ANTIFREEZE GLYCOPROTEINS PROMOTE INTRACELLULAR FREEZING OF RAT CARDIOMYOCYTES AT HIGH SUBZERO TEMPERATURES

Citation
Ja. Mugnano et al., ANTIFREEZE GLYCOPROTEINS PROMOTE INTRACELLULAR FREEZING OF RAT CARDIOMYOCYTES AT HIGH SUBZERO TEMPERATURES, American journal of physiology. Regulatory, integrative and comparative physiology, 38(2), 1995, pp. 474-479
Citations number
26
Categorie Soggetti
Physiology
ISSN journal
03636119
Volume
38
Issue
2
Year of publication
1995
Pages
474 - 479
Database
ISI
SICI code
0363-6119(1995)38:2<474:AGPIFO>2.0.ZU;2-J
Abstract
Despite recent reports that antifreeze glycoproteins (AFGPs) protect m ammalian cells during low-temperature preservation, T. Wang, Q. Zhu, X . Yang, J. R. Layne, and A. L. DeVries (Cryobiology 31: 185-192, 1994) reported that AFGPs failed to protect rat hearts during freezing. Rat her, the presence of AFGPs exacerbated cardiac damage after freezing. This study examined the effects of freezing (-4 degrees C) in the pres ence of AFGPs at the cellular level with the use of cryomicroscopy. La rge, blunt ice crystals formed in the solutions without AFGPs and excl uded most cardiomyocytes from the plane of ice formation. After thawin g, cells appeared similar in morphology to unfrozen cells. Ice in 0.5 mg/ml AFGP solution was more dendritic and prismatic than ice formed i n the absence of AFGPs. On thawing, many cells exhibited spontaneous c ontraction, resulting in cell death. Spicular ice formed rapidly in th e 10 mg/ml AFGP solution. These needlelike ice crystals appeared to pe netrate the cardiomyocytes, resulting in intracellular freezing follow ed by cell lysis. These AFGP-induced changes in ice crystal structure may account for the injury observed in whole heart and cardiomyocyte e xperiments.