HYPOTHERMIC STORAGE OF PIG HEPATOCYTES - INFLUENCE OF DIFFERENT STORAGE SOLUTIONS AND CELL-DENSITY

Citation
Sa. Pahernik et al., HYPOTHERMIC STORAGE OF PIG HEPATOCYTES - INFLUENCE OF DIFFERENT STORAGE SOLUTIONS AND CELL-DENSITY, Cryobiology, 33(5), 1996, pp. 552-566
Citations number
51
Categorie Soggetti
Biology Miscellaneous",Physiology
Journal title
ISSN journal
00112240
Volume
33
Issue
5
Year of publication
1996
Pages
552 - 566
Database
ISI
SICI code
0011-2240(1996)33:5<552:HSOPH->2.0.ZU;2-T
Abstract
For clinical use of bioartificial liver devices a constant supply of p rimary liver cells has to be provided. Hypothermic storage of isolated pig hepatocytes could support large-scale stocking of cells. Freshly isolated pig hepatocytes from slaughterhouse livers were stored at 4 d egrees C for 24, 48, and 72 h in three different solutions: Leibovitz L-15 + 5% polyethylene glycol (PEG), University of Wisconsin (UW) solu tion, and a simplified UW solution. After storage, cells were cultured for 2 weeks in the collagen sandwich configuration. Viability of hepa tocytes was 65, 85, and 83% after 24 h storage, 21, 74, and 70% after 48 h, and 5, 65, and 59% after 72 h in Leibovitz L-15 medium, UW, and the simplified UW, respectively. After storage in L-15 medium, cells a ttached poorly to collagen matrices and exhibited ultrastructural lesi ons, Functional performance in this group, as judged by albumin secret ion and cytochrome P450-dependent activity in subsequent culture, decr eased rapidly as a function of storage time, with zero values after 48 h storage. In contrast, hypothermia of hepatocytes in both UW solutio ns resulted in well-preserved cells with respect to ultrastructural ap pearance, attachment rates, and functional performance during culture. No significant differences were observed between the original and the simplified UW solution. Higher cell concentrations up to 5 x 10(7) ce lls/ml improved viability of hepatocytes on warmup. in terms of cell s upply for hybrid artificial liver support, hypothermic storage of hepa tocytes at 4 degrees C could mean an alternative to the cryopreservati on of cells, which usually results in a substantial loss of cells and vital function of cells. Thus, pig hepatocytes could be stored at 4 de grees C for several days and meet the logistical need of bioartificial liver devices while avoiding the hazards of cell freezing. (C) 1996 A cademic Press, Inc.