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A freeze-etch study of the effects of extracellular freezing on cellular membranes of wheat

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Abstract

Seedlings of Triticum aestivum L. cv. Lennox were grown in different environments to obtain different hardiness. Pieces of laminae and leaf bases were slowly cooled to sub-zero temperatures and the damage caused was assessed by an ion-leakage method. Comparable pieces of tissue were slowly cooled to temperatures between 2° and-14°C and were then freeze-fixed and freeze-etched. Membranes generally retained their lamellar structures indicated by the abundance of typical membrane fracture faces in all treatments, and some membrane fracture faces had patches which lacked the usual scattering of intramembranous particles (IMP). These IMP-free areas were present in the plasma membrane of tissues given a damaging freezing treatment, but were absent from the plasma membrane of room-temperature controls, of supercooled tissues, and of tissues given a non-damaging freezing treatment. The frequency of IMP-free areas and the proportion of the plasma membrane affected increased with increasing damage. In the most damaged tissue (79% damage; leaf bases exposed to-8°C), 20% of the plasma membrane was IMP-free. The frequencies of IMP at a distance from the IMP-free areas were unaffected by freezing treatments. There was a patchy distribution of IMP in other membranes (nuclear envelope, tonoplast, thylakoids, chloroplast envelope), but only in the nuclear envelope did it appear possible that their occurrence coincided with damage. The IMP-free areas of several membranes were sometimes associated together in stacks. Such membranes lay both to the outside and inside of the plasma membrane, indicating that at least some of the adjacent membrane fragments arose as a result of membrane reorganization induced by the damaging treatment. Occasional views of folded IMP-free plasma membrane tended to confirm this conclusion. The following hypothesis is advanced to explain the damage induced by extracellular freezing. Areas of plasma membrane become free of IMP, probably as a result of the freezing-induced cellular dehydration. The lipids in these IMP-free patches may be in the fluid rather than the gel phase. The formation of these IMP-free patches, especially in the plasma membrane, initiates or involves proliferation and possibly fusion of membranes, and during or following this process, the cells become leaky.

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Abbreviations

EF:

exoplasmatic fracture face

IMP:

intramembranous particles

PF:

protoplasmatic fracture face

References

  • Ahkong, Q.F., Fisher, D., Tampion, W., Lucy, J.A. (1975) Mechanisms of cell fusion. Nature 253, 194–195

    Google Scholar 

  • Branton, D., Bullivant, S., Gilula, N.B., Karnovsky, M.J., Moor, H., Mühlethaler, K., Northcote, D.H., Packer, L., Satir, B., Satir, P., Speth, V., Staehelin, L.A., Steere, R.L., Weinstein, R.S. (1975) Freeze-etching nomenclature. Science 190, 54–56

    Google Scholar 

  • Bullivant, S. (1977) Evaluation of membrane structure, facts and artifacts produced during freeze-fracture. J. Microsc. 111, 101–116

    Google Scholar 

  • Chapman, D. (1975) Phase transitions and fluidity characteristics of lipids and cell membranes. Q. Rev. Biophys. 8, 185–235

    Google Scholar 

  • Cullis, P.R., De Kruijff, B. (1979) Lipid polymorphism and the functional roles of lipids in biological membranes. Biochim. Biophys. Acta 559, 399–420

    Google Scholar 

  • Deamer, D.W., Leonard, R., Tardieu, A., Branton, D. (1970) Lamellar and hexagonal lipid phases visualized by freezeetching. Biochim. Biophys. Acta 219, 47–60

    Google Scholar 

  • Deeley, J.O.T., Coakley, W.T. (1983) Interfacial instability and membrane internalization of human erythrocytes heated in the presence of serum albumin. Biochim. Biophys. Acta 727, 293–302

    Google Scholar 

  • Deuticke, B., Poser, B., Lütkemeier, P., Haest, C.W.M. (1983) Formation of aqueous pores in the human erythrocyte membrane after oxidative cross-linking of spectrin by diamine. Biochim. Biophys. Acta 731, 196–210

    Google Scholar 

  • Dong, H.-z., Sun, L.-h., Jian, L.-c. (1980) Ultrastructural changes in leaf cells of wheat varieties with different cold resistance after freezing-thawing of the plants. Acta Bot. Sinica 22, 341–342

    Google Scholar 

  • Elgsaeter, A., Branton, D. (1974) Intramembrane particle aggregation in erythrocyte ghosts. I. The effects of protein removal. J. Cell Biol. 63, 1018–1030

    Google Scholar 

  • Geiger, B. (1983) Membrane-cytoskeleton interactions. Biochim. Biophys. Acta 737, 305–341

    Google Scholar 

  • Gounaris, K., Sen, A., Brain, A.P.R., Quinn, P.-J., Williams, W.P. (1983) The formation of non-bilayer structures in total polar lipid extracts of chloroplast membranes. Biochim. Biophys. Acta 728, 129–139

    Google Scholar 

  • Gulik-Krzywicki, T., Balerna, M., Vincent, J.P. Lazdunski, M. (1981) Freeze-fracture study of cardiotoxin action on axonal membrane lipid vesicles. Biochim. Biophys. Acta 643, 101–114

    Google Scholar 

  • Gusta, L.V., Burke, M.J., Kapoor, A.C. (1975) Determination of unfrozen water in winter cereals at sub-freezing temperatures. Plant Physiol. 56, 707–709

    Google Scholar 

  • Hay, E.D., Hasty, D.L. (1979) Extension of particle-free membrane blisters during glutaraldehyde fixation. In: Freeze fracture methods, artifacts and interpretations, pp. 59–66, Rash, J.E., Hudson, C.S., eds. Raven Press, New York

    Google Scholar 

  • James, R., Branton, D. (1973) Lipid and temperature dependent structural changes in Acholeplasma laidlawii cell membrane. Biochim. Biophys. Acta 323, 378–390

    Google Scholar 

  • Kleeman, W., Grant, C.W.M., McConnell, H.M. (1974) Lipid phase separations and protein distribution in membranes. J. Supramol. Struct. 2, 609–616

    Google Scholar 

  • Kreissler, M., Lamaire, B., Botharel, P. (1983) Theoretical conformational analysis of phospholipids. I. Role of hydration in the gel to liquid crystal transition of phospholipids. Biochim. Biophys. Acta 735, 23–34

    Google Scholar 

  • Legge, R.L., Thompson, J.E., Baker, J.E., Lieberman, M. (1982) The effects of calcium on the fluidity and phase properties of microsomal membranes isolated from post-climacteric Golden Delicious apples. Plant Cell Physiol. 23, 161–169

    Google Scholar 

  • Lelkes, G., Lelkes, G., Merse, K.A., Hollan, S.R. (1983) Intense reversible aggregation of intramembranous particles in nonhaemolyzed human erythrocytes. A freeze-fracture study. Biochim. Biophys. Acta 732, 48–57

    Google Scholar 

  • Levitt, J. (1980) Responses of plants to environmental stress, 2nd edn. Academic Press, New York London

    Google Scholar 

  • Luzzati, V., Husson, F. (1962) The structure of the liquid-crystalline phases of lipid-water systems. J. Cell Biol. 12, 207–219

    Google Scholar 

  • Mazur, P. (1969) Freezing injury in plants. Annu. Rev. Plant Physiol. 20, 419–448

    Google Scholar 

  • McElhaney, R.N. (1984) The structure and function of the Acholeplasma laidlawii plasma membrane. Biochim. Biophys. Acta 779, 1–42

    Google Scholar 

  • Morris, G.J., Grout, B.W.W. (1984) Letter to the editor: membrane vesiculation — a general cellular response to stress? Cryo-Letters 5, 162–164

    Google Scholar 

  • Nicolson, G.L. (1976) Transmembrane control of the receptors on normal and tumour cells. I. Cytoplasmic influence over cell surface components. Biochim. Biophys. Acta 457, 57–108

    Google Scholar 

  • Palta, J.P., Levitt, J., Stadelmann, E.J. (1977) Freezing tolerance of onion bulb cells and significance of freeze-induced tissue infiltration. Cryobiology 14, 614–619

    Google Scholar 

  • Pearce, R.S. (1980) Relative hardiness to freezing of laminae, roots and tillers of tall fescue. New Phytol. 84, 449–463

    Google Scholar 

  • Pearce, R.S. (1982) Ultrastructure of tall fescue (Festuca arundinacea Schreb. cv. S170) cells fixed while exposed to lethal or non-lethal extracellular freezing. New Phytol. 92, 259–272

    Google Scholar 

  • Pearce, R.S. (1983) A cleaning method ensuring recovery of delicate freeze-fracture replicas of cereal leaf cells. J. Microsc. 129, 229–321

    Google Scholar 

  • Pearce, R.S. (1985) A freeze-fracture study of the cell membranes of wheat adapted to extracellular freezing and to growth at low temperatures. J. Exp. Bot. (in press)

  • Pearce, R.S., McDonald, I. (1977) Ultrastructural damage due to freezing followed by thawing in shoot meristem and leaf mesophyll of cells of tall fescue (Festuca arundinacea Schreb.). Planta 134, 159–168

    Google Scholar 

  • Pearce, R.S., McDonald, I. (1978) The independent assessment of frost hardiness of excised laminae, excised roots and trimmed tillers of tall fescue (Festuca arundinacea). J. Appl. Ecol. 15, 885–895

    Google Scholar 

  • Pearce, R.S., Willison, J.H.M. (1985) Wheat tissues freezeetched during exposure to extracellular freezing: distribution of ice. Planta 163, 295–303

    Google Scholar 

  • Pearce, R.S., Willison, J.H.M. (1984) Tests of a proposed mechanism of feezing damage in wheat seedlings: drought stress induces the same ultrastructural features as extracellular freezing. (Abstr.) Cryobiology (in press)

  • Pearce, R.S., Withers, L.A., Willison, J.H.M. (1974) Bodies of wall-like material (“wall-bodies”) produced intracellularly by cultured protoplasts and plasmolysed cells of higher plants. Protoplasma 82, 223–236

    Google Scholar 

  • Rajashekar, C., Gusta, L.V., Burke, M.J. (1979) Membrane structural transitions: probable relation to frost damage in hardy herbaceous species. In: Low temperature stress in crop plants, the role of the membrane, pp. 255–274, Lvons, J.M., Graham, D., Raison, J.K., eds. Academic Press, New York London

    Google Scholar 

  • Schäfer, G., Rowohl-Quisthoudt, G. (1976) Influence of surface potentials on the mitochondrial H+ pump and on lipid phase transitions. J. Bioenerg. 8, 73–81

    Google Scholar 

  • Seddon, J.M., Kaye, R.D., Marsh, D. (1983) Induction of the lamellar-inverted hexagonal phase transition in cardiolipin by protons and monovalent cations. Biochim. Biophys. Acta 734, 348–352

    Google Scholar 

  • Sen, A., Brain, A.P.R., Quinn, P.J., Williams, W.P. (1982) Formation of inverted lipid micelles in aqueous dispersions of mixed sn-3-galactosyl-diacylglycerols induced by heat and ethylene glycol. Biochim. Biophys. Acta 686, 215–224

    Google Scholar 

  • Simpson, D.J. (1978a) Freeze-fracture studies on barley plastid membranes. I. Wild-type etioplasts. Carlsberg Res. Commun. 43, 145–170

    Google Scholar 

  • Simpson, D.J. (1978b) Freeze-fracture studies on barley plastid membranes. II. Wild-type chloroplasts Carlsberg Res. Commun. 43, 365–389

    Google Scholar 

  • Singh, J. (1979) Ultrastructural alterations in cells of heardened and non-hardened winter rye during hyperosmotic and extracellular freezing stresses. Protoplasma 98, 329–341

    Google Scholar 

  • Speth, V., Wunderlich, F. (1973) Membranes of Tetrahymena. II. Direct visualization of reversible transitions in biomembrane structure induced by temperature. Biochim. Biophys. Acta 291, 621–628

    Google Scholar 

  • Steck, T.L. (1974) The organization of proteins in the human red blood cell membrane. J. Cell Biol. 62, 1–19

    Google Scholar 

  • Steponkus, P.L., Wolfe, J., Dowgert, M.F. (1981) Stresses induced by contraction and expansion during a freeze-thaw cycle: a membrane perspective. In: Effects of low temperature on biological membranes, pp. 307–322, Morris, G.J., Clarke, A., eds. Academic Press, London New York

    Google Scholar 

  • Steponkus, P.L., Dowgert, M.F., Gordon-Kamm, W.J. (1983) Destabilization of the plasma membrane of isolated plant protoplasts during a freeze-thaw cycle: the influence of cold acclimation. Cryobiology 20, 448–465

    Google Scholar 

  • Stout, D.G., Majak, W., Reaney, M. (1980) In vivo detection of membrane injury in freezing temperatures. Plant Physiol. 66, 74–77

    Google Scholar 

  • Thomas, P., Limbrick, A.R., Allan, D. (1983) Limited breakdown of cytoskeletal proteins by an endogenous, protease controls Ca2+-induced membrane fusion events in chicken erythrocytes. Biochim. Biophys. Acta 730, 351–358

    Google Scholar 

  • Van Venetië, R., Verkleij, A.J. (1981) Analysis of the hexagonalII phase and its relations to lipidic particles and the lamellar phase. A freeze-fracture study. Biochim. Biophys. Acta 645, 262–269

    Google Scholar 

  • Verkleij, A.J. (1984) Lipidic intramembranous particles. Biochim. Biophys. Acta 779, 43–63

    Google Scholar 

  • Verkleij, A.J., De Maaga, R., Lennissen-Bijvelt, J., De Kruijff, B. (1982) Divalent cations and chlorpromazine can induce non-bilayer structure in phosphatidic acid-containing model membranes. Biochim. Biophys. Acta 684, 303–327

    Google Scholar 

  • Verkleij, A.J., Ververgaert, P.H.J.T. (1978) Freeze-fracture morphology of biological membranes. Biochim. Biophys. Acta 515, 303–327

    Google Scholar 

  • Wattiaux-De Coninck, S., Dubois, F., Wattiaux, R. (1977) Lateral phase separation and structural integrity of the inner membrane of rat-liver mitochondria, effect of compression, implications in the centrifugation of these organelles. Biochim. Biophys. Acta 471, 421–435

    Google Scholar 

  • Williams, R.J. (1981) Frost dessication: an osmotic model. In: Analysis and improvement of plant cold hardiness, pp. 89–115, Olien, C.R., Smith, M.N., eds. CRC Press, Boca Raton, La.

    Google Scholar 

  • Willison, J.H.M., Rowe, A.J. (1980) Replica shadowing and freeze-etching techniques. North-Holland, Amsterdam

    Google Scholar 

  • Wolfe, J., Steponkus, P.L. (1983a) Mechanical properties of the plasma membrane of isolated plant protoplasts, mechanism of hyperosmotic and extracellular freezing injury. Plant Physiol. 71, 276–285

    Google Scholar 

  • Wolfe, J., Steponkus, P.L. (1983b) Tension in the plasma membrane during osmotic contraction. Cryo-Letters 4, 315–322

    Google Scholar 

  • Yager, P., Chang, E.L. (1983) Destabilization of a lipid nonbilayer phase by high pressure. Biochim. Biophys. Acta 731, 491–494

    Google Scholar 

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Pearce, R.S., Willison, J.H.M. A freeze-etch study of the effects of extracellular freezing on cellular membranes of wheat. Planta 163, 304–316 (1985). https://doi.org/10.1007/BF00395140

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