Well plate-based perfusion culture device for tissue and tumor microenvironment replication

被引:12
作者
Zhang, W. [1 ]
Gu, Y. [1 ]
Hao, Y. [1 ]
Sun, Q. [1 ]
Konior, K. [1 ]
Wang, H. [2 ]
Zilberberg, J. [3 ,4 ]
Lee, W. Y. [1 ]
机构
[1] Stevens Inst Technol, Dept Chem Engn & Mat Sci, Hoboken, NJ 07030 USA
[2] Stevens Inst Technol, Dept Chem Chem Biol & Biomed Engn, Hoboken, NJ 07030 USA
[3] Hackensack Univ, Med Ctr, Res Dept, Hackensack, NJ 07601 USA
[4] Hackensack Univ, Med Ctr, John Theurer Canc Ctr, Hackensack, NJ 07601 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
VERSUS-HOST-DISEASE; GENE-EXPRESSION; CELL-LINES; IMPRINT LITHOGRAPHY; OSTEOCYTE; GROWTH; MODEL; BETA;
D O I
10.1039/c5lc00341e
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
There are significant challenges in developing in vitro human tissue and tumor models that can be used to support new drug development and evaluate personalized therapeutics. The challenges include: (1) working with primary cells which are often difficult to maintain ex vivo, (2) mimicking native microenvironments from which primary cells are harvested, and (3) the lack of culture devices that can support these microenvironments to evaluate drug responses in a high-throughput manner. Here we report a versatile well plate-based perfusion culture device that was designed, fabricated and used to: (1) ascertain the role of perfusion in facilitating the expansion of human multiple myeloma cells and evaluate drug response of the cells, (2) preserve the physiological phenotype of primary murine osteocytes by reconstructing the 3D cellular network of osteocytes, and (3) circulate primary murine T cells through a layer of primary murine intestine epithelial cells to recapitulate the interaction of the immune cells with the epithelial cells. Through these diverse case studies, we demonstrate the device's design features to support: (1) the convenient and spatiotemporal placement of cells and biomaterials into the culture wells of the device; (2) the replication of tissues and tumor microenvironments using perfusion, stromal cells, and/or biomaterials; (3) the circulation of non-adherent cells through the culture chambers; and (4) conventional tissue and cell characterization by plate reading, histology, and flow cytometry. Future challenges are identified and discussed from the perspective of manufacturing the device and making its operation for routine and wide use.
引用
收藏
页码:2854 / 2863
页数:10
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