基础医学与临床 ›› 2013, Vol. 33 ›› Issue (9): 1112-1117.

• 研究论文 • 上一篇    下一篇

骨髓间充质干细胞在肺腺癌微环境中的遗传稳定性及增殖能力

秦洁1,李屹2,刘永琦1,王倩1,舍雅莉1,骆亚莉1   

  1. 1. 甘肃中医学院
    2. 兰州大学
  • 收稿日期:2012-09-25 修回日期:2012-12-07 出版日期:2013-09-05 发布日期:2013-08-28
  • 通讯作者: 刘永琦 E-mail:liuyongqi73@sina.com
  • 基金资助:
    国家自然科学基金项目;甘肃省教育厅科研基金项目

Genetic stability and proliferation capacity of human bone marrow mesenchymal stem cells in pulmonary adenocarcinoma microenvironment

  • Received:2012-09-25 Revised:2012-12-07 Online:2013-09-05 Published:2013-08-28

摘要: 目的 探讨人骨髓间充质干细胞(HMSC-bm)在肺腺癌微环境中遗传稳定性的变化。 方法 通过6孔板结合Transwell小室建立HMSC-bm和A549细胞的共培养体系,倒置相差显微镜下观察细胞的形态; MTT法检测细胞的增殖能力;常规染色体及G显带核型分析细胞的染色体;Western blot检测组蛋白去乙酰化酶4(HDAC4)的表达。以单独培养的HMSC-bm,A549作为对照组。结果 共培养组细胞胞核大而深染,可见病理性核分裂象, HMSC-bm组无明显变化;细胞增殖曲线呈S型,共培养组细胞于第4天开始增殖速率快于HMSC-bm组;共培养组染色体数目为亚三倍体、三倍体,有明显的染色体异常;共培养组细胞HDAC4表达明显高于HMSC-bm组(p<0.01)。结论 肺腺癌微环境可改变HMSC-bm的增殖速率和其遗传稳定性。

关键词: HMSC-bm, 肺腺癌微环境, 遗传稳定性, 染色体

Abstract: Objective To investigate the genetic stability of human bone marrow mesenchymal stem cells (HMSC-bm) under pulmonary adenocarcinoma microenvironment. Methods A co-cultured system of HMSC-bm and A549 cells was established through the combination of 6 well culture plate and transwell chamber as experimental group while HMSC-bm and A549 cells were cultured separately as the control groups. The morphology of the cells was observed by phase-contrast microscopy. The proliferation curve of mesenchymal stem cells was tested by MTT. Chromosome was examined by karyotyping analysis. The expression of HDAC4 protein was detected by Western blot. Results Cells in the co-culture group showed that the cell nucleus became bigger than the nucleus in HMSC-bm group and exhibited anachromasis in 7 days. The proliferation curve indicated faster proliferation of co-cultured HMSC-bm than HMSC-bm. Karyotyping analysis showed that the chromosome number of co-cultured HMSC-bm was hypotriploid and triploid and the chromosome was grossly abnormal. The expression of HDAC4 protein in co-cultured HMSC-bm significantly increased compared to that in HMSC-bm (p<0.01). Conclusion Pulmonary adenocarcinoma microenvironment could influence the proliferation speed and the genetic stability of HMSC-bm .

Key words: HMSC-bm, pulmonary adenocarcinoma microenvironment, genetic stability, chromosome