Nutrient availability contributes to a graded refractory period for regeneration in Xenopus tropicalis

Dev Biol. 2021 May:473:59-70. doi: 10.1016/j.ydbio.2021.01.005. Epub 2021 Jan 20.

Abstract

Xenopus tadpoles are a unique model for regeneration in that they exhibit two distinct phases of age-specific regenerative competence. In Xenopus laevis, young tadpoles fully regenerate following major injuries such as tail transection, then transiently lose regenerative competence during the "refractory period" from stages 45-47. Regenerative competence is then regained in older tadpoles before being permanently lost during metamorphosis. Here we show that a similar refractory period exists in X. tropicalis. Notably, tadpoles lose regenerative competence gradually in X. tropicalis, with full regenerative competence lost at stage 47. We find that the refractory period coincides closely with depletion of maternal yolk stores and the onset of independent feeding, and so we hypothesized that it might be caused in part by nutrient stress. In support of this hypothesis, we find that cell proliferation declines throughout the tail as the refractory period approaches. When we block nutrient mobilization by inhibiting mTOR signaling, we find that tadpole growth and regeneration are reduced, while yolk stores persist. Finally, we are able to restore regenerative competence and cell proliferation during the refractory period by abundantly feeding tadpoles. Our study argues that nutrient stress contributes to lack of regenerative competence and introduces the X. tropicalis refractory period as a valuable new model for interrogating how metabolic constraints inform regeneration.

Keywords: Nutrient availability; Nutrient stress; Refractory period; Tail regeneration; Vitellogenin; Xenopus; Xenopus tropicalis; mTOR.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Cell Proliferation
  • Egg Yolk
  • Larva / metabolism
  • Metamorphosis, Biological / physiology
  • Nutrients
  • Regeneration / physiology*
  • Signal Transduction
  • Tail / physiology*
  • Xenopus / embryology*
  • Xenopus / metabolism
  • Xenopus Proteins / metabolism

Substances

  • Xenopus Proteins