首页> 外文期刊>中国癌症研究(英文版) >EFFECTS OF PML AND PML/RMRa ANTISENCE OLIGO- NUCLEOTIDE ON PROMYELOCYTIC rnLEUKEMIA CELL NB4
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EFFECTS OF PML AND PML/RMRa ANTISENCE OLIGO- NUCLEOTIDE ON PROMYELOCYTIC rnLEUKEMIA CELL NB4

机译:PML和PML / RMRa反义寡核苷酸对早幼粒细胞白血病NB4的影响

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Objective: To investigate the effects of anti-PML (promyelocytic leukemia) or anti-PML/RARa (promyelocytic leukemia/retionic acid receptora) antisense oligonucleotides on cell growth, expression of PML-RARa mRNA and PML-RARa/PML protein location of NB4 cell lines. Methods: RT-PCR was used for detecting PML-RARa mRNA expression, trypan blue exclusion for cell count, methylcellose assay for leukemic colony forming unit detection, immuno- fluorescence for PML-RARa/PML protein location. Results: Both anti-PML start codon region antisence (STAS) and anti-PML-RARa fusion region antisence (FUAS) could inhibit cell growth and the formation of acute myelocytic colony forming unit of cells(AML-CFU). Cells become partial differentiated at days 5, being more obvious in FUAS-treated cells than in STAS ones. Down regulation of PML-RARa mRNA expression occurred at 24 hours in STAS and FUAS-treated cells and maintained for up to 72 hours. Immuno-fluorescence analysis with anti-PML monoclonal antibody showed a remarkable decrease even complete disappearance of microgranules. The residual granules became enlarged as discrete dots (<10 per cell), similar to normal POD structure in some STAS-treated cells at 24 hours. At 72 hours, nearly all the granules disappeared. Similar changes were observed in FUAS-treated cells. Conclusion: Both PML and PML-RARa antisence oligonucleotides can specially block the expression of PML-RARa at mRNA and protein levels. PML protein is implicated in the regulations of cell differentiation.
机译:目的:研究抗PML(早幼粒细胞白血病)或抗PML / RARa(早幼粒细胞白血病/视网膜酸受体a)反义寡核苷酸对NB4细胞生长,PML-RARa mRNA表达和PML-RARa / PML蛋白位置的影响细胞系。方法:RT-PCR检测PML-RARa的mRNA表达,锥虫蓝排除法检测细胞计数,甲基纤维素检测白血病菌落形成单位,免疫荧光检测PML-RARa / PML蛋白的位置。结果:抗PML起始密码子区反义(STAS)和抗PML-RARa融合区反义(FUAS)均能抑制细胞生长和急性髓细胞集落形成单元(AML-CFU)的形成。在第5天,细胞开始部分分化,在FUAS处理的细胞中比在STAS中更明显。在STAS和FUAS处理的细胞中,PML-RARa mRNA表达的下调在24小时发生,并维持长达72小时。用抗PML单克隆抗体进行的免疫荧光分析表明,微粒的减少甚至完全消失,也有明显降低。残留颗粒变得离散点状(每个细胞<10个),类似于某些经STAS处理的细胞在24小时时的正常POD结构。在72小时时,几乎所有的颗粒消失了。在FUAS处理的细胞中观察到类似的变化。结论:PML和PML-RARa反义寡核苷酸均可在mRNA和蛋白水平上特异性阻断PML-RARa的表达。 PML蛋白与细胞分化的调控有关。

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