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作 者:刘学[1] 张馨月[1] 吴秀萍[1] 白雪[1] 李慧萍[1] 郭恒 孙树民[3] 王学林[1] 刘明远[1]
机构地区:[1]吉林大学人畜共患病研究所、人兽共患病研究教育部重点实验室,吉林长春130062 [2]二炮装备研究院,北京100085 [3]内蒙古民族大学动物科技学院,内蒙古通辽028000
出 处:《中国预防兽医学报》2012年第8期611-614,共4页Chinese Journal of Preventive Veterinary Medicine
基 金:国家自然科学基金(30972177)
摘 要:为研究喜树碱(CPT)对小鼠成纤维细胞NIH/3T3中Toll样受体3(TLR3)的表达及活化的影响,本实验利用CCK-8试剂盒测定了CPT在不同浓度下、不同作用时间对NIH/3T3细胞的毒性作用,并确定CPT对NIH/3T3细胞的基本无毒浓度为1μg/mL。通过流式细胞术检测CPT作用NIH/3T3细胞表明,TLR3平均荧光强度与对照组相比显著增强,表明TLR3表达增加。此外,ELISA试剂盒检测结果显示CPT作用后IFN-β表达量增加,并高于阳性对照组,差异极显著(p<0.01)。本研究表明CPT对NIH/3T3细胞的TLR3具有显著的激动作用。To study the effect of CPT on TLR3 expression and activation in mouse fibroblast NIH/3T3 cell. CCK-8 was used to test toxicity of CPT to NIH/3T3 cell at different concentration and different time, and 1 ug/mL of CPT was determined as the basic non-toxic concentration. The FACS result indicated that, compared with negative control group, the statistical of mean fluorescence intensity that cell co-culture with CPT is significantly enhanced after the cell co-cultured with CPT. It showed that the expression of TLR3 was increased in the cells. Furthermore, compared with positive control, expression of IFN-β was increased significantly (p〈0.01) after co-culture with CPT detected by ELISA kit. The present study demonstrated that CPT was able to be as TLR3 agonist in NIH/3T3 cell.
分 类 号:S852.4[农业科学—基础兽医学]
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