巨噬细胞集落刺激因子对肺癌细胞株A549在体外的抑制作用

彭胜祖; 闵家新; 蒋力

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巨噬细胞集落刺激因子对肺癌细胞株A549在体外的抑制作用

论著 | 更新时间：2026-01-09

- 巨噬细胞集落刺激因子对肺癌细胞株A549在体外的抑制作用
- Inhibitory effect of macrophage colony stimulating factor on lung cancer cell line A549
- 陆军军医大学学报 2007年29卷第5期页码：419-421
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  中图分类号： R329.1;R734.2;R730.2
- 纸质出版：2007
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彭胜祖,闵家新,蒋力.巨噬细胞集落刺激因子对肺癌细胞株A549在体外的抑制作用[J].陆军军医大学学报(原第三军医大学学报),2007,29(05):419-421.

　PENG Sheng-zu,MIN Jia-xin,JIANG Li.Inhibitory effect of macrophage colony stimulating factor on lung cancer cell line A549[J].J Amry Med Univ (J Third Mil Med Univ),2007,29(05):419-421.
彭胜祖,闵家新,蒋力.巨噬细胞集落刺激因子对肺癌细胞株A549在体外的抑制作用[J].陆军军医大学学报(原第三军医大学学报),2007,29(05):419-421. DOI：

　PENG Sheng-zu,MIN Jia-xin,JIANG Li.Inhibitory effect of macrophage colony stimulating factor on lung cancer cell line A549[J].J Amry Med Univ (J Third Mil Med Univ),2007,29(05):419-421. DOI：

摘要

目的观察巨噬细胞集落刺激因子（macrophage colony stimulating factor

M-CSF）对肺腺癌细胞株A549的作用。方法观察肺腺癌A549细胞形态的变化。M-CSF对体外培养肺腺癌A549细胞的生长抑制作用采用MTT 检测法

用流式细胞仪检测细胞DNA含量

分析M-CSF对细胞周期的影响。采用RT-PCR检测M-CSF受体mRNA表达的变化。结果 M-CSF能显著抑制肺腺癌A549细胞的生长，并且呈浓度、时间依赖关系，在M-CSF浓度为10 ng/ml时有最大抑制效应。流式细胞仪检测分析显示M-CSF作用后G

期细胞增加。RT-PCR显示经M-CSF作用后M-CSF受体的mRNA表达水平有所下降。结论 M-CSF对肺癌细胞株A549在体外有抑制作用。

Abstract

Objective To explore the effect of macrophage colony stimulating factor (M-CSF) on lung cancer cell line A549. Methods After M-CSF at 0.1

1 and 10 ng/ml was given to cultured A549 cells for 0

72 and 92 h respectively

their morphological changes were observed with inverted microscopy

proliferation was measured by MTT assay

and cell cycles were determined by flow cytometry. RT-PCR was used to detect the change of expression of M-CSF receptor. Result The growth of A549 was significantly inhibited by M-CSF in a concentration- and time- dependent manner. The maximum response was obtained at 10 ng/ml of M-CSF. Flow cytometric analysis revealed that the t

reated A549 cells arrested at the G

phase of the cell cycle. RT-PCR showed that the mRNA expression of M-CSF receptor was reduced after the M-CSF treatment. Conclusion M-CSF has an anti-tumour activity on lung cancer cell A549.

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