首页> 外文期刊>Journal of Huazhong University of Science and Technology >Expression and Fuactional Role of HERG1, K~+ Channels in Leukemic Cells and Leukemic Stem Cells
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Expression and Fuactional Role of HERG1, K~+ Channels in Leukemic Cells and Leukemic Stem Cells

机译:HERG1,K〜+通道在白血病细胞和白血病干细胞中的表达及其功能

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摘要

In order to investigate the expression and functional role of HERG1 K~+ channels in leukemic cells and leukemic stem cells (LSCs), RT-PCR was used to detect the HERG1 K~+ channels expression in leukemic cells and LSCs. The functional role of HERG1 K~+ channels in leukemic cell proliferation was measured by MTT assay, and cell cycle and apoptosis were analyzed by flow cy-tometry. The results showed that herg mRNA was expressed in CD34~+/CD38, CD123~+ LSCs but not in circulating CD34~+ cells. Herg mRNA was also up-regulated in leukemia cell lines K562 and HL60 as well as almost all the primary leukemic cells while not in normal peripheral blood mononuclear cells (PBMNCs) and the expression of herg mRNA was not associated with the clinical and cytogenetic features of leukemia. In addition, leukemic cell proliferation was dramatically inhibited by HERG K~+ channel special inhibitor E-4031. Moreover, E-4031 suppressed the cell growth by inducing a specific block at the G1/S transition phase of the cell cycle but had no effect on apoptosis in leukemic cells. The results suggested that HERG1 K~+ channels could regulate leukemic cells proliferation and were necessary for leukemic cells to proceed with the cell cycle. HERG1 K~+ channels may also have oncogenic potential and may be a biomarker for diagnosis of leukemia and a novel potential pharmacological target for leukemia therapy.
机译:为了研究HERG1 K〜+通道在白血病细胞和白血病干细胞(LSCs)中的表达及其功能作用,采用RT-PCR技术检测HERG1K〜+通道在白血病细胞和LSCs中的表达。 MTT法检测HERG1 K〜+通道在白血病细胞增殖中的功能,流式细胞术分析其细胞周期和凋亡。结果表明herg mRNA在CD34〜+ / CD38,CD123〜+ LSCs中表达,而在循环CD34〜+细胞中不表达。 Herg mRNA在白血病细胞株K562和HL60以及几乎所有原发性白血病细胞中也上调,而在正常外周血单核细胞(PBMNCs)中则不表达,而且herg mRNA的表达与白血病的临床和细胞遗传学特征无关。白血病。另外,HERG K〜+通道特异性抑制剂E-4031可显着抑制白血病细胞的增殖。此外,E-4031通过在细胞周期的G1 / S过渡阶段诱导特异性阻断来抑制细胞生长,但对白血病细胞的凋亡没有影响。结果表明,HERG1 K〜+通道可调节白血病细胞的增殖,是白血病细胞继续细胞周期的必要条件。 HERG1 K〜+通道也可能具有致癌作用,可能是诊断白血病的生物标志物,也是治疗白血病的新药理学靶标。

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