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首页> 外文期刊>Academic Journal of Xi'an Jiaotong University >EFFECTS OF ANTISENSE OLIGODEOXYNUCLEOTIDES ON EXPRESSION OF CASPASE-3 IN Γ-RADIATION INDUCED APOPTOTIC HL-60 CELLS
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EFFECTS OF ANTISENSE OLIGODEOXYNUCLEOTIDES ON EXPRESSION OF CASPASE-3 IN Γ-RADIATION INDUCED APOPTOTIC HL-60 CELLS

机译:反义寡聚寡核苷酸对γ射线诱导的凋亡HL-60细胞Caspase-3表达的影响

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摘要

Objective To study the inhibitory effects of caspase-3 mRNA antisense oligodeoxynucleotides (ASODN) on expressions of caspase-3 and it's mRNA in γ-radiation induced apoptotic HL-60 cells, and screen the effective ASODN. Methods ASODN-1 and ASODN-2 targeting 5'-noncoding region and initial translation region of caspase-3 mRNA were respectively designed, synthesized and introduced into HL-60 cells by means of liposome-mediated transfection followed by 10 Gy γ-radiation exposures. TUNEL assay was conducted to investigate the morphologic change and apoptotic percentage of HL-60 cells 18 h later. Immunocytochemical staining and one step RT-PCR were respectively performed to detect the expressions of caspase-3 and it's mRNA. Mismatched oligodeoxynucleotide (MODN) transfected and un-transfected HL-60 cells were taken as control. Results TUNEL assay found that the apoptotic percentages in ASODN-1 and ASODN-2 groups were significantly reduced compared with the control groups (P < 0.01) when the final concentration of both ASODNs was ≥ 3 μmol/L. Immunocytochemistry showed that caspase-3 positive cell percentages were reduced but the average gray values increased significantly compared with the control groups (P < 0.01). RT-PCR showed expressions of caspase-3 mRNA was decreased after ASODN transfection. Furthermore, ASODN-1 proved more effective in inhibiting HL-60 cell apoptosis than ASODN-2 (P < 0.01). Conclusion Caspase-3 mRNA ASODNs can prevent HL-60 cells from apoptosis induced by γ-radiation and reduce expression of caspase-3 and its mRNA. These effects are dose dependent in a certain range.
机译:目的研究caspase-3 mRNA反义寡聚脱氧核苷酸(ASODN)对γ射线诱导的HL-60细胞凋亡的caspase-3及其mRNA表达的抑制作用,并筛选出有效的ASODN。方法分别设计,合成和靶向靶向caspase-3 mRNA 5'-非编码区和起始翻译区的ASODN-1和ASODN-2,并通过脂质体介导的转染,随后10 Gyγ射线照射将其引入HL-60细胞。 TUNEL法检测18小时后HL-60细胞的形态变化和凋亡百分数。分别进行免疫细胞化学染色和一步RT-PCR检测caspase-3及其mRNA的表达。将错配的寡脱氧核苷酸(MODN)转染的和未转染的HL-60细胞作为对照。结果TUNEL法检测到,当两种ASODNs的最终浓度均≥3μmol/ L时,ASODN-1和ASODN-2组的凋亡百分比均显着降低(P <0.01)。免疫细胞化学分析显示,与对照组相比,caspase-3阳性细胞百分比降低,但平均灰度值显着增加(P <0.01)。 RT-PCR显示转染ASODN后caspase-3 mRNA表达降低。此外,ASODN-1被证明比ASODN-2更有效地抑制HL-60细胞凋亡(P <0.01)。结论Caspase-3 mRNA ASODNs可以抑制γ射线诱导的HL-60细胞凋亡,并降低caspase-3及其mRNA的表达。这些作用在一定范围内是剂量依赖性的。

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