摘要
目的研究PBK/TOPK在HU(羟基脲)诱导白血病细胞K562的分化时的表达及意义。方法用不同浓度的羟基脲对K562细胞进行诱导分化实验,通过联苯胺、吉姆萨-瑞氏染色和流式细胞仪证实其分化方向;用Western blot法检测PBK/TOPK在K562细胞分化前后表达的变化。结果400μmol/L的羟基脲对K562作用4d后具有良好的诱导分化效果,并诱导其向红系分化,且PBK/TOPK在K562细胞向成熟分化后表达不变,而Pho-PBK/TOPK和Pho-p38有少量增加。结论HU能抑制白血病细胞K562的增殖,并诱导其向红系分化,在此过程中,有激活的PBK/TOPK参与,推测很可能通过磷酸化下游分子p38而起作用。
Objective To investigate the effect of PBK/TOPK expression during differentiation of K562 leukemia. Methods The differentiation of K562 cells was induced by Hydroxyurea(HU) in different concentrations. The differentiation models were evaluated by the staining of benzidine and Wright-Giemsa and fluorescence activivated cell analyzer(FCAS). Western blot was deteced the expression of PBK/TOPK. Results HU can induced elytroid differentiation of K562 cell line in the concentration of 400/μmol/L in 4 days. The expression of PBK/TOPK still unchanged, whereas phosphorylation PBK/TOPK and phosphorylation p38 were increased. Conclusion HU can inhibit the proliferation of K562 cells and induce the differentiation of K562 cells along the elytroid, phosphorylation PBK/TOPK expression play a role in this process by phosphorylation p38.
出处
《肿瘤防治研究》
CAS
CSCD
北大核心
2008年第2期92-94,共3页
Cancer Research on Prevention and Treatment