Oxygen permeability of the lipid bilayer membrane made of calf lens lipids

Biochimica et Biophysica Acta - Biomembranes

Volumn 1768, Issue 10, 2007, Pages 2635-2645

  Widomska, Justyna ^a   Raguz, Marija ^a   Subczynski, Witold K ^a  

^a MEDICAL COLLEGE OF WISCONSIN   (United States)

Author keywords

Cholesterol; EPR; Hydrophobic barrier; Lens lipids; Lipid bilayer; Membrane rigidity; Oxygen permeation

Indexed keywords

2 OLEOYL 1 PALMITOYLPHOSPHATIDYLCHOLINE; CHOLESTEROL; NITROXIDE; OXYGEN; WATER;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CATTLE; CONTROLLED STUDY; CORRELATION COEFFICIENT; GAS PERMEABILITY; LENS; LIPID BILAYER; NONHUMAN; OXYGEN DIFFUSION; OXYGEN TRANSPORT; PRIORITY JOURNAL; SPIN LABELING;

ANIMALS; BIOLOGICAL TRANSPORT; CATTLE; CELL MEMBRANE PERMEABILITY; ELECTRON SPIN RESONANCE SPECTROSCOPY; HYDROPHOBICITY; LENS, CRYSTALLINE; LIPID BILAYERS; OXYGEN;

EID: 34948859469     PISSN: 00052736     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbamem.2007.06.018     Document Type: Article

References (109)

1. Nicholson P., and Roughton F.J.W. A theoretical study of the influence of diffusion and chemical reaction velocity on the rate of exchange of carbon monoxide and oxygen between the red blood corpuscle and surrounding fluid. Proc. R. Soc., B 138 (1951) 241-264
2. 2 and CO with human hemoglobin F in cells and in solution. Respir. Physiol. 3 (1967) 307-317
3. Chan H.-C., Glockner J.F., and Swartz H.M. Oximetry in cells and tissue using a nitroxide-liposome system. Biochim. Biophys. Acta 1014 (1989) 141-144
4. Glockner J.F., Norby S.-W., and Swartz H.M. Simultaneous measurement of intracellular and extracellular oxygen concentration using a nitroxide-liposome system. Magn. Reson. Med. 29 (1993) 12-18
5. Glockner J.F., Swartz H.M., and Pals A. Oxygen gradients in CHO cells: measurement and characterization by electron spin resonance. J. Cell. Physiol. 140 (1989) 505-511
6. Hu H., Sosnovsky G., and Swartz H.M. Simultaneous measurements of the intra- and extra-cellular oxygen concentration in viable cells. Biochim. Biophys. Acta 1112 (1992) 161-166
7. Swartz H.M. Measurements of intracellular concentration of oxygen: experimental results and conceptual implications of an observed gradient between intracellular and extracellular concentrations of oxygen. In: Vaupel P., Zander R., and Burley D.F. (Eds). Oxygen Transport to Tissue XV, Advances in Experimental Medicine and Biology vol. 345 (1994), Plenum, New York 799-806
8. Subczynski W.K., and Swartz H.M. EPR oximetry in biological and model samples. In: Eaton S.S., Eaton G.R., and Berliner L.J. (Eds). Biological Magnetic Resonance. Biomedical EPR-Part A: Free Radicals, Metals, Medicine, and Physiology vol. 23 (2005), Kluwer/Plenum, New York 229-282
9. Subczynski W.K., Hyde J.S., and Kusumi A. Oxygen permeability of phosphatidylcholine-cholesterol membranes. Proc. Natl. Acad. Sci. U. S. A. 86 (1989) 4474-4478
10. Subczynski W.K., Hyde J.S., and Kusumi A. Effect of alkyl chain unsaturation and cholesterol intercalation on oxygen transport in membranes: a pulse ESR spin labeling study. Biochemistry 30 (1991) 8578-8590
11. Ashikawa I., Yin J.-J., Subczynski W.K., Kouyama T., Hyde J.S., and Kusumi A. Molecular organization and dynamics in bacteriorhodopsin-rich reconstituted membranes: discrimination of lipid environments by the oxygen transport parameter using a pulse ESR spin-labeling technique. Biochemistry 33 (1994) 4947-4952
12. Kawasaki K., Yin J.-J., Subczynski W.K., Hyde J.S., and Kusumi A. Pulse EPR detection of lipid exchange between protein-rich raft and bulk domains in the membrane: methodology development and its application to studies of influenza viral membrane. Biophys. J. 80 (2001) 738-748
13. Li L.K., So L., and Spector A. Membrane cholesterol and phospholipids in consecutive concentric sections of human lenses. J. Lipid Res. 26 (1985) 600-609
14. Li L.K., So L., and Spector A. Age-dependent changes in the distribution and concentration of human lens cholesterol and phospholipids. Biochim. Biophys. Acta 917 (1987) 112-120
15. Byrdwell W.C., Borchman D., Porter R.A., Taylor K.G., and Yappert M.C. Separation and characterization of the unknown phospholipids in human lens membranes. Investig. Ophthalmol. Vis. Sci. 35 (1994) 4333-4343
16. Byrdwell W.C., and Borchman D. Lipid chromatography/mass-spectrometric of sphingomyelin and dihydrosphingomyelin of human lens membranes. Ophthalmic Res. 29 (1997) 191-206
17. Varadaraj K., Kushmerick C., Baldo G.J., Bassnett S., Shiels A., and Mathias R.T. The role of MIP in lens fiber cell membrane transport. J. Membr. Biol. 170 (1999) 191-203
18. Truscott R. Age-related nuclear cataract: a lens transport problem. Ophthalmic Res. 32 (2000) 185-194
19. Huang L., Grami V., Marrero Y., Tang D., Yappert M.C., Rasi V., and Borchman D. Human lens phospholipid change with age and cataract. Investig. Ophthalmol. Vis. Sci. 46 (2005) 1682-1689
20. Broekhuyse R.M., and Kuhlmann E.D. Lens membrane I. Composition of urea-treated plasma membranes of calf lens. Exp. Eye Res. 19 (1974) 297-302
21. Broekhuyse R.M., and Kuhlmann E.D. Lens membrane IV. Preparative isolation and characterization of membranes and various membrane proteins from calf lens. Exp. Eye Res. 26 (1978) 305-320
22. Gooden M.M., Takemoto L.J., and Rintoul D.A. Evidence for reduced lipid order in plasma membranes from cataractous human lenses. Curr. Eye Res. 2 (1983) 367-375
23. Rafferty N.S. Lens morphology. In: Maisel H. (Ed). The Ocular Lens: Structure, Function and Pathology (1985), Marcel Dekker, New York 1-60
24. Broekhuyse R.M., and Soeting W.J. Lipids in tissue of the eye: XV. Essential fatty acids in lens lipids. Exp. Eye Res. 22 (1976) 653-657
25. Zelenka P.S. Phospholipid composition and metabolism in the embryonic chicken lens. Exp. Eye Res. 26 (1978) 267-274
26. Borchman D., Yappert M.C., and Afzal M. Lens lipids and maximum lifespan. Exp. Eye Res. 79 (2004) 761-768
27. Widomska J., Raguz M., Dillon J., Gaillard E.R., and Subczynski W.K. Physical properties of the lipid bilayer membrane made of calf lens lipids: EPR spin labeling studies. Biochim. Biophys. Acta 1768 (2007) 1454-1465
28. Huang L., Estrada R., Yappert M.C., and Borchman D. Oxidation-induced changes in human lens epithelial cells 1. Phospholipids. Free Radic. Biol. Med. 41 (2006) 1425-1432
29. McNulty R., Wang H., Mathias R.T., Ortwerth B.J., Truscott R.J.W., and Bassnett S. Regulation of tissue oxygen levels in the mammalian lens. J. Physiol. 559 (2004) 883-898
30. Eaton J.W. Is the lens canned?. Free Radic. Biol. Med. 11 (1991) 207-213
31. Harding J.J. Cataract. Biochemistry, Epidemiology and Pharmacology (1991), Chapman and Hall, London
32. Jacobi K.W., and Driest J. Oxygen determinations in the vitreous body of the living eye, Ber Zusammenkunft Dtsch. Ophthalmol. Ges. 67 (1966) 193-198
33. Briggs D., and Rodenhauser J.H. Distribution and consumption of oxygen in the vitreous body of cats. In: Kessler M. (Ed). Oxygen Supply: Theoretical and Practical Aspects of Oxygen Supply and Microcirculation of Tissue (1973), University Park Press, Baltimore 265-269
34. Ormerod L.D., Edelstein M.A., Schmidt G.J., Juarez R.S., Finegold S.M., and Smith R.E. The intraocular environment and experimental anaerobic bacterial endophthalmitis. Arch. Ophthalmol. 105 (1987) 1571-1575
35. Fitch C.L., Swedberg S.H., and Livesey J.C. Measurement and manipulation of the partial pressure of oxygen in the rat anterior chamber. Curr. Eye Res. 20 (2000) 121-126
36. Bassnett S., and McNulty R. The effect of elevated intraocular oxygen on organelle degradation in the embryonic chicken lens. J. Exp. Biol. 206 (2003) 4353-4361
37. Barbazetto I.A., Liang J., Chang S., Zheng L., Spector A., and Dillon J.P. Oxygen tension in the rabbit lens and vitreous before and after vitrectomy. Exp. Eye Res. 78 (2004) 917-924
38. Shui Y.-B., Garcia C., Dattilo L.K., Rajagopal R., McMillan S., Mak G., Holekamp N.M., Lewis A., and Beebe D.C. Oxygen distribution in the rabbit eye and oxygen consumption by the lens. Investig. Ophthalmol. Vis. Sci. 47 (2006) 1571-1580
39. Palmquist B.M., Philipson B., and Barr P.O. Nuclear cataract and myopia during hyperbaric oxygen therapy. Br. J. Ophthalmol. 68 (1984) 113-117
40. Chung C.P., Hsu S.Y., and Wu W.C. Cataract formation after pars plana vitrectomy, Kaohsiung. J. Med. Sci. 17 (2001) 84-89
41. Hsuan J.D., Brown N.A., Bron A.J., Petel C.K., and Rosen P.H. Posterior subcapsular and nuclear cataract after vitrectomy. J. Cataract Refract. Surg. 27 (2001) 437-444
42. Holekamp N.M., Shui Y.-B., and Beebe D.C. Vitrectomy surgery increases oxygen exposure to the lens: a possible mechanism for nuclear cataract formation. Am. J. Ophthalmol. 139 (2005) 302-310
43. Uyama C. Diffusion model of a cat eye. In: Kessler M. (Ed). Oxygen Supply: Theoretical and Practical Aspects of Oxygen Supply and Microcirculation of Tissue (1973), University Park Press, Baltimore 64-66
44. Helbig H., Hinz J.P., Kellner U., and Foerster M.H. Oxygen in the anterior chamber of the human eye. Ger. J. Ophthalmol. 2 (1993) 161-164
45. Fischkoff S., and Vanderkooi J.M. Oxygen diffusion in biological and artificial membranes determined by the fluorochrome pyrene. J. Gen. Physiol. 65 (1975) 663-676
46. Coin D.T., and Olson J.S. The rate of oxygen uptake by human red blood cells. J. Biol. Chem. 254 (1979) 1178-1190
47. Huxley V.H., and Kutchai M.J. The effect of the red cell membrane and a diffusion boundary layer on the rate of oxygen uptake by human erythrocytes. J. Physiol. 316 (1981) 75-83
48. Huxley V.H., and Kutchai M.J. Effects of diffusion boundary layers on the initial uptake of oxygen by red blood cells: theory vs. experiments. Microvasc. Res. 26 (1983) 89-107
49. Kimich R., and Peters A. Solvation of oxygen in lecithin bilayers. Chem. Phys. Lipids 14 (1975) 350-362
50. Peters A., and Kimich R. The heterogenious solubility of oxygen in aqueous lecithin dispersion and its relation to chain mobility. NMR relaxation and wide-line study. Biophys. Struct. Mech. 4 (1978) 67-85
51. Battino R., Evans F.D., and Danforth W.F. Solubility of seven gases in olive oil with reference to theories of transport through the cell membrane. J. Am. Oil Chem. Soc. 45 (1968) 830-833
52. Windrem D.A., and Plachy W.Z. The diffusion-solubility of oxygen in lipid bilayers. Biochim. Biophys. Acta 600 (1980) 655-665
53. Kusumi A., Subczynski W.K., and Hyde J.S. Oxygen transport parameter in membranes as deduced by saturation recovery measurements of spin-lattice relaxation times of spin labels. Proc. Natl. Acad. Sci. U. S. A. 79 (1982) 1854-1858
54. 2) method to measure oxygen permeability of phospholipids bilayer and its use to study the effect of low ethanol concentration. J. Magn. Reson., Ser. B 111 (1996) 149-157
55. Subczynski W.K., Lewis R.N.A.H., McElhaney R.N., Hodges R.S., Hyde J.S., and Kusumi A. Molecular organization and dynamics of 1-palmitoyl-2-oleoylphosphatidylcholine bilayers containing a transmembrane α-helical peptide. Biochemistry 37 (1998) 3156-3164
56. Marsh D. Polarity and penetration profiles in lipid membranes. Proc. Natl. Acad. Sci. U.S.A. 98 (2001) 7777-7782
57. Subczynski W.K., Pasenkiewicz-Gierula M., McElhaney R.N., Hyde J.S., and Kusumi A. Molecular dynamics of 1-palmitoyl-2-oleoylphosphatidylcholine membranes containing transmembrane α-helical peptides with alternating leucine and alanine residues. Biochemistry 42 (2003) 3939-3948
58. Subczynski W.K., Hopwood L.E., and Hyde J.S. Is the mammalian cell plasma membrane a barrier to oxygen transport?. J. Gen. Physiol. 100 (1992) 69-87
59. Hyde J.S., and Subczynski W.K. Simulation of ESR spectra of the oxygen-sensitive spin-label probe CTPO. J. Magn. Reson. 56 (1984) 125-130
60. Subczynski W.K., and Hyde J.S. Diffusion of oxygen in water and hydrocarbons using an electron spin resonance spin-label technique. Biophys. J. 45 (1984) 743-748
61. Hyde J.S., and Subczynski W.K. Spin-label oximetry. In: Berliner L.J., and Reuben J. (Eds). Biological Magnetic Resonance. Spin Labeling: Theory and Applications vol. 8 (1989), Plenum, New York 399-425
62. Zaccai G., Büldt G., Seelig A., and Seelig J. Neutron diffraction studies on phosphatidylcholine model membranes II. Chain conformation and segmental disorder. J. Mol. Biol. 134 (1979) 693-706
63. Janiak M.J., Small D.M., and Shipley G.G. Nature of the thermal pretransition of synthetic phospholipids: dimyristoyl- and dipalmitoyllecithin. Biochemistry 15 (1976) 4575-4580
64. Cornell B.A., and Separovic F. Membrane thickness and acyl chain length. Biochim. Biophys. Acta 733 (1983) 189-193
65. Lis L.J., MacAlister M., Fuller N., and Rand R.P. Interactions between neutral phospholipids bilayer membranes. Biophys. J. 37 (1982) 657-665
66. Kucerka N., Tristram-Nagle S., and Nagle J.F. Structure of fully hydrated fluid phase lipid bilayers with monounsaturated chains. J. Membr. Biol. 208 (2005) 193-202
67. Pandit S.A., Chiu S.-W., Jakobsson E., Grama A., and Scott H.L. Cholesterol surrogates: a comparison of cholesterol and 16:0 ceramide in POPC bilayers. Biophys. J. 92 (2007) 920-927
68. McIntosh T.J. The effect of cholesterol on the structure of phosphatidylcholine bilayers. Biochim. Biophys. Acta 513 (1978) 43-58
69. Franks N.P., and Lieb W.R. The structure of lipid bilayers and the effects of general anaesthetics. An X-ray and neutron diffraction study. J. Mol. Biol. 133 (1979) 469-500
70. Nagle J.F., and Wilkinson D.A. Lecithin bilayers. Density measurement and molecular interactions. Biophys. J. 23 (1978) 159-175
71. Janiak M.J., Small D.M., and Shipley G.G. Temperature and compositional dependence of the structure of hydrated dimyristoyl lecithin. J. Biol. Chem. 254 (1979) 6068-6078
72. Levine Y.K., and Wilkins M.H.F. Structure of Oriented Lipid Bilayers. Nat. New Biol. 230 (1971) 69-72
73. Groebe K., and Vaupel P. Evaluation of oxygen diffusion distance in human cancer xenografts using tumor-specific in vivo data: role of various mechanisms in the development of tumor hypoxia. Int. J. Radiot. Oncol. Biol. Phys. 15 (1988) 691-697
74. Hitchman M. Measurements of Dissolved Oxygen (1964), John Wiley and Sons, New York
75. Grote J., Susskind R., and Vaupel P. Oxygen diffusivity in tumour tissue (DS-carcinosarcoma) under temperature conditions within the rang of 20-40 degrees C. Pflugers Arch. 372 (1977) 37-42
76. Merkle H., Subczynski W.K., and Kusumi A. Dynamic fluorescence quenching studies on lipid mobilities in phosphatidylcholine-cholesterol membranes. Biochim. Biophys. Acta 897 (1987) 238-248
77. Yin J.-J., Feix J.B., and Hyde J.S. Mapping of collision frequencies for stearic acid spin labels by saturation-recovery electron paramagnetic resonance. Biophys. J. 58 (1990) 713-720
78. Yin J.-J., and Subczynski W.K. Effect of lutein and cholesterol on alkyl chain bending in lipid bilayers: a pulse electron paramagnetic resonance spin labeling study. Biophys. J. 71 (1996) 832-839
79. St. Denis C.E., and Fell C.J. Diffusivity of oxygen in water. Can. J. Chem. Eng. 49 (1971) 885
80. Lieb W.R., and Stein W.D. Simple diffusion across the membrane bilayer. In: Stein D. (Ed). Transport and Diffusion across Cell Membranes (1986), Academic Press, Orlando 69-112
81. Power G.G., and Stegall H. Solubility of gases in human red blood cell ghosts. J. Appl. Physiol. 29 (1970) 145-149
82. Katz Y., and Diamond J.M. Thermodynamic constants for nonelectrolyte partition between dimyristoyl lecithin and water. J. Membr. Biol. 17 (1974) 101-120
83. Dix J.A., Kivelson D., and Diamond J.M. Molecular motion of small nonelectrolyte molecules in lecithine bilayer. J. Membr. Biol. 40 (1978) 315-342
84. Subczynski W.K., and Hyde J.S. Concentration of oxygen in lipid bilayer using a spin-label method. Biophys. J. 41 (1983) 283-286
85. Smotkin E.S., Moy F.T., and Plachy W.Z. Dioxygen solubility in aqueous phosphatidylcholine dispersion. Biochim. Biophys. Acta 1061 (1991) 33-38
86. Subczynski W.K., Wisniewska A., Yin J.-J., Hyde J.S., and Kusumi A. Hydrophobic barrier of lipid bilayer membranes formed by reduction of water penetration by alkyl chain unsaturation and cholesterol. Biochemistry 33 (1994) 7670-7681
87. E. Overton, Ueber die allgemeinen osmotischen Eigenschaften der Zelle, ihre vermutlichen Ursachen und ihre Bedoutung für die Physiologie (Translated by R. B. Park, On the general osmotic properties of the cell, their probable origin, and their significance for physiology in: D. Branton, R. B. Park (Eds.), Papers on Biological membrane Structure, Little, Brown and Co., Boston, 1968), Vierteljahrsschr Naturforsch. Ges., Zürich 44 (1899) 88-135.
88. Diamond J.M., and Katz Y. Interpretation of nonelectrolyte partition coefficients between dimyristoyl lecithin and water. J. Membr. Biol. 17 (1974) 121-154
89. Walter A., and Gutknecht J. Permeability of small nonelectrolytes through lipid bilayer membranes. J. Membr. Biol. 90 (1986) 207-217
90. Leahy D.E., and Wait A.R. Solute transport resistance at water-oil interface. J. Pharm. Sci. 75 (1986) 1157-1161
91. Subczynski W.K., and Hyde J.S. Membranes: barriers or pathways for oxygen transport. In: Hudetz A.G. (Ed). Oxygen Transport to Tissue XX, Advances in Experimental Medicine and Biology vol. 345 (1998), Plenum, New York 799-806
92. Subczynski W.K., Wisniewska A., Hyde J.S., and Kusumi A. Three-dimensional dynamic structure of the liquid-ordered domain in lipid membranes as examined by pulse-EPR oxygen probing. Biophys. J. 92 (2007) 1573-1584
93. Griffith O.H., Dehlinger P.J., and Van S.P. Shape of the hydrophobic barrier of phospholipids bilayers (Evidence for water penetration into biological membranes). J. Membr. Biol. 15 (1974) 159-192
94. Skulachev V.P. Power transmission along biological membranes. J. Membr. Biol. 114 (1990) 97-112
95. Broekhuyse R.M. Membrane lipids and proteins in ageing lens and cataract. Ciba Found. Symp. 19 (1973) 135-149
96. Roy D., Rosenfeld L., and Spector A. Lens plasma membrane: isolation and biochemical characterization. Exp. Eye Res. 35 (1982) 113-129
97. Truscott R.J.W. Age-related nuclear cataract: a lens transport problem. Ophthalmic Res. 32 (2000) 185-194
98. Bach D., and Wachtel E. Phospholipid/cholesterol model membranes: formation of cholesterol crystallites. Biochim. Biophys. Acta 1610 (2003) 187-197
99. Borchman D., Cenedella R.J., and Lamba O.P. Role of cholesterol in the structural order of lens membrane lipids. Exp. Eye Res. 62 (1996) 191-197
100. Jacob R.F., Cenedella R.J., and Mason R.P. Direct evidence for immiscible cholesterol domains in human ocular lens fiber cell plasma membranes. J. Biol. Chem. 274 (1999) 31613-31618
101. Jacob R.F., Cenedella R.J., and Mason R.P. Evidences for distinct cholesterol domains in fiber cell membranes from cataractous human lenses. J. Biol. Chem. 276 (2001) 13573-13578
102. Mason R.P., Tulenko T.N., and Jacob R.F. Direct evidence for cholesterol crystalline domains in biological membranes: role in human pathobiology. Biochim. Biophys. Acta 1610 (2003) 198-207
103. Munro S. Lipid rafts: elusive or illusive. Cell 115 (2003) 377-388
104. Yappert M.C., and Borchman D. Sphingolipids in human lens membranes: an update on their composition and possible biological implication. Chem. Phys. Lipids 129 (2004) 1-20
105. Borchman D., and Tang D. Binding capacity of α-crystallin to bovine lens lipids. Exp. Eye Res. 63 (1996) 407.α-410.α
106. Tang D., Borchman D., and Yappert M.C. Alpha-crystallin/lens lipid interactions using resonance energy transfer. Ophthalmic Res. 31 (1999) 452-462
107. Grami V., Marrero Y., Huang L., Tang D., Yappert M.C., and Borchman D. α-Crystallin binding in vitro to lipids from clear human lenses. Exp. Eye Res. 81 (2005) 138-146
108. Altenbach C., Greenhalgh D.A., Khorana H.G., and Hubbell W.L. A collision gradient method to determine the immersion depth of nitroxides in lipid bilayers: application to spin-labeled mutants of bacteriorhodopsin. Proc. Natl. Acad. Sci. U. S. A. 91 (1994) 1667-1671
109. Subczynski W.K., Renk G.E., Crouch R.K., Hyde J.S., and Kusumi A. Oxygen diffusion-concentration product in rhodopsin as observed by a pulse ESR spin labeling method. Biophys. J. 63 (1992) 573-577