Study of Viral Vectors in a Three-dimensional Liver Model Repopulated with the Human Hepatocellular Carcinoma Cell Line HepG2

被引:7
作者
Hiller, Thomas [1 ]
Roehrs, Viola [1 ]
Dehne, Eva-Maria [2 ]
Wagner, Anke [1 ,3 ]
Fechner, Henry [1 ]
Lauster, Roland [2 ]
Kurreck, Jens [1 ]
机构
[1] Berlin Univ Technol, Inst Biotechnol, Dept Appl Biochem, Berlin, Germany
[2] Berlin Univ Technol, Inst Biotechnol, Dept Med Biotechnol, Berlin, Germany
[3] Berlin Univ Technol, Inst Biotechnol, Dept Bioproc Engn, Berlin, Germany
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2016年 / 116期
关键词
Cancer Research; Issue; 116; adeno-associated virus vectors; extracellular matrix; liver; recellularization; RNA interference; short hairpin RNA; bioengineering;
D O I
10.3791/54633
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
This protocol describes the generation of a three-dimensional (3D) ex vivo liver model and its application to the study and development of viral vector systems. The model is obtained by repopulating the extracellular matrix of a decellularized rat liver with a human hepatocyte cell line. The model permits studies in a vascularized 3D cell system, replacing potentially harmful experiments with living animals. Another advantage is the humanized nature of the model, which is closer to human physiology than animal models. In this study, we demonstrate the transduction of this liver model with a viral vector derived from adeno-associated viruses (AAV vector). The perfusion circuit that supplies the 3D liver model with media provides an easy means to apply the vector. The system permits monitoring of the major metabolic parameters of the liver. For final analysis, tissue samples can be taken to determine the extent of recellularization by histological techniques. Distribution of the virus vector and expression of the delivered transgene can be analyzed by quantitative PCR (qPCR), Western blotting and immunohistochemistry. Numerous applications of the vector model in basic research and in the development of gene therapeutic applications can be envisioned, including the development of novel antiviral therapeutics, cancer research, and the study of viral vectors and their potential side effects.
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页数:6
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