Abstract
Cells grown in monolayer culture offer a convenient system for binding and other experiments under conditions that preserve the complexity of the living state. Kinetics experiments, however, may be distorted by the time course of drug penetration into even so simple a “tissue” as the monolayer. The impediments include unstirred layers both above and between the cells, the congregation of receptors within the confined space between cells, and nonspecific binding to membrane components. The contributions of these factors were investigated in cultures of Chinese hamster ovary (CHO) cells either nontransfected or stably transfected with μ opioid receptors. The dissociation of [3H]naloxone was four times faster under displacement than under infinite dilution conditions, clearly demonstrating the “retention effect” of receptors confined in space. Even the penetration of this ligand between nontransfected cells showed salient delays with respect to diffusion into a slab, indicating that nonspecific, low-affinity binding to membrane components was arresting its progress. The optical sectioning capabilities of confocal microscopy demonstrated that the kinetics of two fluorescent antagonists depended on the vertical plane, providing direct evidence for slowed diffusion down a single cell depth. Modeling shows that kinetic errors increase with receptor density, forward rate constant, and the thickness of the unstirred layer.
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References
Porzig, H. (1982) Are there differences in the β-receptor-adenylate cyclase systems of fragmented membranes and living cells? Trends Pharmacol. Sci. 3, 75–78.
Toll, L. (1995) Intact cell binding and the relation to opioid activities in SH-SY5Y cells. J. Pharmacol. Exp. Ther. 273, 721–727.
Nicholson, C., Phillips, J. M., and Gardner-Medwin, A. R. (1979) Diffusion from an iontophoretic point source in the brain: role of tortuosity and volume fraction. Brain Res. 169, 580–584.
Nicholson, C., Chen, K. C., Hrabetova, S., and Tao, L. (2000) Diffusion of molecules in brain extracellular space: theory and experiment. Prog. Brain Res. 125, 129–154.
Chen, K. C., and Nicholson, C. (2000) Changes in brain cell shape create residual extracellular space volume and explain tortuosity behavior during osmotic challenge. Proc. Natl. Acad. Sci. U.S.A. 97, 8306–8311.
DeLisi, C. (1981) The effect of cell size and receptor density on ligand-receptor reaction rate constants. Mol. Immunol. 18, 507–511.
Abbott, A. J. and Nelsestuen, G. L. (1988) The collisional limit: an important consideration for membrane-associated enzymes and receptors. FASEB J. 2, 2858–2866.
Goldstein, B., and Dembo, M. (1995) Approximating the effects of diffusion on reversible reactions at the cell surface: ligand-receptor kinetics. Biophys. J. 68, 1222–1230.
Berg, J. C., and Purcell, E. M. (1977) Physics of chemoreception. Biophys. J. 20, 193–219.
DeLisi, C. (1980) The biophysics of ligand-receptor interactions. Q. Rev. Biophys. 13, 201–230.
Shoup, D., and Szabo, A. (1982) Role of diffusion in ligand binding to macromolecules and cell-bound receptors Biophys. J. 40, 33–39.
Zwanzig, R. (1990) Diffusion-controlled ligand binding to spheres partially covered by receptors: an effective medium treatment. Proc. Natl. Acad. Sci. U.S.A. 87, 5856–5857.
Dainty, J., and House, C. R. (1966) Unstirred layers in frog skin. J. Physiol. 182, 66–78.
Pedley, T. J. (1983) Calculation of unstirred layer thickness in membrane transport experiments: a survey. Q. Rev. Biophys. 16, 115–150.
Barry, P. H., and Diamond, J. M. (1984) Effects of unstirred layers on membrane phenomena. Physiol. Rev. 64, 763–872.
Silhavy, T. J., Szmelcman, S., Boos, W., and Schwartz, M. (1975) On the significance of the retention of ligand by protein. Proc. Natl. Acad. Sci. U.S.A. 72, 2120–2124.
Rademaker, B., Kramer, K., van Ingen, H., Kranendonk, M., and Timmerman, H. (1985) Non-specific binding of the fluorescent beta-adrenergic receptor probe alprenolol-NBD. J. Recept. Res. 5, 121–131.
Wurm, F. M. (1990) Integration, amplification and stability of plasmid sequences in CHO cell cultures. Biologicals 18, 159–164.
Spivak, C. E., and Beglan, C. L. (2004) Kinetics of β-funaltrexamine binding to wild-type and mutant μ-opioid receptors expressed in Chinese hamster ovary cells. Synapse 52, 123–135.
Krnjevic, K. and Mitchell, J. F. (1960) Diffusion of acetylcholine in agar gels and in the isolated rat diaphragm. J. Physiol. 153, 562–572.
Crank, J. (1975) The Mathematics of Diffusion. 2nd ed. Oxford University Press, New York.
Verkman, A. S., and Dix, J. A. (1984) Effect of unstirred layers on binding and reaction kinetics at a membrane surface. Anal. Biochem. 142, 109–116.
Cussler, E. L. (1997) Diffusion: Mass Transfer in Fluid Systems. Cambridge University Press, New York.
Bardell, R. L., Weigl, B. H., Kesler, N., Schulte, T.H., Hayenga, J., and Battrell, C. F. Microfluidic Disposables for Cellular and Chemical Detection-CFD Model Results and Fluidic Verification Experiments. SPIE BIOS 2001, San Jose, January 2001.
Winzek, C., and Baumgärtel, H. (1988) Staining kinetics in single cells. Part I. Influence of convective diffusion on the staining rate. Histochemistry 90, 73–77.
Rusakov, D. A., and Kullmann, D. M. (1998) Geometric and viscous components of the tortuosity of the extracellular space in the brain. Proc. Natl. Acad. Sci. U.S.A. 95, 8975–8980.
Yam, K. L., Anderson, D. K., and Buxbaum, R. E. (1988) Diffusion of small solutes in polymer-containing solutions. Science 241, 330–332.
Kean, E. L. (1968) Rapid, sensitive spectrophotometric method for quantitative determination of sulfatides. J. Lipid Res. 9, 319–327.
Alberts, B., Bray, D., Lewis, J., Raff, M., Roberts, K., and Watson, J. D. (1994) Molecular Biology of the Cell, Garland Publishing, New York, pp. 478–484.
Madsen, B. W., Beglan, C. L., and Spivak, C. E. (2000) Fluorescein-labeled naloxone binding to mu opioid receptors on live Chinese hamster ovary cells using confocal fluorescent microscopy. J. Neurosci. Methods 97, 123–131.
Emmerson, P. J., Archer, S., El-Hamouly, W., Mansour, A., Akil, H., and Medzihradsky, F. (1997) Synthesis and characterization of 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY)-labeled fluorescent ligands for the mu opioid receptor. Biochem. Pharmacol. 54, 1315–1322.
De Meyts, P, Bioanco, A. R., and Roth, J. (1976) Site-site interactions among insulin receptors. J. Biol. Chem. 251, 1877–1888.
Fischel, s. V., and Medzihradsky, F. (1981) Scatchard analysis of opiate receptor binding. Mol. Pharmacol. 20, 269–279.
Pochet, R., and Schmitt, H. (1979) Re-evaluation of the number of specific beta-adrenergic receptors on muscle cells. Nature 277, 58–60.
Loh, H. H., Cho, T. M., Wu, Y. C., and Way, E. L. (1974) Stereospecific binding of narcotics to brain cerebrosides. Life Sci. 14, 2231–2245.
Loh, H. H., Cho, T. M., Wu, Y. C., Harris, R. A., and Way, E. L. (1975) Opiate binding to cerebroside sulfate: a model system for opiate-receptor interaction. Life Sci. 16, 1811–1817.
Cho, T. M., Cho, J. S., and Loh, H. H. (1976) A model for opiate-receptor interactions: mechanism of opiate-cerebroside sulfate interaction. Life Sci. 18, 231–244.
Law, P. Y., Fischer, G., Loh, H. H., and Herz, A. (1979) Inhibition of specific opiate binding to synaptic membrane by cerebroside sulfatase. Biochem. Pharmacol. 28, 2557–2562.
Law, P. Y., Harris, R. A., Loh, H. H., and Way, E. L. (1978) Evidence for the involvement of cerebroside sulfate in opiate receptor binding: studies with Azure A and jimpy mutant mice. J. Pharmacol. Exp. Ther. 207, 458–468.
Craves, F. B., Zalc, B., Leybin, L., Baumann, N., and Loh, H. H. (1980) Antibodies to cerebroside sulfate inhibit the effects of morphine and beta-endorphin. Science 207, 75–76.
Loh, H. H., and Law, P. Y. (1980) The role of membrane lipids in receptor mechanisms. Annu. Rev. Pharmacol. Toxicol. 20, 201–234.
van de Lest, C. H., Versteeg, E. M., Veerkamp, J. H., and van Kuppevelt, T. H. (1994) Quantification and characterization of glycosaminoglycans at the nanogram level by a combined azure A-silver staining in agarose gels. Anal. Biochem. 221, 356–361.
Inoue, H., Seyama, Y., and Yamashita, S. (1986) Specific determination of arylsulfatase A activity. Experientia 42, 33–35.
Sarkadi, B., Attisano, L., Grinstein, S., Buchwald, M., and Rothstein, A. (1984) Volume regulation of Chinese hamster ovary cells in anisoosmotic media. Biochim. Biophys. Acta 774, 159–168.
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Spivak, C.E., Oz, M., Beglan, C.L. et al. Diffusion delays and unstirred layer effects at monolayer cultures of Chinese hamster ovary cells. Cell Biochem Biophys 45, 43–58 (2006). https://doi.org/10.1385/CBB:45:1:43
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DOI: https://doi.org/10.1385/CBB:45:1:43