Transepithelial transport in cell culture:d-Glucose transport by a pig kidney cell line (LLC-PK1)
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Summary
The pig kidney cell line LLC-PK1 cultured on a collagen coated membrane filter formed a continuous sheet of oriented asymmetrical epithelial cells joined by occluding junctions. A transepithelial electrical potential (PD) and short-circuit current (SCC) were dependent on the presence of Na and sugar in the apical bathing solution. In the presence of 5.5mm d-glucose, a PD of 2.8 mV, apical surface negative, a SCC of 13 μA cm−2 and transepithelial resistance of 211 ohm·cm2 were recorded. The SCC was promptly reduced by the addition of phlorizin to the apical bath but unaffected when placed in the basolateral bath. The effect on SCC of various sugars was compared by the concentrations required for half-maximal SCC: 0.13mm β-methyl-d-glucoside, 0.28mm d-glucose, 0.65mm α-methyl-d-glucoside, 0.77mm 6-deoxy-d-glucose, 4.8mm d-galactose, and 29mm 3-O-methyl-glucose. When [Na] was reduced, the concentration ofd-glucose required for half-maximal SCC increased. Isotopically labeled3H and14Cd-glucose were used to simultaneously determine bidirectional fluxes; a resultant net apical-to-basolateral transport was present and abolished by phlorizin. The transported isotope cochromatographed with labeledd-glucose, indicating negligible metabolism of transported glucose. The pig kidney cell line, LLC-PK1, provides a cell culture model for the investigation of mechanisms of transepithelial glucose transport.
Key words
Hexoses short-circuit current transepithelial transport phlorizin sodium dependentPreview
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References
- Barry, R.J.C., Smyth, D.H., Wright, E.M. 1965. Short-circuit current and solute transfer by rat jejunum.J. Physiol. (London) 181:410Google Scholar
- Bisbee, C.A., Machen, T.E., Bern, H.A. 1979. Mouse mammary epithelial cells on floating collagen gels. Transepithelial ion transport and effect of prolactin.Proc. Natl. Acad. Sci. USA 76:536Google Scholar
- Burg, M., Patlak, C., Green, N., Villey, D. 1976. Organic solutes in fluid absorption by renal proximal convoluted tubules.Am. J. Physiol. 231:627Google Scholar
- Cereijido, M., Robbins, E.S., Dolan, W.J., Rotunno, C.A., Sabatini, D.D. 1978. Polarized monolayers formed by epithelial cells on a permeable and translucent support.J. Cell Biol. 77:853Google Scholar
- Chesney, R., Sacktor, B., Kleinzeller, A. 1974. The binding of phloridizin to the isolated luminal membrane of the renal proximal tubule.Biochim. Biophys. Acta 332:263Google Scholar
- Chinard, F.P., Taylor, W.R., Nolan, M.F., Enns, T. 1959. Renal handling of glucose in dogs.Am. J. Physiol. 196:535Google Scholar
- Cohen, J.J., Barac-Nieto, M. 1973. Renal metabolism of substrates in relation to renal function.In: Handbook of Physiology. Section 8: Renal Physiology. J. Orloff and R.W. Berliner, editors. p. 964. American Physiological Society, Washington, D.C.Google Scholar
- Crane, R.K. 1960. Intestinal absorption of sugar.Physiol. Rev. 40:789Google Scholar
- Fairclough, P., Malathi, H., Presier, H., Crane, R.K. 1979. Reconstitution into liposomes of glucose active transport from the rabbit renal proximal tubule. Characteristics of the system.Biochim. Biophys. Acta 553:295Google Scholar
- Frasch, W., Frohnert, P.P., Bode, F., Baumann, K., Kinne, R. 1970. Competitive inhibition of phlorizin binding byd-glucose and the influence of sodium: A study on isolated brush border membrane of rat kidney.Pflueger's Arch. 320:265Google Scholar
- Fromter, E. 1979. Solute transport across epithelia: What can we learn from micropuncture studies on kidney tubules?J. Physiol. (London) 288:1Google Scholar
- Hull, R.N., Cherry, W.R., Weaver, G.W. 1976. The origin and characteristics of a pig kidney cell strain LLC-PK1.In Vitro 12:670Google Scholar
- Kippen, I., Hirayama, B., Klinenberg, J.R., Wright, E.M. 1979. Transport of tricarboxylic acid cycle intermediates by membrane vesicles from renal brush border.Proc. Nat. Acad. Sci. USA 76:3397Google Scholar
- Leighton, J., Brada, Z., Estes, L.W., Justa, G. 1969. Secretory activities and oncogenicity of a cell line (MDCK) derived from a canine kidney.Science 163:472Google Scholar
- Misfeldt, D.S., Hamamoto, S.T., Pitelka, D.R. 1976. Transepithelial transport in cell culture.Proc. Nat. Acad. Sci. USA 73:1212Google Scholar
- Mullin, J.M., Diamond, L., Kleinzeller, A. 1979. Uptake of alpha-methyl-d-glucoside and 3-O-methyl-d-glucose by an established pig renal epithelial line.Fed. Proc. 38:1058Google Scholar
- Owens, R.B., Smith, H.S., Hacket, A.J. 1974. Epithelial cell culture from normal glandular tissue of mice.J. Nat. Cancer Inst. 53:261Google Scholar
- Pickett, P.B., Pitelka, D.R., Hamamoto, S.T., Misfeldt, D.S. 1975. Occluding junctions and cell behavior in primary cultures of normal and neoplastic mammary-gland cells.J. Cell Biol. 66:316Google Scholar
- Puck, T.T. 1972. The Mammalian Cell as a Microorganism. Holden-Day, San FranciscoGoogle Scholar
- Rabito, C.A., Ausiello, D.A. 1980. Na+-dependent sugar transport in a cultured epithelial cell line from pig kidney.J. Membrane Biol. 54:31Google Scholar
- Schultz, S.G., Zalusky, R. 1964. Ion transport in isolated rabbit ileum. I. Short-circuit current and Na fluxes.J. Gen. Physiol. 47:567Google Scholar
- Taub, M., Chuman, L., Saier, M.H., Sato, G.H. 1979. The growth of a kidney epithelial cell line (MDCK) in hormone-supplemented serum-free media.Proc. Nat. Acad. Sci. USA 76:3338Google Scholar
- Tune, B.M., Burg, M.B. 1971. Glucose transport by proximal renal tubule.Am. J. Physiol. 221:580Google Scholar
- Turner, R.J., Silverman, M. 1978. Sugar uptake into brush border vesicles from dog kidney. II. Kinetics.Biochim. Biophys. Acta 511:470Google Scholar
- Ullrich, K.J. 1979. Sugar, Amino acid and Na cotransport in proximal tubule.Ann. Rev. Physiol. 41:181Google Scholar
- Ullrich, K.J., Rumrich, G., Kloss, S. 1974. Specificity and sodium dependence of the active sugar transport in the proximal convolution of the rat kidney.Pfluegers Arch. 351:35Google Scholar