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内毒素刺激诱导人外周血细胞促炎细胞因子的释放
引用本文:董宁,祝筱梅,张庆红,于燕,张虹,姚咏明.内毒素刺激诱导人外周血细胞促炎细胞因子的释放[J].感染、炎症、修复,2013(3):136-139.
作者姓名:董宁  祝筱梅  张庆红  于燕  张虹  姚咏明
作者单位:[1]解放军总医院第一附属医院全军烧伤研究所,北京100048 [2]解放军61541部队门诊部,北京100094
基金项目:国家自然科学基金项目(81071545,30971192,81130035,81121004);国家重点基础研究发展计划项目(2012CB518102);全军“十二五”计划重大项目(AWS11J008,BWS12J050)
摘    要:目的:探讨内毒素(LPS)体外刺激对人外周血细胞高迁移率族蛋白B1(HMGB1)及肿瘤坏死因子(TNF)-α、白介素(IL)-6和IL-10分泌的影响.方法:采集20例健康志愿者外周血,与培养基等体积混合后体外培养,给予不同浓度LPS(100 ng/ml,500 ng/ml)刺激,分别于刺激后0、2、6、12、24 h收集细胞培养上清液,ELISA法检测其HMGB1和TNF-α、IL-6、IL-10的含量.结果:体外LPS刺激诱导外周血细胞分泌HMGB1增加,12 h后表达持续升高(P〈0.01),分泌水平呈明显时间依赖性;TNF-α、IL-6产生亦呈时间、剂量依赖性,分别于24 h和6~12 h达分泌高峰(P〈0.01);IL-10表达量均较低.结论:TNF-α、IL-6为早期炎症介质,HMGB1为介导内毒素所致迟发死亡的重要晚期炎症介质,它们在脓毒症的发生、发展中可能扮演重要角色.

关 键 词:脂多糖  高迁移率族蛋白B1  肿瘤坏死因子-α  白介素-6

Effects of lipopolysaccharide stimulation on secretion of pro-inflammatory cytokines from mononuclear cells of human peripheral blood
Institution:Dong Ning , Zhu Xiaomei, Zhang Qinghong, et al. Burns Institute, First Hospital Affiliated to the Chinese PLA General Hospital, Beijing 100048,China
Abstract:Objective:To observe the effect of lipopolysaccharide (LPS) stimulation on secretion of high mobility group box-1 protein (HMGB1), tumor necrosis factor-α (TNF-α), interleukin 6 (IL-6) and IL-10 from cells of human peripheral blood in vitro. Methods: Peripheral blood samples were collected from 20 healthy volunteers and cultured with the equal volume of cell culture medium in vitro. After treatment with LPS (100 ng/ml or 500 ng/ml) for 0, 2, 6, 12, or 24 hours, culture supernatants were collected and levels of HMGB1, TNF α, IL-6 and IL-10 were measured with ELISA. Results: A significant release of HMGB1 in human blood was observed after cultured with LPS for 12 hours (P(0. 01), showing a time-dependent response manner. Similarly, production of TNF-α and IL-6 peaked at 24 hours and 6-12 hours in a dose-dependent manner after stimulation with LPS (P〈0. 01). Expression of IL-10 remained in low level after stim- ulation with LPS in various doses. Conclusions: HMGB1 is a late inflammatory factor in inducing the late death as a result of endotoxin challenge. TNF-α and IL-6 are important early pro-inflammatory cytokines acting as the motivator in the de velopment of sepsis. Both early and late pro-inflammatory cytokines appear to be involved in the development of sepsis.
Keywords:Lipopolysaccharide High mobility group box 1 protein Tumor necrosis factor-α Interleukin-6
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