Chinese Journal of Tissue Engineering Research ›› 2010, Vol. 14 ›› Issue (15): 2769-2772.doi: 10.3969/j.issn.1673-8225.2010.15.026

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Interaction between lung fibroblast and lung cancer GLC-82 cells in a three-dimensional collagen culture model

Yan Jiang-tao 1,2, Zhu Yun-Kui2, Li Ji-Dong2, Ma Guo-cheng2, Wang Shu2, Wang Xiao-Qin2   

  1. 1 Second Clinical Medical College, Lanzhou University, Lanzhou   730000, Gansu Province, China; 2 Department of Respiratory Medicine, Lanzhou General Hospital of Lanzhou Military Area Command of Chinese PLA, Lanzhou 730050, Gansu Province, China
  • Online:2010-04-09 Published:2010-04-09
  • Contact: Zhu Yun-kui, Master, Chief physician, Department of Respiratory Medicine, Lanzhou General Hospital of Lanzhou Military Area Command of Chinese PLA, Lanzhou 730050, Gansu Province, China yunkuizhu@yahoo.com.cn
  • About author:Yan Jiang-tao★, Studying for master’s degree, Physician, Second Clinical Medical College, Lanzhou University, Lanzhou 730000, Gansu Province, China; Department of Respiratory Medicine, Lanzhou General Hospital of Lanzhou Military Area Command of Chinese PLA, Lanzhou 730050, Gansu Province, China yanjt07@lzu.cn
  • Supported by:

    the Natural Science Foundation of Gansu Province, No. SZS051-A25-088*

Abstract:

BACKGROUND: The histocyte and inflammatory cells played an important role in the invasion and metastasis of lung cancer cells. However, cell interaction influenced matrix metalloproteinase.
OBJECTIVE: To observe the influence of interaction between fetal lung fibroblasts (HFL) and lung cancer cells on matrix metalloproteinase-1, 2, and 9 (MMP-1, 2, 9) expression in three-dimensional co-culture.
METHODS: Human lung cancer cells (GLC-82) and HFL were co-cultivated in three-dimensional collagen gels, which were mixed with collagen, 4 time volume DMEM and sterilizing water, as well as 1 time volume DMEM. The final concentration of collagen was 0.75 g/mL. GLC-82 and HFL were cultured individually, and GLC-82 and HFL were then co-cultured according to the ratio of 5:1. After 48 hours, the supernatant was harvested following adding 1 time volume DMEM. MMP-1 expression was detected by Western blot and MMP-2 and 9 expressions were detected by gelatin zymography.
RESULTS AND CONCLUSION: In three-dimensional co-culture of GLC-82 with HFL, the expressions of MMP-1, MMP-2 and MMP-9 were much higher than that in GLC-82 or in HFL alone (P < 0.05). This suggested that the interaction between HFL and lung cancer cells enhanced the invasion and metastasis of lung cancer through up-regulating the secretion and activation of MMP-1, MMP-2, and MMP-9. 

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