Skip to main content
Log in

Myelin basic protein does not have a mitogenic effect on adult oligodendrocytes

  • Regular Paper
  • Published:
Acta Neuropathologica Aims and scope Submit manuscript

Abstract

Increased numbers of oligodendrocytes and remyelination are frequently observed in multiple sclerosis plaques. It is presumed the increased numbers of oligodendrocytes are due to cell division, but this has not been proven. The mitogens within the lesion which might be responsible for this are unknown. Since oligodendrocyte proliferation occurs in areas in which there is myelin breakdown, we undertook the present study to determine if myelin basic protein (MBP) or its breakdown products could induce oligodendrocyte proliferation. MBP, or MBP digested by the neutral proteinase plasmin, was added in three concentrations to the media of adult bovine oligodendrocytes in culture. Oligodendrocytes were identified by staining for galactocerebroside. Bromodeoxyuridine incorporation was used as a measure of cell division. Oligodendrocytes were found to divide only rarely in regular culture media, in the presence of MBP, plasmin, or MBP digested by plasmin. The results indicate that MBP is not a significant mitogen for the mature oligodendrocyte.

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

References

  1. Benveniste EN, Merrill JE (1986) Stimulation of oligodendroglial proliferation and maturation by interleukin-2. Nature 321: 610–613

    Google Scholar 

  2. Brosnan CF, Cammer W, Norton WT, Bloom BR (1980) Proteinase inhibitors suppress the development of experimental allergic encephalomyelitis. Nature 285: 235–237

    Google Scholar 

  3. Cammer W, Brosnan CF, Basile C, Bloom BR, Norton WT (1986) Complement potentiates the degradation of myelin proteins by plasmin: implications for a mechanism of inflammatory demyelination. Brain Res 364: 91–101

    Google Scholar 

  4. Chen S-J, DeVries GH (1989) Mitogenic effect of axolemma-enriched fraction on cultured oligodendrocytes. J Neurochem 52: 325–327

    Google Scholar 

  5. DeVries GH, Salzer JL, Bunge RP (1982) Axolemma-enriched fractions isolated from PNS and CNS are mitogenic for cultured Schwann cells. Dev Brain Res 3: 295–299

    Google Scholar 

  6. Gratzner HG (1982) Monoclonal antibody to 5-bromo- and 5-iodoceoxyuridine: a new reagent for detection of DNA replication. Science 218: 474–475

    Google Scholar 

  7. Kim SU, Sato Y, Silberberg DH, Pleasure DE, Rorke LB (1983) Long-term culture of human oligodendrocytes. Isolation, growth and identification. J Neurol Sci 62: 295–301

    Google Scholar 

  8. Lee SC, Moore GRW, Golenwsky G, Raine CS (1990) Multiple sclerosis: A role for astroglia in active demyelination suggested by class II MHC expression and ultrastructural study. J Neuropathol Exp Neurol 49: 122–136

    Google Scholar 

  9. Ludwin SK (1984) Proliferation of mature oligodendrocytes following trauma to the central nervous system. Nature 308: 274–275

    Google Scholar 

  10. Moore GRW, Neumann PE, Suzuki K, Lijtmaer HN, Traugott U, Raine CS (1985) Balo's concentric sclerosis: new observations on lesion development. Ann Neurol 17: 604–611

    Google Scholar 

  11. Morell P, Quarles RH, Norton WT (1989) Formation, structure and biochemistry of myelin. In: Siegel GJ, Agranoff BW, Albers RW, Molinoff PB (eds) Basic neurochemistry. Molecular, cellular and medical aspects, 4th edn. Raven Press, New York, pp 109–136

    Google Scholar 

  12. Prineas JW (1985) The neuropathology of multiple sclerosis. In: Koetsier JC (ed) Demyelinating diseases. Handbook of clinical neurology, vol 47. Elsevier Science Publishers, Amsterdam, pp 213–257

    Google Scholar 

  13. Prineas JW, Kwon EE, Goldenberg PZ, Ilyas AA, Quarles RH, Benjamins JA, Sprinkle TJ (1989) Multiple sclerosis. Oligodendrocyte proliferation and differentiation in fresh lesions. Lab Invest 61: 489–503

    Google Scholar 

  14. Raine CS, Traugott U (1983) Chronic relapsing experimental autoimmune encephalitis. Ultrastructure of the central nervous system of animals treated with combinations of myelin components. Lab Invest 48: 275–284

    Google Scholar 

  15. Raine CS, Scheinberg L, Waltz JM (1981) Multiple sclerosis. Oligodendrocyte survival and proliferation in an active lesion. Lab Invest 45: 534–546

    Google Scholar 

  16. Ranscht B, Clapshaw PA, Price J, Noble M, Seifert W (1982) Development of oligodendrocytes and schwann cells studied with a monoclonal antibody against galactocerebroside. Proc Natl Acad Sci USA 79: 2709–2713

    Google Scholar 

  17. Ratner N, Bunge RP, Glaser L (1985) A neuronal cell surface heparan sulfate proteoglycan is required for dorsal root ganglion neuron stimulation of Schwann cell proliferation. J Cell Biol 101: 744–754

    Google Scholar 

  18. Rodriguez M, Lennon VA (1990) Immunoglobulins promote remyelination in the central nervous system. Ann Neurol 27: 12–17

    Google Scholar 

  19. Salzer JL, Bunge RP (1980) Studies of Schwann cell proliferation. I. An analysis in tissue culture of proliferation during development, Wallerian degeneration, and direct injury. J Cell Biol 84: 739–752

    Google Scholar 

  20. Saneto RP, Vellis J de (1985) Effect of mitogens in various organs and cell culture conditioned media on rat oligodendrocytes. Dev Neurosci 7: 340–350

    Google Scholar 

  21. Saneto RP, Altman A, Knobler RL, Johnson HM, Vellis J de (1986) Interleukin-2 mediates the inhibition of oligodendrocyte progenitor cell proliferation in vitro. Proc Natl Acad Sci USA 83: 9221–9225

    Google Scholar 

  22. Vick RS, DeVries GH (1993) Mitogenic potential of adult rat oligodendrocytes in culture. J Neurosci Res 33: 68–74

    Google Scholar 

  23. Wood PM, Bunge RP (1986) Evidence that axons are mitogenic for oligodendrocytes isolated from adult animals. Nature 320: 756–758

    Google Scholar 

  24. Yong VW, Kim SU, Kim MW, Shin DH (1988) Growth factors for human glial cells in culture. Glia 1: 113–123

    Google Scholar 

  25. Yoshino JE, Dinneen MP, Lewis BL, Meador-Woodruff JH, DeVries GH (1984) Differential proliferative responses of cultured Schwann cells to axolemma- and myelin-enriched fractions. I. Biochemical studies. J Cell Biol 99: 2309–2313

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Moore, G.R.W., Kim, S.U., Chang, E. et al. Myelin basic protein does not have a mitogenic effect on adult oligodendrocytes. Acta Neuropathol 89, 431–437 (1995). https://doi.org/10.1007/BF00307648

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00307648

Key words

Navigation