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作 者:张翔[1] 林承杰[1] 黄新辉[1] 曾永毅[1] 刘景丰[1]
机构地区:[1]福建医科大学附属第一医院肝胆胰外科二区,福州350005
出 处:《中华实验外科杂志》2014年第8期1706-1708,共3页Chinese Journal of Experimental Surgery
基 金:福建省自然科学基金资助项目(2011J01162);福建省卫生厅青年课题(2012-2-47);福建省属高校基金资助项目(JK2011021)
摘 要:目的 观察白细胞介素(IL)-8对CD133+肝癌干细胞侵袭转移能力的影响并探讨其机制.方法 磁珠分选MHCC97-H细胞,检测上清液中IL-8表达,比较CD133+/CD133-细胞克隆形成、裸鼠成瘤、迁移侵袭能力.IL-8中和抗体处理细胞并分组,比较克隆形成、迁移侵袭能力.结果 CD133+细胞表达更高水平的IL-8[(85.76±2.55) ng/L比(13.40 ±2.19) ng/L],细胞浓度为1×106/L时即可成瘤;其克隆形成[(13.50±0.62)%比(4.43±0.31)%]、迁移[(39.3±3.2)个比(18.0±2.6)个]、侵袭[(37.5±3.0)个比(20.3±1.8)个]能力强于CD133-细胞.IL-8中和抗体处理后,CD133+/CD133-细胞的克隆形成率降低[(4.63±0.47)%比(12.93±0.55)%,(3.53±0.49)%比(6.67±0.15)%],CD133+细胞的迁移[(24.7±2.8)个比(37.7±2.8)个]、侵袭[(25.2±2.1)个比(40.2±3.6)个]能力降低,CD133-细胞无明显变化.结论 IL-8可特异性地参与调节CD133+肝癌干细胞的侵袭转移能力.Objective To study the effect and possible mechanism of interleukin (IL)-8 on migration and invasion of CD133 + liver cancer stem cells (LCSCs).Methods CD133 + cells were isolated by using magnetic-activated cell sorting (MACS) from MHCC97-H cells.Migration,invasion and colony formation efficiency of CD133 +/CD133-cells were detected.IL-8 in the supernatants was detected by enzyme linked immunosorbent assay (ELISA).Tumor-forming ability was observed by xenografts in the BALB/c nude mice.The effect of IL-8 neutalizing antibody on migration,invasion and colony formation efficiency of the sorted cells was determined.Results IL-8 was up-regulated in CD133 + cells [(85.76 ± 2.55) ng/L] as compared with CD133-cells [(13.40 ± 2.19) ng/L].The CD133 + cells exhibited a greater ability of colony formation efficiency [(13.50 ± 0.62) % vs.(4.43 ± 0.31) %],migration [(39.3 ± 3.2) vs.(18.0 ± 2.6)],invasion [(37.5 ± 3.0) vs.(20.3 ± 1.8)] and tumors initiation.Colony formation efficiency was decreased in both CD133 + [(4.63 ± 0.47)% vs.(12.93 ± 0.55)%] and CD133-[(3.53 ±0.49)% vs.(6.67 ±0.15)%] cells treated by IL-8 neutralizing antibody.IL-8 neutralizing antibody suppressed the migration [(24.7 ± 2.8) vs.(37.7 ± 2.8)] and invasion [(25.2 ± 2.1) vs.(40.2 ± 3.6)] of the CD133 + cells specifically.Conclusion CD133 plays a functional part in regulating migration and invasion of LCSCs via regulating IL-8 signaling.
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