中国临床医学
中國臨床醫學
중국림상의학
CLINICAL MEDICAL JOURNAL OF CHINA
2014年
3期
259-261
,共3页
吴海波%才志刚%张绍明%张珩%汪雷%徐小平
吳海波%纔誌剛%張紹明%張珩%汪雷%徐小平
오해파%재지강%장소명%장형%왕뢰%서소평
microRNA%HT-29%炎性反应%脂多糖
microRNA%HT-29%炎性反應%脂多糖
microRNA%HT-29%염성반응%지다당
MicroRNA%HT-29%Inflammation%Lipopolysaccharide
目的:研究microRNAs (miRNAs)在脂多糖(LPS)诱导的结肠癌细胞 HT-29炎性反应模型中的表达。方法:用400 ng/mL的LPS处理HT-29细胞48 h ,构建HT-29细胞炎性反应模型(LPS组),将未经LPS处理的 HT-29细胞作为对照组;抽提细胞总RNA ,检测HT-29细胞中白介素-6(IL-6)、C反应蛋白(CRP)的表达水平;用颈环结构引物反转录miRNAs ,应用实时荧光定量PCR测定其表达水平。结果:LPS组中IL-6和CRP的表达较对照组显著升高(P<0.01),表明建模成功。LPS组miR-22、miR-26、miR-214的表达水平较对照组低,而 miR-23的表达水平较对照组高( P<0.05);两组 miR-24、miR-30、miR-181的表达水平差异无统计学意义。结论:miRNAs可能参与LPS诱导的HT-29结肠癌细胞的炎性反应过程。
目的:研究microRNAs (miRNAs)在脂多糖(LPS)誘導的結腸癌細胞 HT-29炎性反應模型中的錶達。方法:用400 ng/mL的LPS處理HT-29細胞48 h ,構建HT-29細胞炎性反應模型(LPS組),將未經LPS處理的 HT-29細胞作為對照組;抽提細胞總RNA ,檢測HT-29細胞中白介素-6(IL-6)、C反應蛋白(CRP)的錶達水平;用頸環結構引物反轉錄miRNAs ,應用實時熒光定量PCR測定其錶達水平。結果:LPS組中IL-6和CRP的錶達較對照組顯著升高(P<0.01),錶明建模成功。LPS組miR-22、miR-26、miR-214的錶達水平較對照組低,而 miR-23的錶達水平較對照組高( P<0.05);兩組 miR-24、miR-30、miR-181的錶達水平差異無統計學意義。結論:miRNAs可能參與LPS誘導的HT-29結腸癌細胞的炎性反應過程。
목적:연구microRNAs (miRNAs)재지다당(LPS)유도적결장암세포 HT-29염성반응모형중적표체。방법:용400 ng/mL적LPS처리HT-29세포48 h ,구건HT-29세포염성반응모형(LPS조),장미경LPS처리적 HT-29세포작위대조조;추제세포총RNA ,검측HT-29세포중백개소-6(IL-6)、C반응단백(CRP)적표체수평;용경배결구인물반전록miRNAs ,응용실시형광정량PCR측정기표체수평。결과:LPS조중IL-6화CRP적표체교대조조현저승고(P<0.01),표명건모성공。LPS조miR-22、miR-26、miR-214적표체수평교대조조저,이 miR-23적표체수평교대조조고( P<0.05);량조 miR-24、miR-30、miR-181적표체수평차이무통계학의의。결론:miRNAs가능삼여LPS유도적HT-29결장암세포적염성반응과정。
Objective:To study the expression of microRNAs (miRNAs) in colon adenocarcinoma cell line HT-29 with lipopo-lysaccharide-induced(LPS-induced) inflammation .Methods :HT-29 cells were treated with 400 ng/mL LPS for 48 h to establish inflammatory HT-29 cell model (LPS group) ,and HT-29 cells without LPS treatment were viewed as the control group .Total RNA from the two groups was isolated with Trizol reagent ,and IL-6 and CRP were examined .The expression of miRNAs was determined by Real-time PCR .Results:Compared with the control group ,the mRNA levels of IL-6 and CRP were up-regulated in LPS group .The expression levels of miR-22 ,miR-26 ,miR-214 in LPS group were lower than those in the control group , while miR-23 level was higher than that in the control group .The levels of miR-24 ,miR-30 and miR-181 were not statistically different between the two groups .Conclusions :MiRNAs may play important roles in LPS-induced inflammation of adenocarci-noma cells .