Polyethylene glycol protects primary hepatocytes during supercooling preservation

被引:32
|
作者
Puts, C. F. [1 ,2 ]
Berendsen, T. A. [1 ,2 ]
Bruinsma, B. G. [1 ,2 ]
Ozer, Sinan [1 ,2 ]
Luitje, Martha [1 ,2 ]
Usta, O. Berk [1 ,2 ]
Yarmush, M. L. [1 ,2 ,3 ]
Uygun, K. [1 ,2 ]
机构
[1] Massachusetts Gen Hosp, Dept Surg, Ctr Engn Med, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Cambridge, MA 02138 USA
[3] Rutgers State Univ, Dept Biomed Engn, Piscataway, NJ USA
基金
美国国家卫生研究院;
关键词
Hepatocytes; Preservation; Supercooling; University of Wisconsin solution; Lipid peroxidation; Polyethylene glycol; COLLAGEN SANDWICH; COLD; TRANSPLANTATION; PEROXIDATION; MEMBRANES; SURVIVAL; BEHAVIOR; RAT;
D O I
10.1016/j.cryobiol.2015.04.010
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cold storage (at 4 degrees 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. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:125 / 129
页数:5
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