Sharif-Khatibi Leila, Kariminia Amina, Khoei Sameide, Goliaei Bahram
Institute of Biochemistry and Biophysics, University of Tehran, Tehran, Iran.
Int J Hyperthermia. 2007 Dec;23(8):645-55. doi: 10.1080/02656730701769833.
The aim of the present study was to investigate whether induction of differentiation by hyperthermia is accompanied by apoptosis and necrosis to further evaluate the benefits of using hyperthermia as a differentiation inducing physical modality.
Differentiation was evaluated in K562 erythroleukaemia cells by measuring haemoglobin synthesis and flow cytometric measurement of glycophorin A expression. Apoptosis was measured by Annexin-V-FITC and Propidium Iodide (PI) double staining assay. Apoptosis and necrosis was also evaluated morphologically using staining with acridine orange/ethidium bromide (AO/EtBr) by fluorescence microscopy. Heat shock protein 70 (HSP70) level was measured by ELISA kit.
Hyperthermia (43 degrees C) induced differentiation as judged by increased haemoglobin synthesis and glycophorin A expression. No sign of apoptosis or necrosis could be detected at this temperature. Cell viability did not change due to heat treatment, and cellular proliferation was reduced in a dose (heating time) dependent manner. At 45 degrees C, hyperthermia induced apoptosis and necrosis with minimal or no sign of differentiation. HSP70 level was significantly increased at 43 degrees C along with differentiation of leukaemic cells, while at 45 degrees C no significant effect on HSP70 production could be observed.
The encouraging results obtained here indicate that by heat treatment at 43 degrees C, hyperthermia can be used alone or in combination with other modalities as a differentiation inducing agent without any detectable apoptotic activity. Positive correlation between HSP70 production and induction of differentiation and lack of apoptosis by hyperthermia confirm the possible role of HSP70 in the heat-induced differentiation and apoptosis in leukaemic cells.
本研究旨在探究热疗诱导分化是否伴随着凋亡和坏死,以进一步评估将热疗作为一种诱导分化的物理方式的益处。
通过测量血红蛋白合成以及用流式细胞术检测血型糖蛋白A的表达,来评估K562红白血病细胞的分化情况。采用膜联蛋白-V-异硫氰酸荧光素(Annexin-V-FITC)和碘化丙啶(PI)双染法检测凋亡。还用吖啶橙/溴化乙锭(AO/EtBr)染色,通过荧光显微镜从形态学上评估凋亡和坏死情况。使用酶联免疫吸附测定试剂盒测量热休克蛋白70(HSP70)水平。
热疗(43℃)通过血红蛋白合成增加和血型糖蛋白A表达上调诱导了分化。在此温度下未检测到凋亡或坏死迹象。热处理后细胞活力未改变,且细胞增殖以剂量(加热时间)依赖的方式降低。在45℃时,热疗诱导了凋亡和坏死,分化迹象极少或没有。在43℃时,随着白血病细胞的分化,HSP70水平显著升高,而在45℃时,未观察到对HSP70产生有显著影响。
此处获得的令人鼓舞的结果表明,通过43℃的热处理,热疗可单独使用或与其他方式联合作为一种诱导分化剂,且无任何可检测到的凋亡活性。HSP70产生与分化诱导之间的正相关以及热疗无凋亡现象,证实了HSP70在白血病细胞热诱导分化和凋亡中可能发挥的作用。