Tissue Engineering of a Human 3D in vitro Tumor Test System

被引:30
作者
Moll, Corinna [1 ]
Reboredo, Jenny [1 ]
Schwarz, Thomas [1 ]
Appelt, Antje [1 ]
Schuerlein, Sebastian [1 ]
Walles, Heike [1 ]
Nietzer, Sarah [1 ]
机构
[1] Univ Hosp Wurzburg, Dept Tissue Engn & Regenerat Med, Wurzburg, Germany
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2013年 / 78期
关键词
Cancer Biology; Issue; 78; Biomedical Engineering; Bioengineering; Medicine; Anatomy; Physiology; Molecular Biology; Cellular Biology; Tissue Engineering; Tumor Cells; Cultured; Biotechnology; Culture Techniques; Cell Engineering; Cellular Microenvironment; Equipment and Supplies; Decellularization; BioVaSc; primary cell isolation; tumor test system; dynamic culture conditions; bioreactor; 3D in vitro models; cell culture; BIOREACTORS; MATRIX; CANCER;
D O I
10.3791/50460
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cancer is one of the leading causes of death worldwide. Current therapeutic strategies are predominantly developed in 2D culture systems, which inadequately reflect physiological conditions in vivo. Biological 3D matrices provide cells an environment in which cells can self-organize, allowing the study of tissue organization and cell differentiation. Such scaffolds can be seeded with a mixture of different cell types to study direct 3D cell-cell-interactions. To mimic the 3D complexity of cancer tumors, our group has developed a 3D in vitro tumor test system. Our 3D tissue test system models the in vivo situation of malignant peripheral nerve sheath tumors (MPNSTs), which we established with our decellularized porcine jejunal segment derived biological vascularized scaffold (BioVaSc). In our model, we reseeded a modified BioVaSc matrix with primary fibroblasts, microvascular endothelial cells (mvECs) and the S462 tumor cell line. For static culture, the vascular structure of the BioVaSc is removed and the remaining scaffold is cut open on one side (Small Intestinal Submucosa SIS-Muc). The resulting matrix is then fixed between two metal rings (cell crowns). Another option is to culture the cell-seeded SIS-Muc in a flow bioreactor system that exposes the cells to shear stress. Here, the bioreactor is connected to a peristaltic pump in a self-constructed incubator. A computer regulates the arterial oxygen and nutrient supply via parameters such as blood pressure, temperature, and flow rate. This setup allows for a dynamic culture with either pressure-regulated pulsatile or constant flow. In this study, we could successfully establish both a static and dynamic 3D culture system for MPNSTs. The ability to model cancer tumors in a more natural 3D environment will enable the discovery, testing, and validation of future pharmaceuticals in a human-like model.
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页数:6
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