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作 者:刘峰[1] 姚咏明[1] 董宁[1] 于燕[1] 盛志勇[1]
机构地区:[1]解放军总医院第一附属医院全军烧伤研究所基础部,北京100037
出 处:《中华急诊医学杂志》2008年第2期119-122,共4页Chinese Journal of Emergency Medicine
基 金:国家重点基础研究发展规划项目(2005cB522602);国家自然科学基金资助项目(30672178)
摘 要:目的观察高迁移率族蛋白B1(HMGB1)对小鼠腹腔巨噬细胞肿瘤坏死因子(TNF)-α、白细胞介素(IL)-10及细胞间黏附分子-1(ICAM-1)表达的影响。方法分离小鼠腹腔巨噬细胞,经不同质量浓度(0、1、10、100、1000ng/m1)HMGB1的刺激,于不同时间点(0、6、12、24、48、72h)采用实时荧光定量PCR方法测定细胞TNF-α、IL-10及ICAM-1mRNA表达的变化,同时应用酶联免疫吸附试验检测细胞培养上清液中TNF-α、IL-10以及sICAM-1蛋白水平的变化。数据采用单因素方差分析。结果1~1000ng/ml的HMGB1作用24h,可使巨噬细胞的TNF-α、ICAM-1基因表达增加,与对照组比较差异具有统计学意义(P〈0.01),其中1000ng/ml HMGB1的作用最强,呈剂量一效应关系。而IL-10仅在1000ng/ml HMGB1作用时表达有所增加。以100ng/ml的 HMGB1作用不同时问后,培养上清液TNF-α与sICAM-1的浓度48h达高峰(P〈0.01),呈时间一效应关系,HMGB1对巨噬细胞TNF-α的分泌呈“双峰”特征,而IL-10水平无明显变化。结论一定浓度的HMGB1可诱导巨噬细胞合成、释放促炎细胞因子与黏附分子,具有显著的促炎特性。Objective To investigate the differential expression of tumor necrosis faetor-α (TNF-α), interleukin-10 (IL-10), and intereellular adhesion molecule-1 (ICAM-1) in response to high mobility group box-1 protein (HMGB1) in murine peritoneal macrphage. Meethod The peritoneal maerophages were obtained from female BALBe mice. After exposure to various concentration of HMGB1 (0, 1, 10, 100, 1000 ng/ml), four various lengths of time (0, 6, 12, 24, 48, 72 hours), the maerophages were denatured in cell culture plates to determine mRNA expressions of TNF-α, 1L-10 as well as ICAM-1 by using real-time quantitative PCR, and cell supernatants were harvested to determine the protein levels of TNF-α, IL-10 as well as sICAM-1 by ELISA. Statistical evaluation of data was performed by one-way 'analysis of variance ( ANOVA). Results The protein and gene expressions of TNF-α and ICAM-1/sICAM-1 in peritonael maccrphage were markedly up-regulated by treatment with HMGB1, except for IL-10. Effects of HMGB1 on TNF-α and ICAM-1/sICAM-1 expressions were in a dose-dependent manner, ranged from 1 ng/ml to 1000 ng/ml ( P 〈 0.01 ). The effects of HMGB1 on TNF-α and ICAM-1/sICAM-1 protein and gene expressions were also time-dependent with a significant increase at 48 hours (P 〈 0.01). HMGB1 induced a biphasie response of TNF-α, the first peak approximately 6 hours and the second peak at 24 hours after exposure. However, there was no marked changes in IL-10 gene and protein expressions noted in peritoneal macrophages stimulated with HMGB1. Conclusions HMGB1 appears to be a proinflammatory cytokine, and promotes the synthesis as well as release of TNF-α and ICAM-1, except for IL-10.
关 键 词:高迁移率族蛋白B1 释放促炎细胞因子 小鼠巨噬细胞 黏附分子表达 小鼠腹腔巨噬细胞 sICAM-1 ICAM-1基因表达 细胞培养上清液
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