Skip to main content
Journal of Neurology, Neurosurgery, and Psychiatry logoLink to Journal of Neurology, Neurosurgery, and Psychiatry
. 1991 Nov;54(11):945–948. doi: 10.1136/jnnp.54.11.945

Limiting and repairing the damage in multiple sclerosis.

A Compston
PMCID: PMC1014611  PMID: 1800662

Full text

PDF
946

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Adams C. W. The onset and progression of the lesion in multiple sclerosis. J Neurol Sci. 1975 Jun;25(2):165–182. doi: 10.1016/0022-510x(75)90138-0. [DOI] [PubMed] [Google Scholar]
  2. Aguayo A. J., Björklund A., Stenevi U., Carlstedt T. Fetal mesencephalic neurons survive and extend long axons across peripheral nervous system grafts inserted into the adult rat striatum. Neurosci Lett. 1984 Mar 9;45(1):53–58. doi: 10.1016/0304-3940(84)90328-8. [DOI] [PubMed] [Google Scholar]
  3. Blakemore W. F., Crang A. J. Extensive oligodendrocyte remyelination following injection of cultured central nervous system cells into demyelinating lesions in adult central nervous system. Dev Neurosci. 1988;10(1):1–11. doi: 10.1159/000111949. [DOI] [PubMed] [Google Scholar]
  4. Blakemore W. F., Crang A. J., Franklin R. J. Transplantation of glial cell cultures into areas of demyelination in the adult CNS. Prog Brain Res. 1990;82:225–232. doi: 10.1016/s0079-6123(08)62608-4. [DOI] [PubMed] [Google Scholar]
  5. Blakemore W. F., Crang A. J. The relationship between type-1 astrocytes, Schwann cells and oligodendrocytes following transplantation of glial cell cultures into demyelinating lesions in the adult rat spinal cord. J Neurocytol. 1989 Aug;18(4):519–528. doi: 10.1007/BF01474547. [DOI] [PubMed] [Google Scholar]
  6. Caroni P., Schwab M. E. Antibody against myelin-associated inhibitor of neurite growth neutralizes nonpermissive substrate properties of CNS white matter. Neuron. 1988 Mar;1(1):85–96. doi: 10.1016/0896-6273(88)90212-7. [DOI] [PubMed] [Google Scholar]
  7. Caroni P., Schwab M. E. Two membrane protein fractions from rat central myelin with inhibitory properties for neurite growth and fibroblast spreading. J Cell Biol. 1988 Apr;106(4):1281–1288. doi: 10.1083/jcb.106.4.1281. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Compston A., Scolding N., Wren D., Noble M. The pathogenesis of demyelinating disease: insights from cell biology. Trends Neurosci. 1991 May;14(5):175–182. doi: 10.1016/0166-2236(91)90099-g. [DOI] [PubMed] [Google Scholar]
  9. Dunnett S. B. Transplantation of embryonic dopamine neurons: what we know from rats. J Neurol. 1991 Apr;238(2):65–74. doi: 10.1007/BF00315683. [DOI] [PubMed] [Google Scholar]
  10. Fawcett J. W., Housden E., Smith-Thomas L., Meyer R. L. The growth of axons in three-dimensional astrocyte cultures. Dev Biol. 1989 Oct;135(2):449–458. doi: 10.1016/0012-1606(89)90193-0. [DOI] [PubMed] [Google Scholar]
  11. Fawcett J. W., Rokos J., Bakst I. Oligodendrocytes repel axons and cause axonal growth cone collapse. J Cell Sci. 1989 Jan;92(Pt 1):93–100. doi: 10.1242/jcs.92.1.93. [DOI] [PubMed] [Google Scholar]
  12. Ffrench-Constant C., Raff M. C. Proliferating bipotential glial progenitor cells in adult rat optic nerve. Nature. 1986 Feb 6;319(6053):499–502. doi: 10.1038/319499a0. [DOI] [PubMed] [Google Scholar]
  13. Franklin R. J., Crang A. J., Blakemore W. F. Transplanted type-1 astrocytes facilitate repair of demyelinating lesions by host oligodendrocytes in adult rat spinal cord. J Neurocytol. 1991 May;20(5):420–430. doi: 10.1007/BF01355538. [DOI] [PubMed] [Google Scholar]
  14. Kesselring J., Miller D. H., MacManus D. G., Johnson G., Milligan N. M., Scolding N., Compston D. A., McDonald W. I. Quantitative magnetic resonance imaging in multiple sclerosis: the effect of high dose intravenous methylprednisolone. J Neurol Neurosurg Psychiatry. 1989 Jan;52(1):14–17. doi: 10.1136/jnnp.52.1.14. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Lindvall O., Brundin P., Widner H., Rehncrona S., Gustavii B., Frackowiak R., Leenders K. L., Sawle G., Rothwell J. C., Marsden C. D. Grafts of fetal dopamine neurons survive and improve motor function in Parkinson's disease. Science. 1990 Feb 2;247(4942):574–577. doi: 10.1126/science.2105529. [DOI] [PubMed] [Google Scholar]
  16. McDonald W. I., Barnes D. Lessons from magnetic resonance imaging in multiple sclerosis. Trends Neurosci. 1989 Oct;12(10):376–379. doi: 10.1016/0166-2236(89)90075-1. [DOI] [PubMed] [Google Scholar]
  17. Miller R. H., Ffrench-Constant C., Raff M. C. The macroglial cells of the rat optic nerve. Annu Rev Neurosci. 1989;12:517–534. doi: 10.1146/annurev.ne.12.030189.002505. [DOI] [PubMed] [Google Scholar]
  18. Miller Robert H., Fulton Barbara P., Raff Martin C. A Novel Type of Glial Cell Associated with Nodes of Ranvier in Rat Optic Nerve. Eur J Neurosci. 1989 Mar;1(2):172–180. doi: 10.1111/j.1460-9568.1989.tb00785.x. [DOI] [PubMed] [Google Scholar]
  19. Noble M., Murray K., Stroobant P., Waterfield M. D., Riddle P. Platelet-derived growth factor promotes division and motility and inhibits premature differentiation of the oligodendrocyte/type-2 astrocyte progenitor cell. Nature. 1988 Jun 9;333(6173):560–562. doi: 10.1038/333560a0. [DOI] [PubMed] [Google Scholar]
  20. Prineas J. W., Connell F. Remyelination in multiple sclerosis. Ann Neurol. 1979 Jan;5(1):22–31. doi: 10.1002/ana.410050105. [DOI] [PubMed] [Google Scholar]
  21. Raff M. C., Miller R. H., Noble M. A glial progenitor cell that develops in vitro into an astrocyte or an oligodendrocyte depending on culture medium. Nature. 1983 Jun 2;303(5916):390–396. doi: 10.1038/303390a0. [DOI] [PubMed] [Google Scholar]
  22. Ransom B. R., Butt A. M., Black J. A. Ultrastructural identification of HRP-injected oligodendrocytes in the intact rat optic nerve. Glia. 1991;4(1):37–45. doi: 10.1002/glia.440040105. [DOI] [PubMed] [Google Scholar]
  23. Schnell L., Schwab M. E. Axonal regeneration in the rat spinal cord produced by an antibody against myelin-associated neurite growth inhibitors. Nature. 1990 Jan 18;343(6255):269–272. doi: 10.1038/343269a0. [DOI] [PubMed] [Google Scholar]
  24. Scolding N. J., Compston D. A. Oligodendrocyte-macrophage interactions in vitro triggered by specific antibodies. Immunology. 1991 Jan;72(1):127–132. [PMC free article] [PubMed] [Google Scholar]
  25. Scolding N. J., Houston W. A., Morgan B. P., Campbell A. K., Compston D. A. Reversible injury of cultured rat oligodendrocytes by complement. Immunology. 1989 Aug;67(4):441–446. [PMC free article] [PubMed] [Google Scholar]
  26. Scolding N. J., Jones J., Compston D. A., Morgan B. P. Oligodendrocyte susceptibility to injury by T-cell perforin. Immunology. 1990 May;70(1):6–10. [PMC free article] [PubMed] [Google Scholar]
  27. Scolding N. J., Morgan B. P., Houston A., Campbell A. K., Linington C., Compston D. A. Normal rat serum cytotoxicity against syngeneic oligodendrocytes. Complement activation and attack in the absence of anti-myelin antibodies. J Neurol Sci. 1989 Feb;89(2-3):289–300. doi: 10.1016/0022-510x(89)90030-0. [DOI] [PubMed] [Google Scholar]
  28. Scolding N. J., Morgan B. P., Houston W. A., Linington C., Campbell A. K., Compston D. A. Vesicular removal by oligodendrocytes of membrane attack complexes formed by activated complement. Nature. 1989 Jun 22;339(6226):620–622. doi: 10.1038/339620a0. [DOI] [PubMed] [Google Scholar]
  29. Smith K. J., Hall S. M., Schauf C. L. Vesicular demyelination induced by raised intracellular calcium. J Neurol Sci. 1985 Nov;71(1):19–37. doi: 10.1016/0022-510x(85)90034-6. [DOI] [PubMed] [Google Scholar]
  30. Springer T. A. Adhesion receptors of the immune system. Nature. 1990 Aug 2;346(6283):425–434. doi: 10.1038/346425a0. [DOI] [PubMed] [Google Scholar]
  31. Thompson A. J., Kermode A. G., Wicks D., MacManus D. G., Kendall B. E., Kingsley D. P., McDonald W. I. Major differences in the dynamics of primary and secondary progressive multiple sclerosis. Ann Neurol. 1991 Jan;29(1):53–62. doi: 10.1002/ana.410290111. [DOI] [PubMed] [Google Scholar]
  32. Weinshenker B. G., Bass B., Rice G. P., Noseworthy J., Carriere W., Baskerville J., Ebers G. C. The natural history of multiple sclerosis: a geographically based study. 2. Predictive value of the early clinical course. Brain. 1989 Dec;112(Pt 6):1419–1428. doi: 10.1093/brain/112.6.1419. [DOI] [PubMed] [Google Scholar]
  33. Winter G., Milstein C. Man-made antibodies. Nature. 1991 Jan 24;349(6307):293–299. doi: 10.1038/349293a0. [DOI] [PubMed] [Google Scholar]
  34. Wolswijk G., Noble M. Identification of an adult-specific glial progenitor cell. Development. 1989 Feb;105(2):387–400. doi: 10.1242/dev.105.2.387. [DOI] [PubMed] [Google Scholar]
  35. Wren D. R., Noble M. Oligodendrocytes and oligodendrocyte/type-2 astrocyte progenitor cells of adult rats are specifically susceptible to the lytic effects of complement in absence of antibody. Proc Natl Acad Sci U S A. 1989 Nov;86(22):9025–9029. doi: 10.1073/pnas.86.22.9025. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Neurology, Neurosurgery, and Psychiatry are provided here courtesy of BMJ Publishing Group

RESOURCES