Early redox activities modulate Xenopus tail regeneration.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 30327466.
- Also identified by DOI 10.1038/s41467-018-06614-2 and PMC identifier 6191437.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Redox state sustained by reactive oxygen species (ROS) is crucial for regeneration; however, the interplay between oxygen (O<sub>2</sub>), ROS and hypoxia-inducible factors (HIF) remains elusive. Here we observe, using an optic-based probe (optrode), an elevated and steady O<sub>2</sub> influx immediately upon amputation. The spatiotemporal O<sub>2</sub> influx profile correlates with the regeneration of Xenopus laevis tadpole tails. Inhibition of ROS production but not ROS scavenging decreases O<sub>2</sub> influx. Inhibition of HIF-1α impairs regeneration and stabilization of HIF-1α induces regeneration in the refractory period. In the regeneration bud, hypoxia correlates with O<sub>2</sub> influx, ROS production, and HIF-1α stabilization that modulate regeneration. Further analyses reveal that heat shock protein 90 is a putative downstream target of HIF-1α while electric current reversal is a de facto downstream target of HIF-1α. Collectively, the results show a mechanism for regeneration via the orchestration of O<sub>2</sub> influx, ROS production, and HIF-1α stabilization.
Medical subject headings
- Oxygen
- Regeneration
- Tail
- Xenopus laevis