用不同浓度的糖基化人血清白蛋白(advanced glycation end product s-human serum albumin,AGE HSA)及抗氧化剂N乙酰-L半胱氨酸(N acetyl-L cysteine,NAC)作用于细胞,用逆转录多聚酶链反应(RT PCR)法和酶联免疫吸附法(E L I S A)测定HPMC中MC P 1的表达;再以氧化敏感的荧光染料2,7-二氢二氯荧光素(2,7-dichlorofluorescin,DCFH)染色,流式细胞仪测定ROS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MCP-1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MCP-1的分泌。结论 AGE HSA可能部分通过诱导细胞内ROS,促进HPMC表达MCP-1。Objective To study the effects of advanced glycation end products-human serum albumin (AGE- HSA) on the production of monocyte chemoattractant protein- 1 (MCP- 1) in human peritoneal mesothelial cells (HPMC) and the role of reactive oxygen species (ROS) in this process. Methods AGE-HSA (0, 100, 500 and 1000μg/ mL) with or without 30mM N-acetyl-L-cysteine (NAC) were added to the cell culture medium to stimulate HPMC. MCP-1 mRNA was measured by semi-quantitative RT-PCR, and MCP-1 protein in HPMC was determined by ELISA. The cells were marked with oxidation-susceptible flurorescent probe 2,7-dichorofluoresin diacetate (DCFH) and then were assayed by flow cytometry. Results AGE-HSA increased the concentration of ROS in HPMC with a dose-dependent manner. AGE-HSA also stimulated the production of MCP-1 in dose- and time- dependent manners. The effects of AGE-HSA on HPMC could be blocked by antioxidant NAC. Conclusion The induction of ROS by AGE-HSA in HPMC stimulates the expression of MCP-1. This process may play an important role in the inflammatory reaction and may lead to the ultrafiltration failure.
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