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高转移肺癌细胞株的建立及其肿瘤干细胞生物学特性

Establishment of Human Lung Adenocarcinoma Cell Line A549 with High Metastasis and Biological Characteristics of Its Cancer Stem Cells

  • 摘要:
    目的  研究高转移肺腺癌细胞株的肿瘤干细胞生物学特征。
    方法 肺腺癌细胞系A549接种裸鼠皮下成瘤后,取肺的转移灶,通过机械分离法获取肺转移细胞,体外扩大培养后,再次接种裸鼠。如此反复接种裸鼠,获得稳定肺转移的细胞株A549-V13。采用无血清悬浮培养及PKH26染色确定A549-V13存在肿瘤干细胞。流式细胞术(FACS)检测和分选A549和A549-V13中肿瘤干细胞标志物CD133的表达并进行体内外生物学特征实验。
    结果 建立稳定高转移A549-V13细胞株。无血清悬浮培养A549-V13,7天后形成的球形细胞团中存在单个PKH26阳性细胞。FACS检测显示,与A549中CD133+细胞相比,高转移A549-V13细胞株中CD133+细胞的表达比例显著提高4.85倍。A549-V13中CD133+细胞具有更强的自我更新能力,侵袭能力提高1.42倍,耐药能力也显著增强,其IC50提高1.26倍,A549-V13的CD133+细胞在裸鼠皮下接种2×102个细胞3月致瘤4/6,而接种2×102个A549的CD133+细胞3月才致瘤2/6。
    结论 建立高转移肺癌细胞株A549-V13,伴随CD133+细胞表达比例的增加,其体内外生物学功能显著增强。

     

    Abstract:
    Objective To investigate the biological characteristics of cancer stem cells derived from human lung adenocarcinoma cell line A549 with high metastasis.
    Methods A549 cells were inoculated into subcutaneous tumor. The lung metastasis cells were obtained by mechanical separation method, and then inoculated into nude mice, repeated inoculation of nude mice to obtain a stable lung metastasis of the cell line A549-V13. Serum-free spheroid formation and PKH26 staining were used to determine whether there were cancer stem cells in A549-V13 cell line. Flow cytometry was performed to detect cancer stem cell marker CD133 expression in A549 and A549-V13 cells; CD133+ expressions were sorted to identify its biological characteristics in vivo and in vitro.
    Results The high metastatic cell line A549-V13 are obtained. The single PKH26 positive cell was observed in spheroid cells after A549-V13 cells were cultured for 7 days. Compared with A549 cells, the proportion of cancer stem cell marker CD133 was significantly increased by 4.85 times in A549-V13 cells. The sorted CD133+ cells of A549-V13 showed higher self-renewal ability, resistance ability invasion ability was enhanced by 1.42 times and the IC50 was increased by 1.26 times. Nude mice inoculated with 2×102 CD133+ cells of A549-V13 developed tumor after 3 months(4/6), whereas at least 2×102 CD133+ cells A549 formed tumor for 3 months(2/6).
    Conclusion The high metastatic cell line A549-V13 are obtained. With the increase of the proportion of CD133+ cells, the biological function of CD133+ cells was significantly enhanced in vivo and in vitro.

     

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