Best Practices and Progress in Precision-Cut Liver Slice Cultures

被引:37
|
作者
Dewyse, Liza [1 ]
Reynaert, Hendrik [2 ]
van Grunsven, Leo A. [1 ]
机构
[1] Vrije Univ Brussel, Dept Basic Biomed Sci, Liver Cell Biol Res Grp, B-1090 Brussels, Belgium
[2] Univ Ziekenhuis Brussel, Dept Gastroenterol & Hepatol, B-1090 Brussels, Belgium
关键词
PCLS; chronic liver disease; 3D; in vitro liver; ANTI-FIBROTIC DRUGS; IN-VITRO MODEL; RAT-LIVER; GENE-EXPRESSION; PROLONGED INCUBATION; HEPATIC STEATOSIS; KIDNEY SLICES; PPAR-GAMMA; TISSUE; CELLS;
D O I
10.3390/ijms22137137
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Thirty-five years ago, precision-cut liver slices (PCLS) were described as a promising tool and were expected to become the standard in vitro model to study liver disease as they tick off all characteristics of a good in vitro model. In contrast to most in vitro models, PCLS retain the complex 3D liver structures found in vivo, including cell-cell and cell-matrix interactions, and therefore should constitute the most reliable tool to model and to investigate pathways underlying chronic liver disease in vitro. Nevertheless, the biggest disadvantage of the model is the initiation of a procedure-induced fibrotic response. In this review, we describe the parameters and potential of PCLS cultures and discuss whether the initially described limitations and pitfalls have been overcome. We summarize the latest advances in PCLS research and critically evaluate PCLS use and progress since its invention in 1985.
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页数:18
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