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作 者:万黎[1] 王建军[1] 周雪峰[1] 赵峰[1] 范凯[1]
机构地区:[1]华中科技大学同济医学院附属协和医院胸外科,武汉430022
出 处:《中华实验外科杂志》2010年第3期366-368,共3页Chinese Journal of Experimental Surgery
基 金:教育部博士点基金资助项目(20060487046)
摘 要:目的观察针对半乳糖凝集素(galectin)-3的特异性siRNA对CD133+肺腺癌细胞功能的影响。方法实时荧光定量PCR技术(FQRT.PCR)和Westernblot检测siRNA对galectin.3的干扰效率,噻唑蓝(MTr)比色法检测siRNA对CD133+肺腺癌细胞增殖的影响,AnnexinV和PI双染检测转染siRNA的CD133+肺腺癌细胞上清诱导CD8+T细胞凋亡能力。结果针对galectin-3的siRNA平均干扰效率为80.3%,明显降低CD133+细胞中galeetin-3的表达,并抑制CD133+细胞增殖,转染96h后细胞活率为未转染组的(75.0±3.5)%,凋亡检测结果表明转染siRNA的CD133+肺腺癌细胞上清诱导CD8+T细胞凋亡率为8.2%,与未转染组凋亡率18.6%比较诱导凋亡的能力明显下降,差异有统计学意义(P〈0.05)。结论针对galectin-3的siRNA高效抑制galectin-3的表达,降低细胞的增殖能力及诱导CD8+T细胞凋亡的能力,具有潜在的临床应用价值。Objective To explore the inhibitory effects of specific siRNA targeting galectin-3 on the function of CD133+ lung adenocarcinoma cells. Methods The effect of galectin-3 siRNA was detected by fluorescent quantitative reverse transcription-polymerase chain reaction (FQRT-PCR) and Western blotting, and the inhibitory effect of galectin-3 on the growth of CD133+ lung adenocarcinoma cells was detected by MTT assay. Annexin V and PI test was used to investigate whether supernatants of CD133 + lung adenocarcinoma ceils transfected with siRNA or siRNAmut could mediate apoptosis of CD8 + T ceils in vitro. Results The results of FQRT-PCR revealed that siRNA could interfere with galectin-3 with the interfer- ence efficiency being 80.3%. The Western blotting results showed that siRNA could efficiently depressed the galeetin-3 protein expression and the mutant of siRNA had no effect to interfere with galectin-3. The MTT assay demonstrated that the viability rate of CD133+ cells treated with siRNA was decreased with with time after transfection. At the 96th h after transfection, the viability rate of CD133+ cells treated with siR- NA [ (75.0 ±3.5)% ] was significantly lower than that of CD133+ cells treated with siRNA mutant [ (95.0 ±1.2)% ]. The apoptosis rate of CD8 + T cells induced by the supernatants of CD133 + cells at the 48th h after transfection with siRNA was 8.2% , which was lower than that of CD133 + cells untreated ( 18.6% ) ( P 〈 0.05 ). Conclusion Down-regulation of galectin-3 by siRNA could efficiently reduce the proliferative capacity of CD133 + cells in vitro as well as induce CD8+ T cell apoptosis. These findings indicate Galeetin-3 may play an important role during oncogenesis, implying a potential therapeutic value of siRNA targeting galeetin-3 in clinical practice.
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