| Literature DB >> 25936340 |
C F Puts1, T A Berendsen1, B G Bruinsma1, Sinan Ozer1, Martha Luitje1, O Berk Usta1, M L Yarmush2, K Uygun3.
Abstract
Cold storage (at 4°C) offers a compromise between the benefits and disadvantages of cooling. It allows storage of organs or cells for later use that would otherwise quickly succumb to warm ischemia, but comprises cold ischemia that, when not controlled properly, can result in severe damage as well by both similar and unique mechanisms. We hypothesized that polyethylene glycol (PEG) 35 kDa would ameliorate these injury pathways and improve cold primary hepatocyte preservation. We show that reduction of the storage temperature to below zero by means of supercooling, or subzero non-freezing, together with PEG supplementation increases the viable storage time of primary rat hepatocytes in University of Wisconsin (UW) solution from 1 day to 4 days. We find that the addition of 5% PEG 35 kDa to the storage medium prevents cold-induced lipid peroxidation and maintains hepatocyte viability and functionality during storage. These results suggest that PEG supplementation in combination with supercooling may enable a more optimized cell and organ preservation.Entities:
Keywords: Hepatocytes; Lipid peroxidation; Polyethylene glycol; Preservation; Supercooling; University of Wisconsin solution
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Year: 2015 PMID: 25936340 PMCID: PMC4506890 DOI: 10.1016/j.cryobiol.2015.04.010
Source DB: PubMed Journal: Cryobiology ISSN: 0011-2240 Impact factor: 2.487