Effects of hypothermia on the function, membrane integrity, and cytoskeletal structure of hepatocytes

Cryobiology. 1995 Aug;32(4):389-403. doi: 10.1006/cryo.1995.1039.

Abstract

To increase the storage time of livers for transplantation, a better understanding of hypothermia-induced hepatocyte damage is necessary. To this end, we have characterized the effects of hypothermia on long-term function and cytoskeletal organization of hepatocytes cultured in the collagen sandwich configuration, which maintains the expression of liver-specific functions for several weeks. In these studies, cultured hepatocytes (maintained at 37 degrees C for 7 days) were exposed to 4 degrees C in Leibovitz-15 (L15), University of Wisconsin (UW) solution, or L15 supplemented with 2.5 g% polyethylene glycol (PEG) for various time periods followed by a return to normothermia. When L15 medium was used, the long-term albumin secretion rate of cultured hepatocytes was decreased by 50% after 4 h, and by 95% after 24 h of exposure to 4 degrees C. Amorphous precipitates of F-actin and fragmented short microtubules were also observed after 4 and 12 h of hypothermia, respectively. Similar results were obtained when hepatocytes were stored in UW solution. However, in L15 supplemented with PEG, no significant reduction in long-term albumin secretion rates and intact actin and microtubule morphology was observed even after 24 h of exposure to 4 degrees C. The membrane integrity and long-term albumin secretion of hepatocytes stored in the presence of PEG were decreased to approximately 50% only after 48 h of exposure to 4 degrees C. Thus, PEG may be a useful additive in preservation solutions for hepatocytes in hepatocyte-based liver support systems and for intact tissue as well.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Actins / metabolism
  • Albumins / metabolism
  • Animals
  • Cell Membrane / physiology
  • Cell Membrane / ultrastructure
  • Cell Survival
  • Cells, Cultured
  • Cold Temperature*
  • Cryopreservation / methods
  • Cytoskeleton / physiology
  • Cytoskeleton / ultrastructure
  • Liver* / cytology
  • Liver* / physiology
  • Microtubules / ultrastructure
  • Rats
  • Time Factors

Substances

  • Actins
  • Albumins