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Improvements in the method for the electron microscopic localization of arylsulphatase activity

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Summary

The optimal conditions for the demonstration of arylsulphatase activity in the proximal convoluted tubule cells of the rat kidney were studied at light and electron microscopic level. 8-hydroxyquinoline sulphate, p-nitrophenyl sulphate and 2-hydroxy-5-nitrophenylsulphate were used as substrates and barium and lead as capturing ions. The effect of fixation, capturing ions, substrate concentration and pH was studied biochemically. The results of these biochemical studies were then verified histochemically. Finally a recommended method for the light and electron microscopic demonstration of arylsulphatase activity was presented.

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References

  • Behnke, O.: Nonspecific deposition of lead in experiments on fine structural localization of enzymatic activity of rat blood platelets. J. Histochem. Cytochem. 14, 432–433 (1966).

    Google Scholar 

  • Dodgson, K. S., B. Spencer and J. Thomas: Studies on sulphatases 9. The arylsulphatases of mammalian livers. Biochem. J. 59, 29–37 (1955).

    Google Scholar 

  • De Duve, C., R. Wattiaux and P. Baudhuin: Distribution of enzymes between subcellular fractions in animal tissues. Advanc. Enzymol. 24, 291–358 (1962).

    Google Scholar 

  • Ericsson, J. L. E., and B.F. Trump: Observations on the application to electron microscopy of the lead phosphate technique for the demonstration of acid phosphatase. Histochemie 4, 470–487 (1965).

    Google Scholar 

  • Goldfischer, S.: The cytochemical demonstration of lysosomal aryl sulfatase activity by light and electron microscopy. J. Histochem. Cytochem. 13, 520–524 (1965).

    Google Scholar 

  • Hopsu, V. K., A. Arstila, and G. G. Glenner: A method for electron microscopic localization of aryl-sulphatase. Ann. Med. exp. Fenn. 43, 114–116 (1965a).

    Google Scholar 

  • : The electron microscopic localization of aryl-sulphatase activity. J. Histochem. Cytochem. 13, 711–712 (1965b).

    Google Scholar 

  • - -H. Helminen: Studies on the electron microscopy of arylsulphatase and carbonic anhydrase activies. Abstract of the paper presented in Internat. Symposium. Electron Microscopy and Cytochemistry. Leiden 1966. J. Histochem. Cytochem. (in press).

  • Karlsson, U, and R.C. Schultz: Fixation of the central nervous system for electron microscopy by aldehyde perfusion. J. Ultrastruct. Res. 12, 160–186 (1965).

    Google Scholar 

  • Reynolds, E. S.: The use of lead citrate as an electron dense stain in electron microscopy. J. Cell Biol. 17, 208–212 (1963).

    Google Scholar 

  • Robinson, D., J.N. Smith, and R.T. Williams: Colorimetric determination of arylsulphatase Biochem. J. 49, 1 xxiv (1951).

    Google Scholar 

  • Sabatini, D.D., K. Bensch, and R.J. Barrnett: Cytochemistry and electron microscopy. The preservation of cellular ultrastructure and enzymatic activity by aldehyde fixation. J. Cell Biol. 17, 19–58 (1963).

    Google Scholar 

  • Torack, R.M.: The extracellular space of rat brain following perfusion fixation with glutaraldehyde and hydroxyadipaldehyde. Z. Zellforsch. 66, 352–364 (1965).

    Google Scholar 

  • Watson, M.L.: Staining of tissue sections for electron microscopy with heavy metals. J. biophys. biochem. Cytol. 4, 475–478 (1958).

    Google Scholar 

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Hopsu-Havu, V.K., Arstila, A.U., Helminen, H.J. et al. Improvements in the method for the electron microscopic localization of arylsulphatase activity. Histochemie 8, 54–64 (1966). https://doi.org/10.1007/BF00279874

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  • DOI: https://doi.org/10.1007/BF00279874

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