Starokozhko Viktoriia, Abza Getahun B, Maessen Hedy C, Merema Marjolijn T, Kuper Frieke, Groothuis Geny M M
Division of Pharmacokinetics, Toxicology and Targeting, Groningen Research Institute for Pharmacy, University of Groningen, Antonius Deusinglaan 1, 9713 AV Groningen, The Netherlands.
TNO, Utrechtseweg 48, 3704 HE Zeist, The Netherlands.
Toxicol In Vitro. 2015 Dec 25;30(1 Pt B):288-99. doi: 10.1016/j.tiv.2015.10.008. Epub 2015 Oct 26.
Precision-cut liver slices (PCLS) are an ex vivo model for metabolism and toxicity studies. However, data on the maintenance of the morphological integrity of the various cell types in the slices during prolonged incubation are lacking. Therefore, our aims were to characterize morphological and functional changes in rat PCLS during five days of incubation in a rich medium, RegeneMed®, and a standard medium, Williams' Medium E. Although cells of all types in the slices remain viable, profound changes in morphology were observed, which were more prominent in RegeneMed®. Slices underwent notable fibrosis, bile duct proliferation and fat deposition. Slice thickness increased, resulting in necrotic areas, while slice diameter decreased, possibly indicating cell migration. An increased proliferation of parenchymal and non-parenchymal cells (NPCs) was observed. Glycogen, albumin and Cyp3a1 were maintained albeit to a different level in two media. In conclusion, both hepatocytes and NPCs remain viable and functional, enabling five-day toxicity studies. Tissue remodeling and formation of a new capsule-like cell lining around the slices are evident after 3–4 days. The differences in effects between media emphasize the importance of media selection and of the recognition of morphological changes in PCLS, when interpreting results from toxicological or pharmacological studies.
精密肝切片(PCLS)是用于代谢和毒性研究的离体模型。然而,目前缺乏关于切片在长时间孵育过程中各种细胞类型形态完整性维持情况的数据。因此,我们的目的是表征大鼠PCLS在富含营养成分的RegeneMed®培养基和标准培养基Williams' Medium E中孵育五天期间的形态和功能变化。尽管切片中所有类型的细胞均保持存活,但仍观察到明显的形态变化,这些变化在RegeneMed®培养基中更为显著。切片出现了明显的纤维化、胆管增生和脂肪沉积。切片厚度增加,导致出现坏死区域,而切片直径减小,这可能表明细胞发生了迁移。观察到实质细胞和非实质细胞(NPC)的增殖增加。在两种培养基中,糖原、白蛋白和Cyp3a1均得以维持,尽管维持水平有所不同。总之,肝细胞和NPC均保持存活且功能正常,从而能够进行为期五天的毒性研究。3 - 4天后,切片周围明显出现组织重塑并形成新的囊状细胞内衬。在解释毒理学或药理学研究结果时,两种培养基效应的差异凸显了培养基选择以及认识PCLS形态变化的重要性。