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Activation of amino acid diffusion by a volume increase in cultured kidney (MDCK) cells

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Summary

When MDCK cells are cultured in MEM, they maintain a high concentration of three amino acids: glutamate (25mm), taurine (19 mm) and glycine (9 mm). With incubation of the cells in hypotonic media, the contents of these amino acids measured by HPLC are reduced in different time courses: taurine decreases most rapidly, followed by glutamate and glycine. All these losses are Na+ independent. To determine the transport mechanism activated by the hypotonic media, increasing external concentrations reaching 60 mm for nine different amino acids in Na+-free media were tested separately. For the five neutral (zwitterionic) amino acids, taurine, glycine, alanine, phenylalanine and tryptophan, cell contents increased linearly with external concentrations in hypotonic media, whereas in isotonic media only a slight rise was observed. The two anionic amino acids, glutamate and aspartate, were also increased linearly with their external concentrations in hypotonic media, but the changes were lower than those found for neutral amino acids. The presence of a negative membrane potential was responsible for this behavior since, using a K+ hypotonic medium which clamps the potential to zero, the glutamate content was found to increase linearly with an amplitude similar to the one observed for neutral amino acid. When external concentrations of two cationic amino acids, arginine and lysine, were increased in hypotonic media, only a small change, similar to that in isotonic media, was observed. These results indicate that a diffusion process for neutral and anionic amino acids is activated by a volume increase and it is suggested that an anion channel is involved.

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References

  1. Banderali, U., Roy, G. 1991. Ionic conductances activated during volume regulation in MDCK cells: a patch clamp study. Biophys. J. 59, 254a

    Google Scholar 

  2. Banderali, U., Roy, G. 1992. Activation of K+ and Cl channels in MDCK cells during volume regulation in hypotonic media. J. Membrane Biol. 126:219–234

    Google Scholar 

  3. Boerner, P., Evans-Layng, M., Sang, H., Saier, M.H. Jr. 1986. Polarity of neutral amino acid transport and characterization of a broad specificity transport activity in a kidney epithelial cell line, MDCK. J. Biol. Chem. 261:13957–13962

    Google Scholar 

  4. Brunner, J., Graham, D.E., Hauser, H., Semenza, G. 1980. Ion and sugar permeabilities of lecithin bilayers: comparison of curved and planar bilayers. J. Membrane Biol. 57:133–141

    Google Scholar 

  5. Chamberlain, M.E., Strange, K. 1989. Anisosmotic cell volume regulation: a comparative review. Am. J. Physiol. 257:C159-C173

    Google Scholar 

  6. Garcia-Perez, A., Burg, M.B. 1991. Role of organic osmolytes in adaptation of renal cells to high osmolality. J. Membrane Biol. 119:1–13.

    Google Scholar 

  7. Gilles, R. 1979. Intercellular organic osmotic effectors. In: Mechanism of Osmoregulation in Animals: Maintenance of Cell Volume. R. Gilles, editor. pp. 111–154. New York, John Wiley & Sons.

    Google Scholar 

  8. Haussinger, D., Lang, F. 1989. Exposure of perfused liver to hypotonic conditions modifies cellular nitrogen metabolism. J. Cell. Biochem. 43:355–361

    Google Scholar 

  9. Hoffmann, E.K., Lambert, I.H. 1983. Amino acid transport and cell volume regulation in Ehrlich ascites tumor cells. J. Physiol. 338:613–625

    Google Scholar 

  10. Jones, D.P., Miller, L.A., Russell, W.C. 1990. Adaptive regulation of taurine transport in two continuous renal epithelial cell lines. Kidney Int. 38:219–226

    Google Scholar 

  11. Jones, B.N., Gilligan, J.P. 1983. o-Phthaldialdehyde precolumn derivatization and reverse-phase high performance liquid chromatography of polypeptide hydrolysates and physiological fluids. J. Chromatogr. 266:471–482

    Google Scholar 

  12. Roy, G., Sauvé, R. 1987. Effect of anisotonic media on volume, ion and amino-acid content and membrane potential of kidney cells (MDCK) in culture. J. Membrane Biol. 100:83–96

    Google Scholar 

  13. Sanchez-Olea, R., Moran, J. Shousboe, A., PasantesMorales, H. 1991. Hyposmolarity-activated fluxes of taurine in astrocytes are mediated by diffusion. Neurosci. Lett. 130:233–236

    Google Scholar 

  14. Sanchez-Olea, R., Pasantes-Morales, H., Lazaro, A., Cereijido, M. 1991. Osmolarity-sensitive release of free amino acids from cultured kidney cells (MDCK). J. Membrane Biol. 121:1–9

    Google Scholar 

  15. Semenza, G., Corcelli, A. 1986. The absorption of sugars and amino acids across the small intestine. In: Molecular and Cellular Basis of Digestion. P. Denuelle, editor. pp. 381–412. Amsterdam, Elsevier

    Google Scholar 

  16. Siebenz, A.W., Spring, K.R. 1989. A novel sorbitol transport mechanism in cultured renal papillary epithelial cells. Am. J. Physiol. 257:F937-F946

    Google Scholar 

  17. Stevens, B.R., Kaunitz, J.D., Wright, E.M. 1984. Intestinal transport of amino acids and sugars: Advances using membrane vesicles. Annu. Rev. Physiol. 46:417–433

    Google Scholar 

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Roy, G., Malo, C. Activation of amino acid diffusion by a volume increase in cultured kidney (MDCK) cells. J. Membarin Biol. 130, 83–90 (1992). https://doi.org/10.1007/BF00233740

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  • DOI: https://doi.org/10.1007/BF00233740

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