雷公藤甲素抑制PBMC分泌IL-1β蛋白量与IL-1β基因多态性有关(英文)  被引量:1

Inhibitory effect of triptolide on production of IL-1β from PBMC is associated with IL-1β gene polymorphism

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作  者:盛冬云[1] 涂胜豪[1] 陈红波[1] 胡永红[1] 

机构地区:[1]华中科技大学同济医学院附属同济医院中西医结合研究所,湖北武汉430030

出  处:《中国病理生理杂志》2007年第1期90-94,共5页Chinese Journal of Pathophysiology

基  金:Supported by National Natural Science Foundation of China(No.90209049)

摘  要:目的:探讨雷公藤甲素对外周血单个核细胞(PBMC)分泌白细胞介素-1β(IL-1β)的抑制作用与IL-1β基因多态性的关系。方法:采用PCR-RFLP法对31名健康志愿者IL-1β基因启动子区-511位点C-T多态性进行基因型检测,同时进行PBMC培养,用脂多糖(LPS)刺激培养细胞,并予以雷公藤甲素处理PBMC,收集培养上清液,ELISA法检测上清液中IL-1β的含量。结果:携带IL-1β-511T/T纯合子基因型PBMC经LPS刺激后IL-1β的分泌量明显较非T/T纯合子为高(P<0.05);雷公藤甲素能显著抑制LPS诱导的C/C和C/T基因型PB-MC分泌IL-1β(P<0.05),但对T/T基因型的抑制作用不明显(P>0.05)。结论:IL-1β基因-511C-T多态性与IL-1β的分泌量相关,雷公藤甲素对不同基因型的IL-1β抑制作用有差异,这可能是导致雷公藤药理作用出现个体差异的原因之一。AIM: To explore whether the inhibitory effect of triptolide on IL - 1β production by PBMC is associated with IL - 1β gene polymorphisms. METHODS: IL - 1β gene polymorphism was analyzed in 31 healthy volunteers. From genomic DNA, the C -T polymorphism at IL - 1β -511 was typed by PCR - RFLP. Meanwhile the IL - 1β was also measured in the supernatants of the cultured and stimulated peripheral blood mononuclear cells (PBMC) by ELISA. RESULTS: After LPS stimulation in PBMC cultures of healthy subjects, the secretion levels of IL - 1β in 9 volunteers who carried IL - 1β - 511 T/T genotype were higher than in volunteers who are not T/T genotype ( P 〈 0. 05 ). Triptolide suppressed the production of IL - 1β significantly in LPS - treated hnman PBMC carried C/C and C/T genotype ( P 〈 0. 05 ), but this signitleant inhibitory effect of triptolide was not seen in T/T genotype ( P 〉 0. 05 ). CONCLUSION: The gene polymorphism at IL- 1β -511 was related to the production oflL - 1β, and the inhibitory effect of triptolide on the production of IL - 1β was different in C/C, C/T, T/T genotype of IL - 1β -511, which may be one of the reasons for the phenomenon that people respond differently to triptolide.

关 键 词:白细胞介素1 基因 多态现象(遗传学) 雷公藤属 关节炎 类风湿 

分 类 号:R363[医药卫生—病理学]

 

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