Spinal Cord Research Help
AboutCategoriesLatest ResearchContact
Subscribe
Spinal Cord Research Help

Making Spinal Cord Injury (SCI) Research Accessible to Everyone. Simplified summaries of the latest research, designed for patients, caregivers and anybody who's interested.

Quick Links

  • Home
  • About
  • Categories
  • Latest Research
  • Disclaimer

Contact

  • Contact Us
© 2025 Spinal Cord Research Help

All rights reserved.

  1. Home
  2. Research
  3. Regenerative Medicine
  4. Regeneration of neural crest derivatives in the Xenopus tadpole tail

Regeneration of neural crest derivatives in the Xenopus tadpole tail

BMC Developmental Biology, 2007 · DOI: 10.1186/1471-213X-7-56 · Published: May 24, 2007

Regenerative MedicineGenetics

Simple Explanation

After a Xenopus tadpole loses its tail, it can regrow a new one. This study looks at how certain cell types called neural crest derivatives, specifically pigment cells and nerve cells, regenerate in the new tail. The study found that pigment cells (melanophores) do regenerate in the new tail, and they come from existing precursor cells near the amputation site. However, the nerve clusters (spinal ganglia) do not regenerate well. Even though the spinal ganglia don't fully regenerate, the new tail does develop some sensory systems, allowing it to function. The regeneration process doesn't recreate the exact conditions of the original embryonic development.

Study Duration
Not specified
Participants
Xenopus laevis tadpoles
Evidence Level
Not specified

Key Findings

  • 1
    Cells do not emigrate from the spinal cord during tail regeneration, indicating that a new neural crest is not induced as in embryonic development.
  • 2
    Spinal ganglia are not regenerated in the tail, but sensory neurons are regenerated within the spinal cord, and there is sensory innervation of the skin.
  • 3
    Melanophores in the regenerated tail originate from pre-existing melanophore precursors near the amputation site, not from the spinal cord or other non-neural crest-derived cells.

Research Summary

This study investigates the regeneration of neural crest derivatives, specifically melanophores and spinal ganglia, in the Xenopus tadpole tail after amputation. The findings indicate that melanophores regenerate from unpigmented precursors, while spinal ganglia are not re-formed, although sensory neurons regenerate within the spinal cord. The study concludes that the regenerated tail, while functional, is not an exact replica of the original and does not involve the induction of a new neural crest.

Practical Implications

Understanding Regeneration Mechanisms

Provides insights into the specific cellular origins and processes involved in tissue regeneration in vertebrates.

Differences Between Embryonic Development and Regeneration

Highlights the differences between embryonic development and regeneration, showing that regeneration does not simply recapitulate embryonic processes.

Potential Therapeutic Applications

May contribute to future research on regenerative medicine by identifying factors and mechanisms that promote tissue regeneration.

Study Limitations

  • 1
    The study focuses solely on the Xenopus tadpole tail, and the results may not be generalizable to other species or tissues.
  • 2
    The exact molecular signals and pathways involved in the activation of melanophore precursors are not fully elucidated.
  • 3
    The study does not address the long-term functional consequences of the incomplete regeneration of spinal ganglia.

Your Feedback

Was this summary helpful?

Back to Regenerative Medicine