Zhu Zhen-dong, Yu Zhuo, Zhang Xuan, Wang Yong-jin, Wang Dian-hua
Kunming Medical University, Kunming 650031, China.
Nan Fang Yi Ke Da Xue Xue Bao. 2011 Jan;31(1):1-4.
To investigate the effect of ADMA on macrophage migration inhibitory factor (MIF) expression and tumor necrosis factor-α (TNF-α) and IL-8 secretion in THP-1 monocyte-derived macrophages. METHIDS: THP-1 monocytes were induced to differentiate into macrophages by a 24-h incubation with 160 nmol/L PMA. The THP-1 monocyte-derived macrophages were exposed to different concentrations of ADMA for 24 h, and the changes in MIF mRNA and protein expressions were analyzed with RT-PCR and Western blotting, respectively. Enzyme-linked immunosorbent assay was used to detect the levels of TNF-α and IL-8 in the supernatant of THP-1-derived macrophages following ADMA treatments.
ADMA obviously up-regulated MIF mRNA and protein expressions in THP-1-derived macrophages in a concentration- dependent manner. Exposure of the cells to 15 µmol/L ADMA for 24 h showed the most potent effect in up-regulating MIF mRNA and protein expressions. ADMA treatment also resulted in a dose-dependent increase of the levels of TNF-α and IL-8 in the culture supernatant of the macrophages, and the peak levels occurred following the treatment with 15 µmol/L ADMA.
ADMA can up-regulate MIF expression and induce TNF-α and IL-8 secretion in THP-1 monocyte-derived macrophages.
研究不对称二甲基精氨酸(ADMA)对THP-1单核细胞来源巨噬细胞中巨噬细胞移动抑制因子(MIF)表达以及肿瘤坏死因子-α(TNF-α)和白细胞介素-8(IL-8)分泌的影响。方法:用160 nmol/L佛波酯(PMA)孵育THP-1单核细胞24小时,诱导其分化为巨噬细胞。将THP-1单核细胞来源的巨噬细胞暴露于不同浓度的ADMA中24小时,分别用逆转录-聚合酶链反应(RT-PCR)和蛋白质免疫印迹法分析MIF mRNA和蛋白表达的变化。采用酶联免疫吸附测定法检测ADMA处理后THP-1来源巨噬细胞上清液中TNF-α和IL-8的水平。
ADMA明显上调THP-1来源巨噬细胞中MIF mRNA和蛋白表达,呈浓度依赖性。细胞暴露于15 µmol/L ADMA 24小时对上调MIF mRNA和蛋白表达的作用最强。ADMA处理还导致巨噬细胞培养上清液中TNF-α和IL-8水平呈剂量依赖性增加,15 µmol/L ADMA处理后达到峰值水平。
ADMA可上调THP-1单核细胞来源巨噬细胞中MIF表达,并诱导TNF-α和IL-8分泌。