牡丹江医学院学报
牡丹江醫學院學報
모단강의학원학보
Journal of Mudanjiang Medical University
2015年
5期
1-4
,共4页
徐舜%黄海姣%李南红%张兵%贾宇斌%杨宇坤%崔红晶%刘新光
徐舜%黃海姣%李南紅%張兵%賈宇斌%楊宇坤%崔紅晶%劉新光
서순%황해교%리남홍%장병%가우빈%양우곤%최홍정%류신광
MicroRNA-33%NIH/3T3细胞%细胞衰老%过氧化氢
MicroRNA-33%NIH/3T3細胞%細胞衰老%過氧化氫
MicroRNA-33%NIH/3T3세포%세포쇠로%과양화경
MicroRNA-33%NIH/3T3cells%Cellular senescence%H2 O2
目的:检测microRNA-33(miR-33)在过氧化氢(H2O2)诱导的NIH/3T3细胞衰老模型中的表达水平,并进一步研究过表达miR-33对H2 O2诱导的细胞衰老的影响。方法 H2 O2处理小鼠胚胎成纤维细胞系NIH/3T3后,利用SA-β-半乳糖苷酶染色以及Western blot检测p16蛋白的表达验证H2 O2诱导NIH/3T3细胞的衰老表型;利用荧光定量PCR检测miR-33在H2 O2诱导的衰老NIH/3T3细胞中的表达;利用RNAimax转染miR-33模拟物Agomir-33及其对照Agomir NC至NIH/3T3细胞,研究过表达miR-33对H2 O2诱导的NIH/3T3细胞衰老表型的影响。结果 miR-33在H2 O2诱导的NIH/3T3细胞衰老模型中显著下调,但过表达miR-33并不显著影响H2 O2诱导的NIH/3T3细胞衰老。结论 MicroRNA-33在过氧化氢诱导的细胞衰老表型中并不发挥显著作用。
目的:檢測microRNA-33(miR-33)在過氧化氫(H2O2)誘導的NIH/3T3細胞衰老模型中的錶達水平,併進一步研究過錶達miR-33對H2 O2誘導的細胞衰老的影響。方法 H2 O2處理小鼠胚胎成纖維細胞繫NIH/3T3後,利用SA-β-半乳糖苷酶染色以及Western blot檢測p16蛋白的錶達驗證H2 O2誘導NIH/3T3細胞的衰老錶型;利用熒光定量PCR檢測miR-33在H2 O2誘導的衰老NIH/3T3細胞中的錶達;利用RNAimax轉染miR-33模擬物Agomir-33及其對照Agomir NC至NIH/3T3細胞,研究過錶達miR-33對H2 O2誘導的NIH/3T3細胞衰老錶型的影響。結果 miR-33在H2 O2誘導的NIH/3T3細胞衰老模型中顯著下調,但過錶達miR-33併不顯著影響H2 O2誘導的NIH/3T3細胞衰老。結論 MicroRNA-33在過氧化氫誘導的細胞衰老錶型中併不髮揮顯著作用。
목적:검측microRNA-33(miR-33)재과양화경(H2O2)유도적NIH/3T3세포쇠로모형중적표체수평,병진일보연구과표체miR-33대H2 O2유도적세포쇠로적영향。방법 H2 O2처리소서배태성섬유세포계NIH/3T3후,이용SA-β-반유당감매염색이급Western blot검측p16단백적표체험증H2 O2유도NIH/3T3세포적쇠로표형;이용형광정량PCR검측miR-33재H2 O2유도적쇠로NIH/3T3세포중적표체;이용RNAimax전염miR-33모의물Agomir-33급기대조Agomir NC지NIH/3T3세포,연구과표체miR-33대H2 O2유도적NIH/3T3세포쇠로표형적영향。결과 miR-33재H2 O2유도적NIH/3T3세포쇠로모형중현저하조,단과표체miR-33병불현저영향H2 O2유도적NIH/3T3세포쇠로。결론 MicroRNA-33재과양화경유도적세포쇠로표형중병불발휘현저작용。
Objective We herein attempted to detect the expression of microRNA-33 (miR-33) in the H2O2 -induced pre-mature senescence of NIH/3T3 cells, and further probed into the role of miR-33 on H2 O2 -induced premature senescence by ectopic expression of miR-33 in NIH/3T3 cells.Methods The senescence-associatedβ-galactosidase staining and the detection of mo-lecular senescencent marker, p16 expression levels by western blot were performed to confirm the premature senescence in NIH/3T3 cells after H2 O2 treatment;Real-time qPCR was utilized to detect the miR-33 expression in H2 O2 -induced premature senescence of NIH/3T3 cells;To investigate into the function of miR-33 on H2 O2 -induced premature senescence, miR-33 mimics ( Agomir 33) or the negative control ( Agomir NC) was trasfected into the NIH/3T3 cells by lipofectamine RNAimax.Results miR-33 was dramatically down-regulated in the H2 O2 -induced premature senescence of NIH/3T3 cells.Nonetheless, forced expression of miR-33 exhibited no significant effect on H2 O2 -induced premature senescence.Conclusion MicroRNA-33 might not play an important role in the H2 O2 -induced premature senescence.