Zhang Ying, Li Wei-dong, Chi Chun-xin
Department of Gynecology and Obstetrics, Xiaolan People's Hospital, Zhongshan 528415, China.
Nan Fang Yi Ke Da Xue Xue Bao. 2008 Dec;28(12):2253-6.
To study the effect of progesterone on interleukin-6 (IL-6) release from human umbilic vein endothelial cells (HUVECs) induced by high mobility group box-1 protein (HMGB1).
The recombinant expression plasmid pET14b-HMGB1 was constructed and transformed into competent E.coli BL21 cells to obtain HMGB1 protein, which was purified with chromatography on Ni-NTA Sepharose column. Cultured HUVECs were treated with purified HMGB1 protein alone at the concentrations 0, 10, 100, 500, and 1000 ng/ml, progesterone alone at the concentrations of 0, 0.1, 1, 10, 100 mmol/L, or with both HMGB1 protein (500 ng/ml) and progesterone at the terminal concentrations of 0, 0.1, 1, 10, and 100 mmol/L. Twenty-four hours later, the supernatant of the cell culture medium was collected to detect the levels of IL-6 using enzyme-linked immunosorbent assay (ELISA).
The IL-6 levels in HUVEC culture medium was slightly decreased after treatment with low-concentration HMGB1 but increased obviously following treatment with high-concentration HMGB1, and these effects could be dose-dependently inhibited by progesterone. Progesterone alone did not result in any noticeable changes of IL-6 levels in the cell culture medium.
Progesterone can dose-dependently inhibit HMGB1-induced IL-6 release from HUVECs, suggesting the protective role of progesterone in endotoxemia.
研究孕酮对高迁移率族蛋白B1(HMGB1)诱导的人脐静脉内皮细胞(HUVECs)释放白细胞介素-6(IL-6)的影响。
构建重组表达质粒pET14b-HMGB1并转化至感受态大肠杆菌BL21细胞中以获得HMGB1蛋白,该蛋白经镍-亚氨基二乙酸琼脂糖凝胶柱层析纯化。将培养的HUVECs分别用浓度为0、10、100、500和1000 ng/ml的纯化HMGB1蛋白单独处理,用浓度为0、0.1、1、10、100 mmol/L的孕酮单独处理,或用终浓度为0、0.1、1、10和100 mmol/L的HMGB1蛋白(500 ng/ml)与孕酮共同处理。24小时后,收集细胞培养基上清液,采用酶联免疫吸附测定(ELISA)法检测IL-6水平。
低浓度HMGB1处理后HUVEC培养基中的IL-6水平略有下降,但高浓度HMGB1处理后明显升高,而这些效应可被孕酮剂量依赖性抑制。单独使用孕酮未导致细胞培养基中IL-6水平出现任何明显变化。
孕酮可剂量依赖性抑制HMGB1诱导的HUVECs释放IL-6,提示孕酮在内毒素血症中具有保护作用。