Skip to main content
Log in

Morphological differentiation of neuroblastoma cells induced by dimethylsulfoxide

  • Published:
Neurophysiology Aims and scope

Abstract

Morphological features of neuroblastoma cells grown in culture in the presence of dimethylsulfoxode (DMSO) were studied. Morphological differentiation, expressed as the appearance of long axon-like processes (neurites), an increase in size of the cells, and inhibition of cell division, was observed in neuroblastoma cells of line C 1300, subline N-18-TG2A1, incubated in medium containing 1% DMSO. In the early stages of culture in normal growth medium the cells possess primary features of morphological differentiation. Quantitative criteria for the development of these features depending on duration of culture in modified medium were worked out. An increase in the total length of the neurites of cells differentiating under the influence of DMSO is a linear function of time. The rate of growth of the neurites is 20.0±3.0 µ/h. The area of cross-section of the soma of the differentiated cells is 6–7 times greater than the corresponding parameter in the control. An increase in the DMSO concentration in the culture medium (1.5 and 2.0%) does not induce rapid growth of the neurites or an increase in size of the cell soma, but it does block mitosis. Characteristics of morphological differentiation of neuroblastoma cells are compared with probable functional changes in these cells.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Literature cited

  1. T. Amano, E. Richelson, and M. Nirenberg, "Neurotransmitter synthesis by neuroblastoma clones," Proc. Natl. Acad. Sci. USA,69, No. 1, 258 (1972).

    PubMed  Google Scholar 

  2. M. P. Bear and F. H. Schneider, "The effect of medium pH on rate of growth, neurite formation and acetylcholine esterase activity in mouse neuroblastoma cells in culture," J. Cell. Physiol.,91, No. 1, 63 (1977).

    PubMed  Google Scholar 

  3. A. Blume, F. Gilbert, S. Wilson, et al., "Regulation of acetylcholine esterase in neuroblastoma cells," Proc. Natl. Acad. Sci. USA,67, No. 2, 768 (1970).

    Google Scholar 

  4. J. E. Bottenstein, "Differentiated properties of neuronal cell lines," in: Functionally Differentiated Cell Lines, Alan Liss, New York (1981), pp. 155–184.

    Google Scholar 

  5. M. C. Fishman and I. Spector, "Potassium current suppression by quinidine reveals additional calcium currents in neuroblastoma cells," Proc. Natl. Acad. Sci. USA,78, No. 8, 5245 (1981).

    PubMed  Google Scholar 

  6. P. Furmanski, D. J. Silverman, and M. Lubin, "Expression of differentiated functions in mouse neuroblastoma mediated by dibutyryl-cyclic adenosine monophosphate," Nature,233, No. 3, 413 (1971).

    PubMed  Google Scholar 

  7. A. J. Harris and M. J. Dennis, "Acetylcholine sensitivity and distribution of mouse neuroblastoma cells," Science,167, 1253 (1970).

    PubMed  Google Scholar 

  8. Y. Kimhi, C. Palfrey, I. Spector, et al., "Maturation of neuroblastoma cells in the presence of dimethylsulfoxide," Proc. Nat. Acad. Sci. USA, No. 2, 462 (1976).

  9. Y. Kimhi, "Nerve cells in clonal systems," in: Excitable Cells in Tissue Culture, Plenum, New York (1981), pp. 173–246.

    Google Scholar 

  10. T. Kuramoto, K. Werrbach-Perez, J. R. Perez-Polo, and B. Haber, "Membrane properties of a human blastoma. II. Effect of differentiation," J. Neurosci. Res.,6, No. 2, 441 (1981).

    PubMed  Google Scholar 

  11. L. Legault-Demare, Y. Zeitoun, D. Lando, et al., "Expression of a specific neuronal protein 14-2-3 during in vitro differentiation of neuroblastoma cells," Exp. Cell Res.,125, No. 2, 233 (1980).

    PubMed  Google Scholar 

  12. U. Z. Littauer, C. Palfrey, Y. Kimhi, and I. Spector, "Induction of differentiation in mouse neuroblastoma cells," in: National Cancer Institute Monograph No. 48. Third Decennial Review Conference: Cell, Tissue and Organ Culture (Lake Placid, September 13–17, 1976), Plenum, New York (1978), pp. 333–337.

    Google Scholar 

  13. A. Y.-C. Liu, T. Chan, and K. Yu. Chen, "Induction of regulatory subunit of type I adenosine cyclic 3′:5′-monophosphate-dependent protein kinase in differentiated N-18 mouse neuroblastoma cells," Cancer Res.,41, No. 3, 4579 (1981).

    PubMed  Google Scholar 

  14. W. H. Moolenaar and I. Spector, "Ionic currents in cultured neuroblastoma cells under voltage clamp conditions," J. Physiol. (London),278, No. 1, 265 (1978).

    PubMed  Google Scholar 

  15. W. H. Moolenaar and I. Spector, "The calcium action potential and a prolonged calcium-dependent after-hyperpolarization in mouse neuroblastoma cells," J. Physiol. (London),292, No. 2, 297 (1979).

    PubMed  Google Scholar 

  16. W. H. Moolenaar and I. Spector, "The calcium current and the activation of a slow potassium conductance in voltage-clamped mouse neuroblastoma cells," J. Physiol. (London),292, 307 (1979).

    PubMed  Google Scholar 

  17. S. Narumi and Y. Maki, "Stimulatory effects of substance P on neurite extension and cyclic AMP levels in cultured neuroblastoma cells," J. Neurochem.,30, No. 3, 1321 (1978).

    PubMed  Google Scholar 

  18. C. Palfrey, Y. Kimhi, and U. Z. Littauer, "Induction of differentiation in mouse neuroblastoma cells by hexamethylene bisacetamide," Biochem. Biophys. Res., Commun.,76, No. 3, 937 (1977).

    Google Scholar 

  19. J. Peacock, J. Minna, and M. Nirenberg, "Use of aminopterin in selecting electrically active neuroblastoma cells," Exp. Cell Res.,73, No. 1, 367 (1972).

    Google Scholar 

  20. K. N. Prasad and A. Vernadakis, "Morphological and biochemical study in x-ray and dibutyryl cyclic AMP-induced differentiated neuroblastoma cells," Exp. Cell Res.,70, No. 1, 27 (1972).

    PubMed  Google Scholar 

  21. K. N. Prasad, J. C. Waymire, and N. Weiner, "A further study on the morphology and biochemistry of x-ray and dibutyryl cyclic AMP-induced differentiated neuroblastoma cells in culture," Exp. Cell Res.,70, No. 2, 110 (1972).

    Google Scholar 

  22. K. N. Prasad, "Differentiation of neuroblastoma cells in culture," Biol. Rev.,50, No. 2, 129 (1975).

    PubMed  Google Scholar 

  23. K. N. Prasad, E. Nobles, and K. Spuhler, "Effects of methylmercuric chloride in the presence of cyclic AMP-stimulating agents on glioma and neuroblastoma cells in culture," Environ. Res.,19, No. 2, 321 (1979).

    PubMed  Google Scholar 

  24. N. W. Seeds, A. C. Gilman, T. Amano, and M. Nirenberg, "Regulation of axon formation by clonal lines of a neural tumor," Proc. Natl. Acad. Sci. USA,66, No. 1, 160 (1970).

    PubMed  Google Scholar 

  25. D. Schubert and F. Jacob, "5-Bromodeoxyuridine-induced differentiation of a neuroblastoma," Proc. Nat. Acad. Sci. USA,67, No. 1, 247 (1970).

    PubMed  Google Scholar 

  26. I. Spector, "Electrophysiology of clonal nerve cell lines," in: Excitable Cells in Tissue Culture, Plenum, New York (1981), pp. 247–277.

    Google Scholar 

Download references

Authors

Additional information

A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 16, No. 4, pp. 519–527, July–August, 1984.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Pogorelaya, N.K., Fomina, A.F. & Veselovskii, N.S. Morphological differentiation of neuroblastoma cells induced by dimethylsulfoxide. Neurophysiology 16, 412–419 (1984). https://doi.org/10.1007/BF01053498

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01053498

Keywords

Navigation