Interaction study of cancer cells and fibroblasts on a spatially confined oxygen gradient microfluidic chip to investigate the tumor microenvironment

被引:20
|
作者
Sun, Wei [1 ]
Chen, Yuqing [1 ]
Wang, Yuerong [1 ]
Luo, Pei [2 ]
Zhang, Min [3 ,4 ]
Zhang, Hongyang [1 ]
Hu, Ping [1 ]
机构
[1] East China Univ Sci & Technol, Shanghai Key Lab Funct Mat Chem, Sch Chem & Mol Engn, Shanghai 200237, Peoples R China
[2] Macau Univ Sci & Technol, State Key Lab Qual Res Chinese Med, Macau Inst Appl Res Med & Hlth, Taipa, Macau, Peoples R China
[3] East China Univ Sci & Technol, Shanghai Key Lab New Drug Design, Sch Pharm, Shanghai 200237, Peoples R China
[4] East China Univ Sci & Technol, Modern Engn Ctr TCM, Sch Pharm, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
HYPOXIA; CULTURE; CYTOTOXICITY; PROGRESSION; RESISTANCE; MIGRATION; INVASION;
D O I
10.1039/c8an01216d
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This paper reports a single-layered microfluidic device for studying the interaction of cancer cells and fibroblasts in an oxygen gradient. This gradient can be established from 1.9% to 18.8% using a spatially confined oxygen scavenging chemical reaction. Due to the spatial design of the chip, only cancer cells can sustain low oxygen conditions when co-cultured with fibroblasts in the adjacent channels, simulating the cell-cell interactions of the hypoxic cancer cells and the surrounding fibroblasts in tumor microenvironment in vivo. Moreover, a cell migration assay is performed on the chip for studying the tumor invasion ability. The results show that the migration speed of B16 cells is increased by hypoxia and the co-culture with L929 cells. In addition, we use ELISA to quantify the migration-related cytokines transforming growth factor-beta 1 (TGF-beta 1) in the microfluidic system. Our results confirm interaction between cancer cells and fibroblasts. This microfluidic device provides new insight for the investigation of tumor microenvironment and cell interactions.
引用
收藏
页码:5431 / 5437
页数:7
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