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Bcl-2 promotes regeneration of severed axons in mammalian CNS

Author

Listed:
  • Dong Feng Chen

    (Howard Hughes Medical Institute, Center for Learning and Memory, Center for Cancer Research
    Massachusetts Institute of Technology
    Massachusetts Institute of Technology)

  • Gerald E. Schneider

    (Massachusetts Institute of Technology)

  • Jean-Claude Martinou
  • Susumu Tonegawa

    (Howard Hughes Medical Institute, Center for Learning and Memory, Center for Cancer Research
    Massachusetts Institute of Technology
    Massachusetts Institute of Technology)

Abstract

Most neurons of the mammalian central nervous system (CNS) lose the ability to regenerate severed axons in vivo after a certain point in development1. At least part of this loss in regenerative potential is intrinsic to neurons2–4. Although embryonic retinal ganglion cells (RGCs) can grow axons into tectum of any age, most RGCs from older animals fail to extend axons into CNS tissue derived from donors of any age, including the embryonic tectum2. Here we report that the proto-oncogene bcl-2 plays a key role in this developmental change by promoting the growth and regeneration of retinal axons. This effect does not seem to be an indirect consequence of its well-known anti-apoptotic activity. Another anti-apoptotic drug, ZVAD, supported neuronal survival but did not promote axon regeneration in culture. This finding could lead to new strategies for the treatment of injuries to the CNS.

Suggested Citation

  • Dong Feng Chen & Gerald E. Schneider & Jean-Claude Martinou & Susumu Tonegawa, 1997. "Bcl-2 promotes regeneration of severed axons in mammalian CNS," Nature, Nature, vol. 385(6615), pages 434-439, January.
    • Handle: RePEc:nat:nature:v:385:y:1997:i:6615:d:10.1038_385434a0
    DOI: 10.1038/385434a0
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