A three-dimensional biomimetic microfluidic chip to study the behavior of hepatic stellate cell under the tumor microenvironment

被引:6
作者
Kuang, Jingjing [1 ]
Sun, Wei [1 ]
Zhang, Min [2 ]
Kang, Lu [1 ]
Yang, Shenglong [1 ]
Zhang, Hongyang [1 ]
Wang, Yuerong [1 ]
Hu, Ping [1 ]
机构
[1] East China Univ Sci & Technol, Sch Chem & Mol Engn, Shanghai Key Lab Funct Mat Chem, Shanghai 200237, Peoples R China
[2] East China Univ Sci & Technol, Engn Res Ctr Pharmaceut Proc Chem, Sch Pharm, Minist Educ, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
Interstitial flow; Hypoxia; Microfluidic; Tumor microenvironment; Behavior; MASS-TRANSPORT; SHEAR-STRESS; CANCER-CELLS; HYPOXIA; MIGRATION; CULTURE; LIVER; DIFFERENTIATION; ANGIOGENESIS; PROGRESSION;
D O I
10.1016/j.cclet.2022.05.087
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this paper, we designed a three-dimensional cell co-cultured microfluidic chip, which generated inter-stitial flow and oxygen gradient to simulate the complex tumor microenvironment. It consisted of five parallel cell culture channels and one hypoxic channel. These channels were constructed for the culture of mouse liver tumor cells (Hepa1-6), mouse liver stellate cells (JS-1), the simulation of extracellular ma-trix, complex biochemical factors (hypoxia and interstitial flow), and the supply of cellular nutrients. The 3D-interstitial flow-hypoxia model was used to study the behavior of JS-1 cells under the effect of tumor microenvironment (TME). The results showed that by co-cultured with Hepa1-6 cells, hypoxia of Hepa1-6 cells, and adding TGF-beta 1 by interstitial flow, the migration of JS-1 cells could be promoted. Similarly, activated JS-1 cells could led to the epithelial-mesenchymal transformation in co-cultured Hepa1-6 cells, which secreted more TGF-beta 1. (c) 2023 Published by Elsevier B.V. on behalf of Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences.
引用
收藏
页数:4
相关论文
共 43 条
[11]   Transforming Growth Factor β Superfamily Signaling in Development of Colorectal Cancer [J].
Jung, Barbara ;
Staudacher, Jonas J. ;
Beauchamp, Daniel .
GASTROENTEROLOGY, 2017, 152 (01) :36-52
[12]   A three-dimensional microfluidic tumor cell migration assay to screen the effect of anti-migratory drugs and interstitial flow [J].
Kalchman, Johann ;
Fujioka, Shingo ;
Chung, Seok ;
Kikkawa, Yamato ;
Mitaka, Toshihiro ;
Kamm, Roger D. ;
Tanishita, Kazuo ;
Sudo, Ryo .
MICROFLUIDICS AND NANOFLUIDICS, 2013, 14 (06) :969-981
[13]   Interstitial Flow Recapitulates Gemcitabine Chemoresistance in A 3D Microfluidic Pancreatic Ductal Adenocarcinoma Model by Induction of Multidrug Resistance Proteins [J].
Kramer, Bart ;
de Haan, Luuk ;
Vermeer, Marjolein ;
Olivier, Thomas ;
Hankemeier, Thomas ;
Vulto, Paul ;
Joore, Jos ;
Lanz, Henriette L. .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2019, 20 (18)
[14]   An artificial liver sinusoid with a microfluidic endothelial-like barrier for primary hepatocyte culture [J].
Lee, Philip J. ;
Hung, Paul J. ;
Lee, Luke P. .
BIOTECHNOLOGY AND BIOENGINEERING, 2007, 97 (05) :1340-1346
[15]  
Li DQ, 2009, TISSUE ENG PT A, V15, P2773, DOI [10.1089/ten.tea.2008.0540, 10.1089/ten.TEA.2008.0540]
[16]   Macrophage-Secreted TNFα and TGFβ1 Influence Migration Speed and Persistence of Cancer Cells in 3D Tissue Culture via Independent Pathways [J].
Li, Ran ;
Hebert, Jess D. ;
Lee, Tara A. ;
Xing, Hao ;
Boussommier-Calleja, Alexandra ;
Hynes, Richard O. ;
Lauffenburger, Douglas A. ;
Kamm, Roger D. .
CANCER RESEARCH, 2017, 77 (02) :279-290
[17]   Hypoxia: A key regulator of angiogenesis in cancer [J].
Liao, Debbie ;
Johnson, Randall S. .
CANCER AND METASTASIS REVIEWS, 2007, 26 (02) :281-290
[18]   Differentiation arrest by hypoxia [J].
Lin, Qun ;
Lee, Yi-Jang ;
Yun, Zhong .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (41) :30678-30683
[19]   Oxygen-induced cell migration and on-line monitoring biomarkers modulation of cervical cancers on a microfluidic system [J].
Lin, Xuexia ;
Chen, Qiushui ;
Liu, Wu ;
Zhang, Jie ;
Wang, Shiqi ;
Lin, Zhixiong ;
Lin, Jin-Ming .
SCIENTIFIC REPORTS, 2015, 5
[20]   A four-organ-chip for interconnected long-term co-culture of human intestine, liver, skin and kidney equivalents [J].
Maschmeyer, Ilka ;
Lorenz, Alexandra K. ;
Schimek, Katharina ;
Hasenberg, Tobias ;
Ramme, Anja P. ;
Huebner, Juliane ;
Lindner, Marcus ;
Drewell, Christopher ;
Bauer, Sophie ;
Thomas, Alexander ;
Sambo, Naomia Sisoli ;
Sonntag, Frank ;
Lauster, Roland ;
Marx, Uwe .
LAB ON A CHIP, 2015, 15 (12) :2688-2699