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. 1980 Jan 15;186(1):59–69. doi: 10.1042/bj1860059

Subcellular distribution and movement of 5'-nucleotidase in rat cells.

K K Stanley, M R Edwards, J P Luzio
PMCID: PMC1161503  PMID: 6245642

Abstract

1. Cell-surface 5'-nucleotidase was assayed by incubating whole-cell suspensions with 5'[3H]-AMP in iso-osmotic buffer and measuring [3H]adenosine production. The activity of cell-surface 5'-nucleotidase in hepatocytes, adipocytes and lymphocytes isolated from the rat was 15.0, 0.5 and 0.8pmol/min per cell at 37 degrees C respectively. 2. Disruption of the cells by vigorous mechanical homogenization or detergent treatment exposed additional 5'-nucleotidase activity, which represented 52%, 25% and 21% of the total activity in the three cell types respectively. This increase in 5'-nucleotidase activity which occurred when the cells were homogenized was due to a second pool of 5'-nucleotidase within the cell, rather than activation of the cell-surface enzyme. 3. In hepatocytes the intracellular 5'-nucleotidase activity was membrane-bound, indistinguishable from cell-surface 5'-nucleotidase in its inhibition by rabbit anti-(rat liver 5'-nucleotidase) serum and its kinetics with AMP, and was located on the extracytoplasmic face of vesicles within the cell. 4. The cell-surface 5'-nucleotidase of rat hepatocytes was rapidly inhibited when rabbit anti-(rat liver 5'-nucleotidase) serum or concanavalin A was added to the medium at 37 degrees C. Incubation with antiserum for 5 min at 37 degrees C inhibited 83 +/- 3% of the cell-surface enzyme. 5. Incubation of hepatocytes with exogenous antiserum or concanavalin A for 30 min at 37 degrees C resulted in over 50% inhibition of the intracellular enzyme. This inhibition was not prevented by disruption of the cytoskeleton or by ATP depletion. 6. Incubation of hepatocytes with exogenous antiserum or concanavalin A for up to 2h at 0 degrees C caused little or no inhibition of the intracellular enzyme, but over 75% inhibition of the cell-surface enzyme. 7. When surface-inhibited hepatocytes were washed and resuspended in buffer at 37 degrees C, 5'-nucleotidase was observed to redistribute from the intracellular pool to the cell surface.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Abercrombie M., Heaysman J. E., Pegrum S. M. The locomotion of fibroblasts in culture. 3. Movements of particles on the dorsal surface of the leading lamella. Exp Cell Res. 1970 Oct;62(2):389–398. doi: 10.1016/0014-4827(70)90570-7. [DOI] [PubMed] [Google Scholar]
  2. Anderson F. S., Murphy R. C. Isocratic separation of some purine nucleotide, nucleoside, and base metabolites from biological extracts by high-performance liquid chromatography. J Chromatogr. 1976 Jun 23;121(2):251–262. doi: 10.1016/s0021-9673(00)85021-9. [DOI] [PubMed] [Google Scholar]
  3. Arion W. J., Wallin B. K., Lange A. J., Ballas L. M. On the involvement of a glucose 6-phosphate transport system in the function of microsomal glucose 6-phosphatase. Mol Cell Biochem. 1975 Feb 28;6(2):75–83. doi: 10.1007/BF01732001. [DOI] [PubMed] [Google Scholar]
  4. Avruch J., Wallach D. F. Preparation and properties of plasma membrane and endoplasmic reticulum fragments from isolated rat fat cells. Biochim Biophys Acta. 1971 Apr 13;233(2):334–347. doi: 10.1016/0005-2736(71)90331-2. [DOI] [PubMed] [Google Scholar]
  5. Ballas L. M., Arion W. J. Measurement of glucose 6-phosphate penetration into liver microsomes. Confirmation of substrate transport in the glucose-6-phosphatase system. J Biol Chem. 1977 Dec 10;252(23):8512–8518. [PubMed] [Google Scholar]
  6. Bergeron J. J., Sikstrom R., Hand A. R., Posner B. I. Binding and uptake of 125I-insulin into rat liver hepatocytes and endothelium. An in vivo radioautographic study. J Cell Biol. 1979 Feb;80(2):427–443. doi: 10.1083/jcb.80.2.427. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Berry M. N., Friend D. S. High-yield preparation of isolated rat liver parenchymal cells: a biochemical and fine structural study. J Cell Biol. 1969 Dec;43(3):506–520. doi: 10.1083/jcb.43.3.506. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Bretscher M. S. Directed lipid flow in cell membranes. Nature. 1976 Mar 4;260(5546):21–23. doi: 10.1038/260021a0. [DOI] [PubMed] [Google Scholar]
  9. Conn P. M., Conti M., Harwood J. P., Dufau M. L., Catt K. J. Internalisation of gonadotrophin--receptor complex in ovarian luteal cells. Nature. 1978 Aug 10;274(5671):598–600. doi: 10.1038/274598a0. [DOI] [PubMed] [Google Scholar]
  10. DePierre J. W., Karnovsky M. L. Ecto-enzymes of the guinea pig polymorphonuclear leukocyte. I. Evidence for an ecto-adenosine monophosphatase, adenosine triphosphatase, and -p-nitrophenyl phosphates. J Biol Chem. 1974 Nov 25;249(22):7111–7120. [PubMed] [Google Scholar]
  11. DePierre J. W., Karnovsky M. L. Plasma membranes of mammalian cells: a review of methods for their characterization and isolation. J Cell Biol. 1973 Feb;56(2):275–303. doi: 10.1083/jcb.56.2.275. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Dipple I., Elliott K. R., Houslay M. D. Detergents modify the form of Arrhenius plots of 5'-nucleotidase activity. FEBS Lett. 1978 May 1;89(1):153–156. doi: 10.1016/0014-5793(78)80543-2. [DOI] [PubMed] [Google Scholar]
  13. Doyle D., Baumann H., England B., Friedman E., Hou E., Tweto J. Biogenesis of plasma membrane glycoproteins in hepatoma tissue culture cells. J Biol Chem. 1978 Feb 10;253(3):965–973. [PubMed] [Google Scholar]
  14. EMMELOT P., BOS C. J., BENEDETTI E. L., RUEMKE P. STUDIES ON PLASMA MEMBRANES. I. CHEMICAL COMPOSITION AND ENZYME CONTENT OF PLASMA MEMBRANES ISOLATED FROM RAT LIVER. Biochim Biophys Acta. 1964 Jul 15;90:126–145. doi: 10.1016/0304-4165(64)90125-4. [DOI] [PubMed] [Google Scholar]
  15. Farquhar M. G., Bergeron J. J., Palade G. E. Cytochemistry of Golgi fractions prepared from rat liver. J Cell Biol. 1974 Jan;60(1):8–25. doi: 10.1083/jcb.60.1.8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Fritzson P. 5'-Nucleotidase activities in the soluble fraction of rat liver. Biochim Biophys Acta. 1968 Mar 25;151(3):716–718. doi: 10.1016/0005-2744(68)90029-6. [DOI] [PubMed] [Google Scholar]
  17. Fritzson P. Nucleotidase activities in the soluble fraction of rat liver homogenate. Partial purification and properties of a 5'-nucleotidase with pH optimum 6.3. Biochim Biophys Acta. 1969 May 27;178(3):534–541. doi: 10.1016/0005-2744(69)90222-8. [DOI] [PubMed] [Google Scholar]
  18. Gold G., Widnell C. C. Relationship between microsomal membrane permeability and the inhibition of hepatic glucose-6-phosphatase by pyridoxal phosphate. J Biol Chem. 1976 Feb 25;251(4):1035–1041. [PubMed] [Google Scholar]
  19. Gurd J. W., Evans W. H. Distribution of liver plasma membrane 5' nucleotidase as indicated by its reaction with anti-plasma membrane serum. Arch Biochem Biophys. 1974 Sep;164(1):305–311. doi: 10.1016/0003-9861(74)90035-6. [DOI] [PubMed] [Google Scholar]
  20. Hales C. N. Immunological techniques in diabetes research. Diabetologia. 1972 Aug;8(4):229–235. doi: 10.1007/BF01225565. [DOI] [PubMed] [Google Scholar]
  21. Jackson G. D., Lemaître-Coelho I., Vaerman J. P., Bazin H., Beckers A. Rapid disappearance from serum of intravenously injected rat myeloma IgA and its secretion into bile. Eur J Immunol. 1978 Feb;8(2):123–126. doi: 10.1002/eji.1830080210. [DOI] [PubMed] [Google Scholar]
  22. Kitcher S. A., Siddle K., Luzio J. P. A method for the determination of glucose-6-phosphatase activity in rat liver with [U-14C]glucose 6-phosphate as substrate. Anal Biochem. 1978 Jul 15;88(1):29–36. doi: 10.1016/0003-2697(78)90395-0. [DOI] [PubMed] [Google Scholar]
  23. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  24. Luzio J. P., Newby A. C., Hales C. N. A rapid immunological procedure for the isolation of hormonally sensitive rat fat-cell plasma membrane. Biochem J. 1976 Jan 15;154(1):11–21. doi: 10.1042/bj1540011. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Nakamura S. Effect of sodium deoxycholate on 5'-nucleotidase. Biochim Biophys Acta. 1976 Mar 5;426(2):339–347. doi: 10.1016/0005-2736(76)90343-6. [DOI] [PubMed] [Google Scholar]
  26. Neville D. M., Jr Molecular weight determination of protein-dodecyl sulfate complexes by gel electrophoresis in a discontinuous buffer system. J Biol Chem. 1971 Oct 25;246(20):6328–6334. [PubMed] [Google Scholar]
  27. Newby A. C., Luzio J. P., Hales C. N. The properties and extracellular location of 5'-nucleotidase of the rat fat-cell plasma membrane. Biochem J. 1975 Mar;146(3):625–633. doi: 10.1042/bj1460625. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Newby A. C. The role of 5'-nucleotidase [proceedings]. Biochem Soc Trans. 1979 Oct;7(5):1030–1031. doi: 10.1042/bst0071030a. [DOI] [PubMed] [Google Scholar]
  29. Nilsson O. S., Arion W. J., Depierre J. W., Dallner G., Ernster L. Evidence for the involvement of a glucose-6-phosphate carrier in microsomal glucose-6-phosphatase activity. Eur J Biochem. 1978 Jan 16;82(2):627–634. doi: 10.1111/j.1432-1033.1978.tb12059.x. [DOI] [PubMed] [Google Scholar]
  30. Orlans E., Peppard J., Reynolds J., Hall J. Rapid active transport of immunoglobulin A from blood to bile. J Exp Med. 1978 Feb 1;147(2):588–592. doi: 10.1084/jem.147.2.588. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. PORTER R. R. The hydrolysis of rabbit y-globulin and antibodies with crystalline papain. Biochem J. 1959 Sep;73:119–126. doi: 10.1042/bj0730119. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. RODBELL M. METABOLISM OF ISOLATED FAT CELLS. I. EFFECTS OF HORMONES ON GLUCOSE METABOLISM AND LIPOLYSIS. J Biol Chem. 1964 Feb;239:375–380. [PubMed] [Google Scholar]
  33. ROY A. B. The sulphatase of ox liver. I. The complex nature of the enzyme. Biochem J. 1953 Jan;53(1):12–15. doi: 10.1042/bj0530012. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Recommended methods for the determination of four enzymes in blood. Scand J Clin Lab Invest. 1974 Jun;33(4):291–306. doi: 10.1080/00365517409082499. [DOI] [PubMed] [Google Scholar]
  35. Rider C. C., Taylor C. B. Enolase isoenzymes in rat tissues. Electrophoretic, chromatographic, immunological and kinetic properties. Biochim Biophys Acta. 1974 Sep 13;365(1):285–300. doi: 10.1016/0005-2795(74)90273-6. [DOI] [PubMed] [Google Scholar]
  36. Roth J. Compensatory membrane biogenesis and exocytosis as a result of concanavalin A-induced membrane internalization. Exp Cell Res. 1978 Jun;114(1):31–38. doi: 10.1016/0014-4827(78)90032-0. [DOI] [PubMed] [Google Scholar]
  37. SHONK C. E., BOXER G. E. ENZYME PATTERNS IN HUMAN TISSUES. I. METHODS FOR THE DETERMINATION OF GLYCOLYTIC ENZYMES. Cancer Res. 1964 May;24:709–721. [PubMed] [Google Scholar]
  38. Shaffer B. M. Mechanical control of the manufacture and resorption of cell surface in collective amoebae. J Theor Biol. 1965 Jan;8(1):27–40. doi: 10.1016/0022-5193(65)90089-5. [DOI] [PubMed] [Google Scholar]
  39. Stanley K. K., Edwards M. R., Luzio J. P. Rapid internalization of plasma-membrane 5'-nucleotidase in rat spleen lymphocytes in response to rabbit anti-(rat liver 5'-nucleotidase) serum [proceedings]. Biochem Soc Trans. 1979 Oct;7(5):1023–1024. doi: 10.1042/bst0071023. [DOI] [PubMed] [Google Scholar]
  40. Stanley K. K., Luzio J. P. The subcellular distribution of 5'-nucleotidase in isolated fat-cells and liver cells from rat [proceedings]. Biochem Soc Trans. 1979 Apr;7(2):361–362. doi: 10.1042/bst0070361. [DOI] [PubMed] [Google Scholar]
  41. Steinman R. M., Brodie S. E., Cohn Z. A. Membrane flow during pinocytosis. A stereologic analysis. J Cell Biol. 1976 Mar;68(3):665–687. doi: 10.1083/jcb.68.3.665. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Tanabe T., Pricer W. E., Jr, Ashwell G. Subcellular membrane topology and turnover of a rat hepatic binding protein specific for asialoglycoproteins. J Biol Chem. 1979 Feb 25;254(4):1038–1043. [PubMed] [Google Scholar]
  43. Trams E. G., Lauter C. J. On the sidedness of plasma membrane enzymes. Biochim Biophys Acta. 1974 Apr 29;345(2):180–197. doi: 10.1016/0005-2736(74)90257-0. [DOI] [PubMed] [Google Scholar]
  44. Tulkens P., Schneider Y. J., Trouet A. The fate of the plasma membrane during endocytosis. Biochem Soc Trans. 1977;5(6):1809–1815. doi: 10.1042/bst0051809. [DOI] [PubMed] [Google Scholar]
  45. Uusitalo R. J., Karnovsky M. J. Surface localization of 5'-nucleotidase on the mouse lymphocyte. J Histochem Cytochem. 1977 Feb;25(2):87–96. doi: 10.1177/25.2.14210. [DOI] [PubMed] [Google Scholar]
  46. Varga J. M., Moellmann G., Fritsch P., Godawska E., Lerner A. B. Association of cell surface receptors for melanotropin with the Golgi region in mouse melanoma cells. Proc Natl Acad Sci U S A. 1976 Feb;73(2):559–562. doi: 10.1073/pnas.73.2.559. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Westwood S. A., Luzio J. P., Flockhart D. A., Siddle K. Investigation of the subcellular distribution of cyclic-AMP phosphodiesterase in rat hepatocytes, using a rapid immunological procedure for the isolation of plasma membrane. Biochim Biophys Acta. 1979 Apr 3;583(4):454–466. doi: 10.1016/0304-4165(79)90062-x. [DOI] [PubMed] [Google Scholar]
  48. Widnell C. C. Cytochemical localization of 5'-nucleotidase in subcellular fractions isolated from rat liver. I. The origin of 5'-nucleotidase activity in microsomes. J Cell Biol. 1972 Mar;52(3):542–558. doi: 10.1083/jcb.52.3.542. [DOI] [PMC free article] [PubMed] [Google Scholar]
  49. Widnell C. C. Purification of rat liver 5'-nucleotidase as a complex with sphingomyelin. Methods Enzymol. 1974;32:368–374. doi: 10.1016/0076-6879(74)32037-x. [DOI] [PubMed] [Google Scholar]
  50. Wisher M. H., Evans W. H. Preparation of plasma-membrane subfractions from isolated rat hepatocytes. Biochem J. 1977 May 15;164(2):415–422. doi: 10.1042/bj1640415. [DOI] [PMC free article] [PubMed] [Google Scholar]
  51. el-Aaser A. A., Fitzsimons J. T., Hinton R. H., Norris K. A., Reid E. Electron microscopic examination of hepatic subcellular fractions for phosphatases. Histochem J. 1973 May;5(3):199–223. doi: 10.1007/BF01004989. [DOI] [PubMed] [Google Scholar]
  52. van den Berghe G., van Pottelsberghe C., Hers H. G. A kinetic study of the soluble 5'-nucleotidase of rat liver. Biochem J. 1977 Mar 15;162(3):611–616. doi: 10.1042/bj1620611. [DOI] [PMC free article] [PubMed] [Google Scholar]

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