Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Letter
  • Published:

The oligodendrocyte-type-2 astrocyte cell lineage is specialized for myelination

Abstract

Astrocytes are one of the most numerous cell types in the vertebrate central nervous system (CNS) and yet their functions are largely unknown. In the rat optic nerve there are two distinct types of astrocyte1: type-1 astrocytes develop from one type of precursor cell2, and type-2 astrocytes develop from bipotential, oligodendrocyte-type-2 astrocyte (O-2A) progenitor cells3, that initially give rise to oligodendrocytes (which make myelin in the CNS), and then to type-2 astrocytes4. Type-1 astrocytes form the glial limiting membrane at the periphery of the optic nerve5 and are probably responsible for glial scar formation following nerve transection6. The functions of type-2 astrocytes, which, like oligodendrocytes, are found mainly in tracts of myelinated axons throughout the CNS6, are unknown. In this report we provide evidence that processes from type-2 astrocytes contribute to the structure of nodes of Ranvier, suggesting that the O-2 A cell lineage is specialized for constructing myelin sheaths and nodes in the mammalian CNS.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Similar content being viewed by others

References

  1. Raff, M. C., Abney, E. R., Cohen, J., Lindsay, R. & Noble, M. J. Neurosci. 3, 1289–1300 (1983).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  2. Raff, M. C., Abney, E. R. & Miller, R. H. Devl Biol. 106, 53–60 (1984).

    Article  CAS  Google Scholar 

  3. Raff, M. C., Miller, R. H. & Noble, M. Nature 303, 390–396 (1983).

    Article  ADS  CAS  PubMed  Google Scholar 

  4. Miller, R. H., David, S., Patel, R., Abney, E. R. & Raff, M. C. Devl Biol. 111, 35–41 (1985).

    Article  CAS  Google Scholar 

  5. Miller, R. H. & Raff, M. C. J. Neurosci. 4, 585–592 (1984).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Miller, R. H. et al. J. Neurosci. 6, 22–29 (1986).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  7. Waxman, S. G. & Ritchie, J. M. Science 228, 1502–1507 (1985).

    Article  ADS  CAS  PubMed  Google Scholar 

  8. Waxman, S. G. Trends Neurosci. 9, 250–253 (1986).

    Article  Google Scholar 

  9. Kruse, J., Keilhauer, G., Faissner, A., Timpl, R. & Schachner, M. Nature 316, 146–148 (1985).

    Article  ADS  CAS  PubMed  Google Scholar 

  10. ffrench-Constant, C., Miller, R. H., Kruse, J., Schachner, M. & Raff, M. C. J. Cell Biol. 102, 844–852 (1986).

    Article  CAS  PubMed  Google Scholar 

  11. Rougon, G., Hirsch, M. R., Hirn, M., Guenet, J. L. Goridis, C. Neuroscience 10, 511–520 (1983).

    Article  CAS  PubMed  Google Scholar 

  12. Bignami, A., Eng, L. F., Dahl, D. & Uyeda, C. T. Brain Res. 43, 429–435 (1972).

    Article  CAS  PubMed  Google Scholar 

  13. Raff, M. C. et al. Brain Res. 174, 283–308 (1979).

    Article  CAS  PubMed  Google Scholar 

  14. Eisenbarth, G. S., Walsh, F. S. & Nirenberg, M. Proc. natn. Acad. Sci. U.S.A. 76, 4913–4917 (1979).

    Article  ADS  CAS  Google Scholar 

  15. Raff, M. C., Williams, B. P. & Miller, R. H. EMBO J. 3, 1857–1864 (1984).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Raff, M. C., Abney, E. R. & Fok-Seang, J. Cell 42, 61–69 (1985).

    Article  CAS  PubMed  Google Scholar 

  17. Noble, M. & Murray, K. EMBO J. 3, 2243–2247 (1984).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  18. Temple, S. & Raff, M. C. Cell 44, 773–779 (1986).

    Article  CAS  PubMed  Google Scholar 

  19. Ranscht, B., Clapshaw, P. A., Price, J., Noble, M. & Seifert, W. Proc. natn. Acad. Sci. U.S.A. 79, 2709–2713 (1982).

    Article  ADS  CAS  Google Scholar 

  20. Tartakoff, A. M. Cell 32, 1026–1028 (1983).

    Article  CAS  PubMed  Google Scholar 

  21. Hildebrand, C. & Waxman, S. G. J. comp. Neurol. 224, 25–37 (1984).

    Article  CAS  PubMed  Google Scholar 

  22. Sims, T.J., Waxman, S. G., Black, J. A. & Gilmore, S. A. Brain Res. 337, 321–331 (1985).

    Article  CAS  PubMed  Google Scholar 

  23. Vaughn, J. E. & Peters, A. Am. J. Anat. 121, 131–152 (1967).

    Article  CAS  PubMed  Google Scholar 

  24. Moore, M. A. S., Williams, N. & Metcalf, D. J. cell Physiol. 79, 283–292 (1972).

    Article  CAS  PubMed  Google Scholar 

  25. Pruss, R. M. Nature 280, 688–690 (1979).

    Article  ADS  CAS  PubMed  Google Scholar 

  26. ffrench-Constant, C. & Raff, M. C. Nature 319, 499–502 (1986).

    Article  ADS  CAS  PubMed  Google Scholar 

  27. Bottenstein, J. E. & Sato, G. H. Proc. natn. Acad. Sci. U.S.A. 76, 514–517 (1979).

    Article  ADS  CAS  Google Scholar 

  28. Sarmiento, M., Glasebrook, A. L. & Pitch, F. W. J. Immun. 125, 2665–72 (1980).

    CAS  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

ffrench-Constant, C., Raff, M. The oligodendrocyte-type-2 astrocyte cell lineage is specialized for myelination. Nature 323, 335–338 (1986). https://doi.org/10.1038/323335a0

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1038/323335a0

This article is cited by

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing