Skip to main content
Log in

Freeze-induced shrinkage of individual cells and cell-to-cell propagation of intracellular ice in cell chains from salivary glands

  • Research Articles
  • Published:
Experientia Aims and scope Submit manuscript

Abstract

The formation of intracellular ice (IIF), usually a lethal event to be avoided when cryopreserving cells, should, however, be enforced during the cryosurgical destruction of tumour cells. IIF has been investigated so far only in single cells in suspension. Because cells in tissues cannot be successfully cryopreserved, in contrast to single cells in suspension, the mechanism of IIF in tissues may depend on factors that facilitate IIF. We studied IIF in cell strands from salivary glands, which represent a simple form of a tissue. Their cells are connected by channels responsible for intercellular communication. A substantial fraction of cell dehydration during freezing occurs before cells are encapsulated by ice, and the degree of this pre-ice-front shrinkage appears to influence IIF. In strands with coupled cells IIF spread from one cell to adjacent cells in a sequential manner with short delays (200–300 ms), suggesting cell-to-cell propagation via intercellular channels. In strands pretreated with decoupling agents (dinitrophenol, heptanol), sequential IIF was absent. Instead, formation of ice was random, with longer and variable delays between consecutive darkenings indicating IIF. Results suggest that the mechanism of IIF spread, and consequently the degree of cryodamage in tissue, can be influenced by the presence of intercellular channels (gap junctions).

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Literatur

  1. Mazur P. (1963) Kinetics of water loss from cells at subzero temperatures and the likelihood of intracellular freezing. J. Gen. Physiol.47: 347–369.

    PubMed  Google Scholar 

  2. Loewenstein W. R. (1986) Cell-to-cell communication. Permeability, regulation, formation, and functions of the cell-cell membrane channel in cell junctions. In: Physiology of Membrane Disorders, pp. 329–343, Andreoli T. E., Hoffman J. F., Fanestil D. D. and Schultz S. G. (eds), Plenum Publishing Corporation, New York

    Google Scholar 

  3. Politoff A. L., Socolar S. J. and Loewenstein W. R. (1969) Permeability of a cell membrane junciton. Dependence on energy metabolism. J. Gen. Physiol.53: 498–515.

    PubMed  Google Scholar 

  4. Rubinsky B., Arav A. and Devries A. L. (1991) Cryopreservation of oocytes using directional cooling and antifreeze glycoproteins. Cryo-Letters12: 93–106

    Google Scholar 

  5. Loewenstein W. R. and Kanno Y. J. (1964) Studies on an epithelial (gland) cell junction. I. Modifications of surface membrane permeability. J. Cell Biol.22: 565–586

    PubMed  Google Scholar 

  6. Engelmann T. W. (1877) Vergleichende Untersuchungen zur Lehre von der Muskel- und Nervenelektricität. Arch. Ges. Physiol.15: 116–148

    Google Scholar 

  7. Kloetzel J. A. and Laufer H. J. (1969) A fine-structural analysis of larval salivary gland function inChironomus thummi (Diptera). J. Ultrastruct. Res.29: 15–36

    PubMed  Google Scholar 

  8. Körber C., Scheiwe M. W. and Wollhöver K. (1983) Solute polarization during planar freezing of aqueous salt solutions. Int. J. Heat Mass Transfer26: 1241–1253

    Google Scholar 

  9. Leibo S. P., McGrath J. J. and Cravalho E. G. (1978) Microscopic observation of intracellular ice formation in mouse ova as a function of cooling rate. Cryobiology15: 257–271

    PubMed  Google Scholar 

  10. Loewenstein, W. R., Socolar S. J., Higashino S., Kanno Y. and Davidson N. (1965) Intercellular communication: renal, urinary bladder, sensory, and salivary gland cells. Science149: 295–298

    Google Scholar 

  11. Loewenstein W. R., Nakas M. and Socolar S. J. (1967) Junctional membrane uncoupling. Permeability transformations at a cell membrane junction. J. Gen. Physiol.50: 1865–1891

    PubMed  Google Scholar 

  12. Johnston M. F., Simon F. A. and Ramón F. (1980) Interaction of anaesthetics with electrical synapses. Nature286: 498–500

    PubMed  Google Scholar 

  13. Bernardini G., Peracchia C., and Peracchia L. L. (1984) Reversible effects of heptanol on gap junction structure and cell-to-cell electrical coupling. Eur. J. Cell Biol.34: 307–312

    PubMed  Google Scholar 

  14. Toner M., Cravalho E. G. and Karel M. (1990) Thermodynamics and kinetics of intracellular ice formation during freezing of biological cells. J. Appl. Phys.67: 1582–1593

    Google Scholar 

  15. Larese A., Yang H., Petrenko A. and McGann L. E. (1992) Intracellular ice formation is affected by cell-to-cell contact. Cryobiology29: 728, abstract 69

    Google Scholar 

  16. Mazur P. (1965) The role of cell membranes in the freezing of yeast and other single cells. Ann. N. Y. Acad. Sci.125: 658–676

    PubMed  Google Scholar 

  17. Mazur P. (1966) Physical and chemical basis of injury in single-celled microorganisms subjected to freezing and thawing. In: Cryobiology, pp. 213–315, Meryman H. T. (ed.), Academic Press, London

    Google Scholar 

  18. Simpson I., Rose B. and Loewenstein W. R. (1977) Size limits of molecules permeating the junctional membrane channels. Science195: 294–296

    PubMed  Google Scholar 

  19. Flagg-Newton J. L., Simpson I. and Loewenstein W. R. (1979) Permeability of the cell-to-cell membrane channels in mammalian cell junction. Science205: 404–407

    PubMed  Google Scholar 

  20. Schwartzmann G. O. H., Wiegandt H., Rose B., Zimmerman A., Ben-Haim D. and Loewenstein W. R. (1981) The diameter of the cell-to-cell junctional membrane channels, as probed with neutral molecules. Science213: 551–553

    PubMed  Google Scholar 

  21. Meda P. (1994) Molecular biology of gap junction proteins. In: molecular Biology of Diabetes, part 1, pp. 333–356, Draznin B. and LeRoith D. (eds), Humana Press, Totowa, NJ

    Google Scholar 

  22. Meda P., Pepper M. S., Traub O., Willecke K., Gros D., Beyer E., Nicholson B., Paul D. and Orci L. (1993) Differential expression of gap junction connexins in endocrine and exocrine glands. Endocrinology133: 2371–2378

    PubMed  Google Scholar 

  23. Bryant G. (1995) DSC measurement of cell suspensions during successive freezing runs: implications for the mechanisms of intracellular ice formation. Cryobiology32: 114–128

    PubMed  Google Scholar 

  24. Bustamante J. O. and Jachimowicz D. (1988) Cryopreservation of human heart cells. Cryobiology25: 394–408

    PubMed  Google Scholar 

  25. Berger W. K. (1987) Effects of sub-zero temperatures on conduction of action potentials in atrial bundles of the frog heart. Cryo-Letters8: 7–20

    Google Scholar 

  26. Berger W. K. and Tovar O. (1990) On the mechanism of the freeze-induced conduction block of action potentials in rat cardiac muscle. Cryo-Letters11: 35–48

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Berger, W.K., Uhrík, B. Freeze-induced shrinkage of individual cells and cell-to-cell propagation of intracellular ice in cell chains from salivary glands. Experientia 52, 843–850 (1996). https://doi.org/10.1007/BF01938868

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01938868

Key words

Navigation