Cell contact with solid surfaces

  • David Gingell
Part of the Springer Series in Biophysics book series (BIOPHYSICS, volume 5)

Abstract

It is my intention to outline the main biophysical studies on cell-to-substratum contact which have been done in this laboratory during the past few years. A brief explanation of the way in which the topics to be discussed are connected may be helpful. In the dark ages, when it was suspected that cell adhesion could be understood solely as a long-range balance of intermolecular attractive and repulsive forces, without direct molecular contact, I joined Dr.V.A.Parsegian to learn how to calculate the size of these forces (Parsegian & Gingell, 1973) and went on to devise several ways of measuring them for cell contacts. Since the idea of a long-range force balance implies a gap between the cell membrane and the substratum, it was natural to try to visualize it optically and measure it if possible. This led to an interest in interferometry which eventually culminated in a quantitative theory of interference reflection microscopy, IRM, (Gingell & Todd, 1979; Gingell et al., 1982). Cell-to-substratum water gaps were indeed detected in certain situations for aldehyde-fixed red blood cells (Gingell & Todd, 1980) and for free living amoebae (Gingell & Vince, 1982b). The theory helped us to understand why IRM images could sometimes be very hard to interpret, and our attention turned to total internal reflection fluorescence as an alternative and superior method of visualizing and measuring cell-to substratum contacts. The success of this technique has exceeded our most optimistic predictions.

Keywords

Hydration Hydrocarbon Interferon Polystyrene Choline 

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References

  1. Andrade, J.D. (1985) Surface and interfacial aspects of biomedical polymers, vol.1 Surface chemistry and physics. Editor, J.D. Andrade. Plenum Press, New York and London.Google Scholar
  2. Avnur, Z. fit Geiger, B. (1981) The removal of extracellular fibronectin from areas of cell-substrate contact. Cell 25: 121–132PubMedCrossRefGoogle Scholar
  3. Axelrod, D. (1981) Cell substrate contacts illuminated by total internal reflection fluorescence. J.Cell Biol., 89: 141–145PubMedCrossRefGoogle Scholar
  4. Bailey, J. & Gingell, D. (1988) Contacts of chick fibroblasts on glass: results and limitations of quantitative interferometry. J.Cell Sci., 90: 215–224PubMedGoogle Scholar
  5. Boresnstein, N. & Brash, J.L. (1986) Red blood cells deposit membrane components on contacting surfaces. J.Biomed. Mater. Res., 20: 723–730CrossRefGoogle Scholar
  6. Brash, J.L. (1983) Hydrophobic polymer surfaces and their interaction with blood. Ann. N.Y. Acad. Sci., 283: 356–371CrossRefGoogle Scholar
  7. Chasis, J.A., Reid, M.E., Jensen, R.H. & Mohandas, N. (1988) Signal transduction by glycophorin A: role of extracellular and cytoplasmic domains in a modulatable process. J.Cell Biol., 107: 1351–1357PubMedCrossRefGoogle Scholar
  8. Chipowsky, S., Lee, Y.C. fit Roseman, S. (1973) Adhesion of cultured fibroblasts to insoluble analoques of cell-surface carbohydrates. Proc. Natl. Acad. Sci. USA 70: 2309–2312PubMedCrossRefGoogle Scholar
  9. Curtis, A.S.G. (1962) Cell contact and adhesion. Biol.Rev., 37: 82–129PubMedCrossRefGoogle Scholar
  10. Curtis, A.S.G., Forrester, J.V., McInnes, C. fit Lawrie, F. (1983) Adhesion of cells to polystyrene surfaces. J.Cell Biol., 97: 1500–1506PubMedCrossRefGoogle Scholar
  11. Durrani, A.A., Hayward, J.A. fit Chapman, D. (1986) Biomembranes as models for polymer surfaces. 11. The synthesis of reactive species for covalent coupling of phosphorylcholine to polymer surfaces. Biomaterials, 7: 121–125PubMedCrossRefGoogle Scholar
  12. Feltkamp, C.A., Spiele, H. fit Roos, E. (1987) Interaction of plasma membrane-associated filaments and H2 histocompatibility antigens before and after induced patching and capping. J.Cell Sci., 88: 313–325PubMedGoogle Scholar
  13. Francis, G.W., Fisher, L.R., Gamble, R.A. & Gingell, D. (1987) Direct measurement of cell detachment force on single cells using a new electromechanical method. J.Cell Sci., 87: 519–523PubMedGoogle Scholar
  14. Gingel1, D. (1981) The interpretation of interference reflection images of spread cells: significant contributions from thin peripheral cytoplasm. J.Cell Sci., 49: 237–247PubMedGoogle Scholar
  15. Gingell, D. fit Fornes, J.A. (1976) Interaction of red blood cells with a polarized electrode: evidence of long-range intermolecular forces. Biophys.J., 16: 1131–1135PubMedCrossRefGoogle Scholar
  16. Gingell, D., Heavens, O.S. & Mellor, J.S. (1987) General electromagnetic theory of total internal reflection fluorescence: the quantitative basis for mapping cell-substratum topography. J.Cell Sci., 87: 677–693PubMedGoogle Scholar
  17. Gingell, D. fit Todd, I. (1979) Interference reflection microscopy. A quantitative theory for image interpretation and its application to cell-substratum separation measurement. Biophys.J., 26: 507–526PubMedCrossRefGoogle Scholar
  18. Gingell, D. & Todd, I. (1980) Red blood adhesion. 11. Interferometric examination of the interaction with hydrocarbon and glass. J.Cell Sci., 41: 135–149PubMedGoogle Scholar
  19. Gingell, D., Todd, I. & Bailey, J. (1985) Topography of cell-glass apposition revealed by total internal reflection fluorescence of volume markers. J.Cell Biol., 100: 1334–1338PubMedCrossRefGoogle Scholar
  20. Gingell, D., Todd, I. & Heaven, O.S. (1982) Quantitative interference microscopy: effect of microscope aperture. Optica Acta, 29: 901–908CrossRefGoogle Scholar
  21. Gingell, D., Todd, I. & Parsegian, V.A. (1977) Long-range attaction between red cells and a hydrocarbon surface. Nature, 268: 767–769PubMedCrossRefGoogle Scholar
  22. Gingell, D. & Vince, S. (1982a) Substratum wettability and charge influence the spreading of Dictyostelium amoebae and the formation of ultrathin cytoplasmic lamellae. J.Cell Sci., 54: 255–285Google Scholar
  23. Gingell, D. & Vince, S. (1982b) Cell-glass separation depends on salt concentration and valency: measurements on Dictyostelium amoebae by finite aperture interferometry. J.Cell Sci., 54: 299–310Google Scholar
  24. Grinnell, F. (1986) Focal adhesion sites and the removal of substratum-bound fibronectin. J.Cell Biol., 103: 2697–2706PubMedCrossRefGoogle Scholar
  25. Hafeman, D.D., von Tscharner, V. & McConnell, H.M. (1981) Specific antibody-dependent interaction between macrophages and lipid haptens in polar lipid monolayers. Proc. Natl. Acad. Sci. U.S.A., 78: 4552–4556PubMedCrossRefGoogle Scholar
  26. Izzard, C.S. & Lochner, L.R. (1976) Cell-to-substrate contacts in living fibroblasts: an interference reflexion study with an evaluation of the technique. J.Cell Sci., 21: 129–159PubMedGoogle Scholar
  27. Kane, P.M., Holowka, D. & Baird, B. (1988) Cross-linking of IgE-receptor complexes by rigid bivalent antigens >200A in length triggers cellular degranulation. J.Cell Biol. 107: 969–980PubMedCrossRefGoogle Scholar
  28. Klein, J. & Luckham, P. (1982) Forces between two adsorbed polyethylene oxide layers immersed in a good aqueous solvent. Nature, 300: 429–431CrossRefGoogle Scholar
  29. Le Neveu, D.M., Rand, R.P., Parsegian, V.A. & Gingell, D. (1977) Measurement and modification of forces between lecithin bilayers. Biophys.J., 18: 209–230CrossRefGoogle Scholar
  30. Luckham, P.F. & Klein, J.K. (1985) Forces between mica surfaces bearing adsorbed polyelectrolytes. J.Chem. Soc. Faraday Trans. 1. 80:865–878Google Scholar
  31. Margolis, L.B., Dyatlovitskaya, E.V. & Bergelson, L.D. (1978) Cell-lipid interactions. Cell attachment to lipid substrates. Expl. Cell Res., 111: 454–457CrossRefGoogle Scholar
  32. McConnell, H.M., Watts, T.H., Weis, R.M. & Brian, A.A. (1986) Supported planar membranes in studies of cell-cell recognition in the immune system. Biochim. Biophys. Acta, 864: 95–106PubMedGoogle Scholar
  33. Mellor, J.S., Gingell, D. & Heavens, O.S. (1988) Measurement of the thickness of deposited magnesium fluoride films by evanescent wave fluorescence: a critical test of the general TIRAF theory. J.Modern Optics, 35: 623–628CrossRefGoogle Scholar
  34. Metzger, H. (1983) The receptor on mast cells and related cells with high affinity for IgE. Contemp. Top. Mol. Immunol., 9: 115–145PubMedGoogle Scholar
  35. Mori, Y., Nagaska, S., Takiuchi, H., Kikuchi, T., Noguchi, N., Tanzawa, H. & Noishiki, Y. (1982) A new antithrombogenic material with long polyethyleneoxide chains. Trans. Am. Soc. Artif. Int. Organs, 28: 459–462Google Scholar
  36. Neyfakh, A.A., Tint, I.S., Svitkina, A.D., Bershadsky, A.D. & Gelfand, V.I. (1983) Visualization of cellular focal contacts using a monoclonal antiboby to 80 kD serum protein adsorbed on the substratum. Exp. Cell Res., 149: 387–396PubMedCrossRefGoogle Scholar
  37. Norde, W., MacRitchie, F., Nowicka, G, & Lyklema, J. (1986) Protein adsorption at solid-liquid interfaces: reversibility and conformational aspects. J.Coll. Interface Sci., 112: 447–456CrossRefGoogle Scholar
  38. Owens, N.F., Gingell, D. & Bailey, J. (1988a) Contact-mediated triggering of lamella formation by Dictyostelium amoebae on solid surfaces. J.Cell Sci., 91: 367–377PubMedGoogle Scholar
  39. Owens, N.F., Gingell, D. & Rutter, P.R. (1987) Inhibition of cell adhesion by a synthetic polymer adsorbed to glass shown under defined hydrodynamic stress. J.Cell Sci., 87: 667–675PubMedGoogle Scholar
  40. Owens, N.F., Gingell, D. & Trommler, A. (1988b) Cell adhesion to hydroxyl groups of a monolayer film. J.Cell Sci., 91: 269–279PubMedGoogle Scholar
  41. Painter, R.G. & Ginsberg, M. (1982) Concanavalin A induces interactions between surface glycoproteins and the platelet cytoskeleton. J.Cell Biol., 92: 565–573PubMedCrossRefGoogle Scholar
  42. Parsegian, V.A. & Gingell, D. (1973) A physical force model of biological membrane interaction. In: Recent advances in adhesion. Editor, L.H.Lee. Gordon & Breach Science Publishers, Inc., New York, pp 153–192Google Scholar
  43. Parsegian, V.A. & Gingell, D. (1980) Red blood cell adhesion. 111. Analysis of forces. J.Cell Sci., 41: 151–157PubMedGoogle Scholar
  44. Parsegian, V.A., Rand, R.P., Fuller, N. & Rau, D.C. (1979) Osmotic stress for the direct measurement of intermolecular forces. Methods in Enzymology, 127: 400–416CrossRefGoogle Scholar
  45. Ruckenstein, E. & Gourisankar, S.V. (1984) A surface energetic criterion of blood compatibility to foreign surfaces. J.Coll. Interface. Sci., 101: 436–451CrossRefGoogle Scholar
  46. Sa da Costa, V., Brier-Russell, D., Trudel, G., Waugh, D.F., Salzman, E.W. & Merrill, E.W. (1980) Polyether-polyurethane surfaces: thrombin adsorption, platelet adsorption and ESCA scanning. J.Coll. Interface Sci. 76: 594–596CrossRefGoogle Scholar
  47. Sa da Costa, V., Brier-Russell, D., Salzman, E.W. & Merrill, E.W. (1981) ESCA studies on polyurethanes: blood platelet activation in relation to surface composition. J.Coll. Interface Sci., 80: 445–452CrossRefGoogle Scholar
  48. Sheterline, P. & Hopkins, C.R. (1981) Transmembrane linkage between surface glycoproteins and components of the cytoplasm in neutrophil leukocytes. J.Cell Biol., 90: 743–754PubMedCrossRefGoogle Scholar
  49. Sheterline, P., Rickard, J.E. & Richards, R.C. (1984) Fc receptor-directed phagocytic stimuli induce transient actin assembly at an early stage of phagocytosis in neutrophil leukocytes. Eur.J Cell Biol., 34: 80–87PubMedGoogle Scholar
  50. Todd, I. & Gingell, D. (1980) Red blood cell adhesion. 1. Determination of the ionic conditions for adhesion to an oil-water interface. J.Cell Sci., 41: 125–133PubMedGoogle Scholar
  51. Todd, I., Mellor, J.S. & Gingell, D. (1988) Mapping cell-glass contacts of Dictyostelium amoebae by total internal reflection aqueous fluorescence overcomes a basic ambiguity of interference reflection microscopy. J.Cell Sci., 89: 107–114PubMedGoogle Scholar
  52. Trommler, A., Gingell, D. & Woolf, H. (1985) Red blood cells experience electrostatic repulsion but make molecular adhesions with glass. Biophys.J., 48: 835–841PubMedCrossRefGoogle Scholar
  53. Wang, E., Michl, J., Pffeffer, L.M., Silverstein, S.C. & Tamm, I. (1984) Interferon suppresses pinocytosis but stimulates phagocytosis in mouse peritoneal macrophages: related changes in cytoskeletal organization. J.Cell Biol., 98: 1328–1341PubMedCrossRefGoogle Scholar
  54. Whicher, S.J. & Brash, J.L. (1978) Platelet-foreign surface interactions: release of granule constituents from adherent platelets. J.Biomed. Mat. Res., 12: 181–201CrossRefGoogle Scholar
  55. Verschueren, H. (1985) Interference reflection microscopy in cell biology: methodology and applications. J.Cell Sci., 75: 279–301PubMedGoogle Scholar

Copyright information

© Springer-Verlag Berlin Heidelberg 1990

Authors and Affiliations

  • David Gingell
    • 1
  1. 1.Department of Anatomy and Developmental BiologyUniversity College and Middlesex School of MedicineLondonUK

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