基础医学与临床 ›› 2016, Vol. 36 ›› Issue (2): 179-185.

• 研究论文 • 上一篇    下一篇

衰老调控因子SIRT6在人参皂苷Rg1延缓造血干/祖细胞衰老中的作用

周玥1,王亚平2,王建伟2,丁继超1   

  1. 1. 云南省大理学院基础医学院组
    2. 重庆医科大学
  • 收稿日期:2015-02-11 修回日期:2015-05-24 出版日期:2016-02-05 发布日期:2016-01-21
  • 通讯作者: 周玥 E-mail:zhouyue_120@sina.com
  • 基金资助:
    衰老调控因子SIRT6与NF-κB对话在人参皂苷Rg1延缓造血干/祖细胞衰老中的作用;国家自然科学基金资助项目

The effect of SIRT6 on delaying hematopoietic stem cell and progenitor cell senescence with ginsenoside Rg1

  • Received:2015-02-11 Revised:2015-05-24 Online:2016-02-05 Published:2016-01-21

摘要: 目的 探讨SIRT6在人参皂苷Rg1延缓造血干/祖细胞(HSC/HPC)衰老中的作用。方法 三丁基过氧化氢(t-BHP)诱导Sca-1+HSC/HPC衰老,构建HSC/HPC衰老体外模型,Sca-1+HSC/HPC连续移植3代,构建HSC/HPC衰老体内模型。给予体内外衰老模型Rg1预防和治疗衰老处理。造血祖细胞混合集落(CFU-Mix)培养,细胞周期分析和衰老相关β-半乳糖苷酶(SA-β-Gal)染色,分析Rg1体内外调控Sca-1+HSC/HPC衰老的作用。荧光定量PCR及Western blot检测衰老调控因子SIRT6 mRNA及蛋白的表达。结果 与体内外衰老模型组相比,Rg1治疗及预防衰老处理后Sca-1+HSC/HPC G0/G1期细胞比例、SA-β-Gal染色阳性率下降(P<0.05),CFU-Mix数量升高(P<0.05);SIRT6 mRNA及蛋白表达上调(P<0.05);Rg1预防衰老组各指标变化均较Rg1治疗衰老组明显。结论 Rg1在体内外均可通过调控SIRT6 发挥其延缓Sca-1+HSC/HPC衰老的作用。

关键词: SIRT6, Sca-1+HSC/HPC, 衰老, 人参皂苷Rg1

Abstract: Objective To investigate the effect of SIRT6 on delaying hematopoietic stem cell and progenitor cell senescence with ginsenoside Rg1. Methods HSC/HPC aged model in vitro was established by t-BHP to induce Sca-1+ HSC/HPC senescence. HSC/HPC aged model in vivo was established as well through the Sca-1+HSC/HPC serial transplantation. The effect of Rg1 to delay Sca-1+HSC/HPC senencence in vitro as well as in vivo were evaluated by senescence-associated β-galactosidase (SA-β-gal) staining, mixed hematopoietic progenitor cell culture(CFU-Mix) and cell cycle assay. The expressions of SIRT6 mRNA and protein were detected by quantitative PCR and Western blotting. Results Compared with aged model in vitro and in vivo, the number of cells entered G0/G1 phase and the percentage of SA-β-gal positive cells were decreased, the number of CFU-Mix was increased in Rg1 treated group and Rg1 prevented group. The expression of SIRT6 mRNA and protein were up regulated in Rg1 treated group and Rg1 prevented group, compared with aged model. The changes of Rg1 prevented group was significantly higher than Rg1 treated group. Conclusion Rg1 could delay Sca-1+HSC/HPC senescence in vitro and in vivo via regulating the expression of SIRT6.

Key words: SIRT6, Sca-1+ HSC/HPC, senescence, ginsenoside Rg1