| Literature DB >> 31016666 |
Ruby E H Karsten1, Dorenda Oosterhuis2, Louise A van Wijk2, Peter Olinga3.
Abstract
To mimic (human) cholestasis in vitro requires multiple triggers to establish a diseased phenotype. However, this is currently not simulated by existing in vitro models. Therefore, there is a high need for multicellular systems similar to the human physiology. In such an in vitro model, cell-cell interactions and intact bile canaliculi with functional bile flow should be present and preserved during long-term culture. Precision-cut liver slices represent an ex vivo tissue culture technique that replicates most of the multicellular characteristics of a whole liver in vivo. This chapter describes the preparation and culturing of (human) precision-cut liver slices. Furthermore, a protocol to use the precision-cut liver slices technique to predict drug-induced cholestatic liver injury is described.Entities:
Keywords: ATP assay; Ex vivo model; Human bile acid mixture; Krebs Henseleit buffer; Precision-cut liver slices; Protein assay; Rat bile acid mixture; University of Wisconsin Organ preservation solution; Williams’ medium E
Mesh:
Year: 2019 PMID: 31016666 DOI: 10.1007/978-1-4939-9420-5_23
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745