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