›› 2012, Vol. 43 ›› Issue (4): 473-478.doi: 10.3969/j.issn.0529-1356.2012.04.007

• 细胞和分子生物学 • 上一篇    下一篇

人参皂苷Rg1诱导人白血病K562细胞复制性衰老的机制

李建平; 蔡世忠; 刘俊; 周玥; 刘典锋; 王亚平; 顾恒伟*    

  1. 1.重庆医科大学组织学胚胎学教研室; 2.干细胞与组织工程学研究室,重庆 400016
  • 收稿日期:2011-10-25 修回日期:2012-03-22 出版日期:2012-08-06
  • 通讯作者: 顾恒伟

Replicative senescence characteristics of human leukemia cell line (K562) induced by ginsenoside Rg1

  1. 1. Department of Histology and Embryology; 2.Institute of Stem Cell and Tissue Engineering, Chongqing Medical University, Chongqing 400016, China
  • Received:2011-10-25 Revised:2012-03-22 Online:2012-08-06
  • Contact: Gu Heng-wei

关键词: 人参皂苷Rg1, 白血病, K562细胞株, 复制性衰老, 衰老相关β-半乳糖苷酶染色, 四甲基偶氮唑盐法

Abstract: Objective To discuss the characteristic changes of leukemia cell line K562 on replicative senescence induced by ginsenoside Rg1. Methods The effect of Rg1 on the leukemia K562 cell line proliferation was detected by MTT colorimetric test in order to screen optimal time and drug concentration induced cells senescence. The flow cytometry method was used to analyze the cell’s cycle. The percentage of positive cells, the telomere length and the expression of the senescence -related proteins P21,P53,Rb were detected by SA-β-gal staining, southern blotting and western blotting methods, respectively. The ultrastructural senescence changes were observed under the a transmission electronic microscope. Results The optimal time and concentration in order to inhibit the proliferation of K562 cells were 48hours and 20mol/L respectively. The K562 cells arrested G2/M phase. The percentage of positive cells was increased (EM>P/EM> <0.05 ). The senescence -related proteins were up-regulated (EM>P/EM> <0.05). The telomere length became shorten quickly ( EM>P/EM> <0.05 ). Conclusion Rg1 may induce leukemia cell line K562 into the state of replicative senescence by the ce

Key words: Ginsenoside Rg1, Leukemia, K562 cell line, Replicative senescence, SA-β-Gal staining, MTT, Human

中图分类号: