Baśkiewicz-Masiuk Magdalena, Machaliński Bogusław
Department of General Pathology, Pomeranian Medical University, Szczecin, Poland.
Eur J Haematol. 2004 Jun;72(6):420-9. doi: 10.1111/j.1600-0609.2004.00242.x.
The STAT5 proteins are activated by many haematological cytokines and growth factors. They regulate cell cycle, apoptosis and proliferation of different cells via the influence on gene transcription. Because STAT5s are constitutively activated in certain haematooncologic diseases, they are suggested to play an important role in leukaemogenesis. However, the real function of these proteins in haematopoietic cell transformation and proliferation is not clear enough. The aim of this study was to evaluate the influence of suppression of STAT5A and STAT5B expression on the clonogenicity and apoptosis of the chronic myeloid leukaemia (CML) and acute myeloid leukaemia (AML) cells.
Blast cells from 34 newly diagnosed patients with CML and AML were used in our experiments. Antisense oligodeoxynucleotides (ODNs) were applied to block STAT5A and STAT5B at the mRNA level and the RT-PCR method was used to study STAT5 mRNA expression in the cells after incubation with ODNs. Moreover, Western blot analysis of the STAT5 proteins was performed. The effect of ODN pretreatment on cell clonogenicity in methylocellulose cultures was examined according to the type of oligodeoxynucleotide and the time of exposure. The induction of apoptosis in cells was also estimated by the Annexin V/PI staining and the TUNEL method using flow cytometry.
Perturbation of STAT5 expression decreased proliferative potential of the CML and the AML blasts as well as enhanced their apoptosis (P < 0.05).
Our studies showed that the STAT5 proteins may be critical in the regulation of growth and apoptosis of the CML and AML leukaemic cells.
信号转导和转录激活因子5(STAT5)蛋白可被多种血液学细胞因子和生长因子激活。它们通过影响基因转录来调节不同细胞的细胞周期、凋亡和增殖。由于STAT5在某些血液肿瘤疾病中持续激活,因此提示其在白血病发生过程中发挥重要作用。然而,这些蛋白在造血细胞转化和增殖中的实际功能尚不清楚。本研究旨在评估抑制STAT5A和STAT5B表达对慢性髓性白血病(CML)和急性髓性白血病(AML)细胞克隆形成能力和凋亡的影响。
我们的实验使用了34例新诊断的CML和AML患者的原始细胞。应用反义寡脱氧核苷酸(ODN)在mRNA水平阻断STAT5A和STAT5B,并采用逆转录-聚合酶链反应(RT-PCR)方法研究与ODN孵育后细胞中STAT5 mRNA的表达。此外,还进行了STAT5蛋白的蛋白质印迹分析。根据寡脱氧核苷酸的类型和暴露时间,检测ODN预处理对甲基纤维素培养物中细胞克隆形成能力的影响。还通过膜联蛋白V/碘化丙啶(Annexin V/PI)染色和使用流式细胞术的末端脱氧核苷酸转移酶介导的缺口末端标记(TUNEL)法评估细胞凋亡的诱导情况。
STAT5表达的扰动降低了CML和AML原始细胞的增殖潜能,并增强了它们的凋亡(P < 0.05)。
我们的研究表明,STAT5蛋白可能在CML和AML白血病细胞的生长和凋亡调节中起关键作用。