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Induction of 2′,3′-cyclic nucleotide 3′-phosphohydrolase and morphological alterations in C6 glioma cells by dexamethasone, (3-butoxy-4-methoxybenzyl)-2-imidazolinone and prostaglandin E1

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Summary

Dexamethasone, R020-1724 and prostaglandin E1 all induced morphological alterations and increased the glial specific enzyme 2′,3′-cyclic nucleotide 3′-phosphohydrolase (CNP) in rat C6 glioma cells in culture. Morphological alterations consisted mainly in the development of astrocytelike changes. Increases in dexamethasone-induced CNP activity was time dependent. Dexamethasone reduced cell growth rate, depending on the concentration employed.

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References

  1. Zanetta, J. P., P. Benda, G. Gombos, and I. G. Morgan. 1972. The presence of 2′,3′-cyclic AMP 3′-phosphohydrolase in glial cells in tissue culture. J. Neurochem. 19: 881–883.

    Article  PubMed  CAS  Google Scholar 

  2. Nagata, Y., K. Mikoshiba, and Y. Tsukuda. 1974. Neuronal cell body enriched and glial cell enriched fractions from young and adult rat brains: preparation and morphological and biochemical properties. J. Neurochem. 22: 493–503.

    Article  PubMed  CAS  Google Scholar 

  3. Poduslo, S. E., and W. T. Norton. 1972. Isolation and some chemical properties of oligodendroglia from calf brain. J. Neurochem. 19: 727–736.

    Article  PubMed  CAS  Google Scholar 

  4. Kurihara, T., J. L. Nussbaum, and P. Mandel. 1970. 2′,3′-Cyclic nucleotide 3′-phosphohydrolase in brains of mutant mice with deficient myelination. J. Neurochem. 17: 993–997.

    Article  PubMed  CAS  Google Scholar 

  5. Fry, J. M., G. M. Lehrer, and M. B. Bornstein. 1973. Experimental inhibition of myelination in spinal cord tissue cultures: enzyme assays. J. Neurobiol. 4: 453–459.

    Article  PubMed  CAS  Google Scholar 

  6. Mathieu, J. M., P. Honegger, B. D. Trapp, S. R. Cohen, and H. DeF. Webster. 1978. Myelination in rat brain aggregating cell culture. Neuroscience 3: 565–572.

    Article  Google Scholar 

  7. Kurihara, T., and Y. Tsukuda. 1967. The regional and subcellular distribution of 2′,3′-cyclic nucleotide 3′-phosphohydrolase in the central nervous system. J. Neurochem. 14: 1167–1174.

    Article  PubMed  CAS  Google Scholar 

  8. Olafson, R. W., G. Drummond, and J. F. Lee. 1969. Studies on 2′,3′-cyclic nucleotide 3′-phosphohydrolase from brain. Can. J. Biochem. 47: 961–966.

    Article  PubMed  CAS  Google Scholar 

  9. Kurihara, T., and Y. Tsukuda. 1968. 2′,3′-Cyclic nucleotide 3′-phosphohydrolase in the developing chick brain and spinal cord. J. Neurochem. 15: 827–832.

    Article  CAS  PubMed  Google Scholar 

  10. Braun, P. E., and R. L. Barchi. 1972. 2′,3′-Cyclic nucleotide 3′-phosphohydrolase in the nervous system. Electrophoretic properties and developmental studies. Brain Res. 40: 437–444.

    Article  PubMed  CAS  Google Scholar 

  11. Banic, N. L., and A. N. Davison. 1969. Enzyme activity and composition of myelin and subcellular fractions in the developing rat brain. Biochem. J. 115: 1051–1062.

    Google Scholar 

  12. Matthieu, J. M., and P. Honegger, B. D. Trapp, S. R. Cohen, and H. Webster. 1978. Myelination in rat brain aggregating cell culture. Neuroscience 3: 565–572.

    Article  PubMed  CAS  Google Scholar 

  13. McMorris, F. A. 1977. Norepinephrine induces glial-specific enzyme activity in cultured plasma glioma cells. Proc. Natl. Acad. Sci. U.S.A. 74: 4501–4504.

    Article  PubMed  CAS  Google Scholar 

  14. Oey, J. 1975. Noradrenaline induces morphological alterations in nucleated and enucleated rat C6 glioma cells. Nature 257: 317–319.

    Article  PubMed  CAS  Google Scholar 

  15. Gilman, A. G., and M. Nirenberg. 1971. Effect of catecholamines on the adenosine 3′,5′-cyclic monophosphate concentrations of clonal satellite cells of neurons. Proc. Natl. Acad. Sci. U.S.A. 68: 2165–2168.

    Article  PubMed  CAS  Google Scholar 

  16. Schimmer, B. P. 1971. Effects of catecholamines and monovalent cations on adenylate cyclase activity in cultured glial tumor cells. Biochem. Biophys. Acta 252: 567–573.

    PubMed  CAS  Google Scholar 

  17. Sandquist, D., T. M. Williams, S. K. Sahu, and S. Kataoka. 1978. Morphological differentiation of a murine neuroblastoma clone in monolayer culture induced by dexamethasone. Exp. Cell. Res. 113: 375–381.

    Article  PubMed  CAS  Google Scholar 

  18. Brostom, M. A., C. Kon, D. R. Olson, and B. Breckenridge. 1974. Adenosine 3′,5′-monophosphate in glial tumor cells treated with glucocorticoids. Mol. Pharmacol. 10: 711–720.

    Google Scholar 

  19. De Vellis, J., J. F. McGinnis, G. A. M. Breen, P. Leveille, K. Bennett, and K. McCarthy. 1977. In: S. Fedoroff and L. Hertz (Eds.),Cell, Tissue and Organ Culture in Neurobiology. Academic Press, New York.

    Google Scholar 

  20. Kôrínková, P., and Z. Lodin. 1977. A transitional differentiation of glial cells of cultured corpus callosum caused by dibutyryl cyclic adenosine monophosphate. Neuroscience 2: 1103–1114.

    Article  Google Scholar 

  21. Edström, A., M. Kanje, and E. Walum. 1974. Effects of dibutyryl cyclic AMP and prostaglandin E1 on cultured human glioma cells. Exp. Cell. Res. 85: 217–223.

    Article  PubMed  Google Scholar 

  22. Lowry, O. M., J. J. Rosebrough, A. L. Farr, and R. J. Randall. 1951. Protein measurement with the folin phenol reagent. J. Biol. Chem. 193: 265–275.

    PubMed  CAS  Google Scholar 

  23. Mealy, J., T. Chen, and G. P. Shantz. 1971. Effects of dexamethasone and methyl prednisone on cell cultures of human glioblastomas. J. Neurosurg. 34: 324–334.

    Article  Google Scholar 

  24. Berliner, J. A., K. Bennett, and J. de Vellis. 1978. Effect of hydrocortisone on cell morphology in C6 cells. J. Cell Physiol. 94: 321–334.

    Article  PubMed  CAS  Google Scholar 

  25. Grasso, R. J., T. A. Tedesco, S. F. Wodzinski, and C. E. Johnson. 1978. Temporal relationships between DNA metabolism and the growth-inhibitory response produced by dexamethasone in rat glioma cell cultures. In Vitro 14: 625–630.

    Article  PubMed  CAS  Google Scholar 

  26. Greenham, L. W., T. J. Hill, C. A. Moss, and D. B. Peacock. 1974. Preparation of disaggregated mouse brain cultures and observations on early neurite and axon formation therein. Exp. Cell. Res. 84: 287–299.

    Article  PubMed  CAS  Google Scholar 

  27. Daniel, D. F., and G. Wolf. 1975. Incorporation of labelled glucosamine into glycoproteins by organ cultures of hamster trachea: adverse effects of HEPES buffer. Neurobiology 11: 347–353.

    CAS  Google Scholar 

  28. Prasad, K. N., S. K. Sahu, and P. K. Sinha. 1976. Cyclic nucleotides in the regulation of expression of differentiated functions in neuroblastoma cells.J. Natl. Cancer Inst. 57: 619–631.

    PubMed  CAS  Google Scholar 

  29. Volpe, J. J., K. Fuiimoto, J. C. Marsala, and H. C. Agrawal. 1975. Relation of C6 glial cells in culture to myelin. Biochem. J. 152: 701–703.

    PubMed  CAS  Google Scholar 

  30. Dawson, G., S. Kemp, A. C. Stoolmiller, and A. Dorfman. 1971. Biosynthesis of glycospingolipids by mouse neuroblastoma (NBHIA), rat glia (RGG), and human glia (CHB-4) in cell culture. Biochem. Biophys. Res. Commun. 44: 687–694.

    Article  PubMed  CAS  Google Scholar 

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This paper is supported in part by N.I.M.H. Research Grant AA02372. Dr. S. Kamath participated initially in this study.

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Waziri, R., Sahu, S.K. Induction of 2′,3′-cyclic nucleotide 3′-phosphohydrolase and morphological alterations in C6 glioma cells by dexamethasone, (3-butoxy-4-methoxybenzyl)-2-imidazolinone and prostaglandin E1 . In Vitro 16, 97–102 (1980). https://doi.org/10.1007/BF02831499

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  • DOI: https://doi.org/10.1007/BF02831499

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