中国组织工程研究2016，Vol.20Issue(37)：5552-5559,8.DOI:10.3969/j.issn.2095-4344.2016.37.012
南蛇藤素可抑制肿瘤坏死因子α诱导RAW264.7细胞的炎症及增殖
Celastrol inhibits tumor necrosis factor-alpha induced proliferation and inflammatory responses in RAW264.7 cells
摘要
Abstract
BACKGROUND:Celastrol is one of the active components extracted from the traditional Chinese medicine Celastrus orbiculatus characterized by expel ing the wind and promoting blood circulation and relieving swel ing and pain. <br> OBJECTIVE:To investigate the effects of celastrol on tumor necrosis factor-α(TNF-α) induced proliferation and inflammatory responses in RAW264.7 cel s. <br> METHODS:In vitro inflammatory cel models induced by TNF-α(0, 1, 10, 100μg/L) were treated with celastrol (0.1, 0.5, 1.0, 2.0μmol/L). Interleukin-1β,-6,-8 and prostaglandin E2 in the models were measured by enzyme-linked immunosorbent assay. Cel survival was determined by cel counting kit-8. The inflammatory mediator nitric oxide secretion was detected by nitrate reductase assay. mRNA expressions of inducible nitric oxide synthase, cyclin D1 and cyclin E1 were detected by real-time polymerase chain reaction technique. <br> RESULTS AND CONCLUSION:Significantly increased secretion of interleukin-1β,-6,-8, prostaglandin E2 and nitric oxide, cel proliferation, and mRNA expressions of inducible nitric oxide synthase, cyclin D1 and cyclin E1 were observed after the induction of TNF-α(0.1, 10, 100μg/L) compared with the control group (without the induction of TNF-α) (P<0.05);especial y, 10μg/L of TNF-αexhibited the strongest effects. 0.4μmol/L celastrol significantly suppressed TNF-α-induced release of interleukin-1β,-6,-8, prostaglandin E2 and nitric oxide, cel proliferation, and mRNA expressions of inducible nitric oxide synthase, cyclin D1 and cyclin E1 in RAW264.7 cel s (P<0. 05). Our results demonstrate that celastrol can inhibit TNF-α-induced inflammatory response and proliferation in RAW264.7 cel s.关键词
组织构建/组织工程/南蛇藤素/RAW264.7细胞/肿瘤坏死因子α/炎症/炎症因子/增殖/细胞周期蛋白D1/细胞周期蛋白E1分类
医药卫生引用本文复制引用
陈光福,郭远清,伍玉甜..南蛇藤素可抑制肿瘤坏死因子α诱导RAW264.7细胞的炎症及增殖[J].中国组织工程研究,2016,20(37):5552-5559,8.基金项目
珠海市科技计划(2014D0401990016)Funding:the Science and Technology Planning Project of Zhuhai, China, No.2014D0401990016 （2014D0401990016）
