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. Retinoid X receptor α downregulation is required for tail and caudal spinal cord regeneration in the adult newt

Retinoid X receptor α downregulation is required for tail and caudal spinal cord regeneration in the adult newt

Neural Regeneration Research, 2018 · DOI: 10.4103/1673-5374.233447 · Published: June 1, 2018

Regenerative MedicineNeurologyGenetics

Simple Explanation

This research investigates the role of retinoid X receptor α (RXRα) in tail and spinal cord regeneration in newts. The study found that RXRα protein levels decrease during regeneration, while a related protein, retinoic acid receptor β (RARβ), increases. The researchers used drugs to manipulate RXRα and RARβ activity. They discovered that preventing the decrease of RXRα with an RXR agonist, SR11237, inhibits tail and spinal cord regeneration. Similarly, blocking RARβ with an antagonist, LE135, also inhibits regeneration and interestingly, also prevents the normal downregulation of RXRα. The findings suggest a regulatory relationship between RXRα and RARβ. The proper balance of these proteins, with RXRα decreasing and RARβ increasing, is necessary for successful tail and spinal cord regeneration in newts.

Study Duration
21 days
Participants
Adult eastern red-spotted newts, Notophthalmus viridescens
Evidence Level
Not specified

Key Findings

  • 1
    RXRα protein levels decrease during tail and spinal cord regeneration in adult newts, while RXRα mRNA levels increase.
  • 2
    Pharmacological activation of RXR with SR11237 inhibits tail and spinal cord regeneration and prevents the downregulation of RXRα and upregulation of RARβ.
  • 3
    Inhibition of RARβ with LE135 also inhibits regeneration and prevents the downregulation of RXRα, suggesting a regulatory feedback loop between the two receptors.

Research Summary

This study investigates the role of RXRα in tail and spinal cord regeneration in adult newts, focusing on its interaction with RARβ. The research demonstrates that RXRα protein levels are downregulated during regeneration, a process necessary for proper tissue regrowth. Manipulating RXRα and RARβ levels pharmacologically disrupts regeneration. The findings suggest an indirect regulatory feedback loop between RXRα and RARβ, highlighting the complexity of retinoid signaling in spinal cord regeneration.

Practical Implications

Potential Therapeutic Targets

The study identifies RXRα and RARβ as potential therapeutic targets for promoting spinal cord regeneration. Further research could explore how to modulate these receptors to enhance regenerative capacity in humans.

Understanding Regulatory Networks

The discovery of a regulatory feedback loop between RXRα and RARβ provides insights into the complex molecular networks that govern regeneration. This knowledge can be used to develop more effective strategies for regenerative medicine.

Comparative Biology

Comparing the role of RXRα and RARβ in regeneration-competent species like newts to their role in regeneration-incompetent species like mammals may reveal key differences that explain why some species can regenerate while others cannot.

Study Limitations

  • 1
    The study focuses on a specific time window (21 days post-amputation) and may not capture the full spectrum of RXRα and RARβ dynamics.
  • 2
    The mechanisms underlying the post-transcriptional regulation of RXRα are not fully elucidated.
  • 3
    The precise cellular and molecular interactions between RXRα and RARβ remain to be fully determined.

Your Feedback

Was this summary helpful?

Back to Regenerative Medicine