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Autoradiography-based cytochemical detection of ecto-ATPase, ecto-ADPase, 5′-nucleotidase, and extracellular adenosine production, employing 141Ce3+ as a capturing agent

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Summary

A method for the visualization of the ecto-nucleotidase enzyme activities present on the cell surface, employing 141Ce3+ as a capturing and labelling agent, is described. Phosphate ions precipitated at the cell surface can be detected by coating the cells with an autoradiographic emulsion, followed by light microscopical inspection of the formed silver grains. The activities of ecto-ATPase, ecto-ADPase and 5′-nucleotidase were detected by this approach in four different cell lines. Parallel biochemical measurements of the activities of the corresponding enzymes were carried out in order to validate, evaluate, and optimize the cytochemical detection. The finding that Ce3+ ions are inhibitory to ecto-ATPase provided evidence for the necessity of carefully establishing appropriate reaction conditions for the cytochemical determination of ecto-nucleotidases. The application of this method to the indirect detection of extracellular adenosine production from substrates like ATP has also been documented. It allows a cytochemical determination of adenosine formed through cascade nucleotide dephosphorylation. This newly described method is of high sensitivity and potentially of value for a variety of applications, including not only cytochemistry but also cell biology, and molecular biology studies.

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References

  • Broekman, M. J., Eiroa, A. M. & Marcus, A. J. (1991) Inhibition of human platelet reactivity by endothelium-derived relaxing factor from human umbilical vein endothelial cells in suspension: blockade of aggregation and secretion by an aspirin-insensitive mechanism. Blood 78, 1033–10.

    Google Scholar 

  • Cheung, P. H., Thompson, N. L., Earley, K., Culic, O., Hixson, D. & Lin, S-H. (1993) Cell-CAM 105 isoforms with different adhesion functions are coexpressed in adult rat tissues and during liver development. J. Biol. Chem. 268, 6139–46.

    Google Scholar 

  • Culic, O., Sabolic, I. & Zanic-Grubisic, T. (1990) The stepwise hydrolysis of adenine nucleotides by ectoenzymes of rat renal brush-border membranes. Biochim. Biophys. Acta 1030, 143–51.

    Google Scholar 

  • Culic, O., Huang, Q-H., Flanagan, D., Hixson, D. & Lin, S-H. (1992) Molecular cloning and expression of a new rat liver cell-CAM105 isoform. Biochem. J. 285, 47–53.

    Google Scholar 

  • Dhalla, N. S. & Zhao, D. (1988) Cell membrane Ca2+/ Mg2+ ATPase. Prog. Biophys. Biol. 52, 1–37.

    Google Scholar 

  • Ethier, M. F., Chander, V. & Dobson, J. G. (1993) Adenosine stimulates proliferation of human endothelial cells in culture. Am. J. Physiol. 265, H131–8.

    Google Scholar 

  • Firth, J. A. (1978) Cytochemical approaches to the localization of specific adenosine triphosphatases. Histochem. J. 10, 253–69.

    Google Scholar 

  • Gomori, G. (1952) Microscopic Histochemistry: Principles and practice. Chicago: University Press.

    Google Scholar 

  • Gordon J, L. (1986) Extracellular ATP: effects, sources and fate. Biochem. J. 233, 309–19.

    Google Scholar 

  • Halbhuber, K-J., Hulstaert, C. E., Feuerstein, H. & Zimmermann, N. (1994) Cerium as capturing agent in phosphatase and oxidase histochemistry. In Prog. Histochem. Cytochem. 28, 1–120.

    Google Scholar 

  • Hyppönen, S., Kohila, T. & Tähti, H. (1993) The effects of cadmium, lead and aluminium on neural cell membrane adenosinetriphosphatase activity. Neurosci. Res. Comm. 12, 77–84.

    Google Scholar 

  • Ilsbroux, I., Vanduffel, L., Teuchy, H. & DeCuyper, M. (1985) An azide-insensitive low-affinity ATPase stimulated by Ca2+ or Mg2+ in basal-lateral and brushborder membranes of kidney cortex. Eur Biochem. 151, 123–9.

    Google Scholar 

  • Knowles, A. F., Isler, R. E. & Reece, J. F. (1983) The common occurance of ATP diphosphohydrolase in mammalian plasma membranes. Biochem. Biophys. Acta 731, 88–96.

    Google Scholar 

  • Lebel, D., Poirrier, G. G. & Beaudoin, A. R. (1978) A convenient method for the ATPase assay. Anal. Biochem. 85, 86–9.

    Google Scholar 

  • Le Hir, M. & Dubach, U. C. (1988) An ATP-inhibited soluble 5′-nucleotidase of rat kidney. Am. J. Physiol. 254, F191–5.

    Google Scholar 

  • Lin, S-H. & Guidotti, G. (1989) Cloning and expression of a cDNA coding for a rat liver plasma membrane ecto-ATPase. J. Biol. Chem. 264, 14 408–14.

    Google Scholar 

  • Lin, S-H., Culic, O., Flanagan, D. & Hixson, D. C. (1991) Immunochemical characterization of two isoforms of rat liver ecto-ATPase that show an immunological and structural identity with a glycoprotein cell-adhesion molecule with Mr 105 000. Biochem. J. 278, 155–61.

    Google Scholar 

  • Misumi, Y., Ogata, S., Hirose, S. & Ikehara, Y. (1990) Primary structure of rat liver 5′-nucleotidase deduced from cDNA. Presence of the COOH-terminal hydrophobic domain for possible post-translational modification by glycophospholipid. J. Biol. Chem. 265, 2178–83.

    Google Scholar 

  • Murray, R. D. & Churchill, P. C. (1985) Concentration-dependency of the renal vascular and renin secretory responses to adenosine receptor agonists. J. Pharmacol. Exp. Ther. 232, 189–93.

    Google Scholar 

  • Poelstra, K., Heynen, E. R., Baller, J. F. W., Hardonk, M. J. & Bakker, W. W. (1992) Modulation of anti-Thyl nephritis in the rat by adenine nucleotides. Lab. Invest. 66, 555–63.

    Google Scholar 

  • Robinson, J. M. & Karnovsky, M. J. (1983) Ultrastructural localization of 5′-nucleotidase in guinea pig neutrophils based upon the use of cerium as capturing agent. J. Histochem. Cytochem. 31, 1190–6.

    Google Scholar 

  • Sabolic, I., Culic, O., Lin, S-H. & Brown, D. (1992) Localization of ecto-ATPase in rat kidney and isolated renal cortical membrane vesicles. Am. J. Physiol. 262, F217–28.

    Google Scholar 

  • Seals, J. R., Mcdonald, J. M., Bruns, D. & Jarett, L. (1978) A sensitive and precise isotopic assay of ATPase activity. Anal. Biochem. 90, 785–95.

    Google Scholar 

  • Sippel, C. J., Suchy, F. J., Ananthanarayanan, M. & Perlmutter, D. H. (1993) The rat liver ecto-ATPase is also a canalicular bile acid transport protein. J. Biol. Chem. 268, 2083–91.

    Google Scholar 

  • Stahl, W. L. & Baskin, D. G. (1990) Histochemistry of ATPases. J. Histochem. Cytochem. 38, 1099–122.

    Google Scholar 

  • Stiles, G. L. (1992) Adenosine receptors. J. Biol. Chem. 267, 6451–54.

    Google Scholar 

  • Stochaj, U. & Mannherz, H. G. (1992) Chicken gizzard 5′-nucleotidase functions as a binding protein for the laminin/nidogen complex. Eur. J. Cell. Biol. 59, 364–72.

    Google Scholar 

  • Suzuki, K., Furukawa, Y., Tamura, H., Ejiri, N., Suematsu, H., Taguchi, R., Nakamara, S., Suzuki, Y. & Ikezawa, H. (1993) Purification and cDNA cloning of bovine liver 5′-nucleotidase, a GPI-anchored protein, and its expression in COS cells. J. Biochem. 113, 607–13.

    Google Scholar 

  • Takizawa, T. & Robinson, J. M. (1993) Combined immunocytochemistry and enzyme cytochemistry on ultrathin cryosections -a new method. J. Histochem. Cytochem. 41, 1635–9.

    Google Scholar 

  • Thompson, J. D. & Nechay, B. R. (1981) Inhibition by metals of a canine renal calcium, magnesium activated adenosinetriphosphatase. J. Toxicol. Environ. Health 7, 901–9.

    Google Scholar 

  • VanErum, M., Lemmens, R., Berden, J., Teuchy, H. & Vanduffel, L. (1995) Identification and partial purification of (Ca2+ or Mg2+)-ATPase in renal brushborder membranes. Eur. J Biochem. 227, 150–60.

    Google Scholar 

  • VanNoorden, C. J. F. & Frederiks, W. M. (1993) Cerium methods for light and electron microscopical histochemistry. J. Microscopy 171, 3–16.

    Google Scholar 

  • Zimmermann, H. (1992) 5′-nucleotidase: molecular structure and functional aspects. Biochem. J. 285, 345–65.

    Google Scholar 

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Culic, O., Lemmens, R., Teuchy, H. et al. Autoradiography-based cytochemical detection of ecto-ATPase, ecto-ADPase, 5′-nucleotidase, and extracellular adenosine production, employing 141Ce3+ as a capturing agent. Histochem J 27, 555–564 (1995). https://doi.org/10.1007/BF00174328

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  • DOI: https://doi.org/10.1007/BF00174328

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