The tardigrade Hypsibius exemplaris has the active mitochondrial alternative oxidase that could be studied at animal organismal level

PLoS One. 2021 Aug 23;16(8):e0244260. doi: 10.1371/journal.pone.0244260. eCollection 2021.

Abstract

Mitochondrial alternative oxidase (AOX) is predicted to be present in mitochondria of several invertebrate taxa including tardigrades. Independently of the reason concerning the enzyme occurrence in animal mitochondria, expression of AOX in human mitochondria is regarded as a potential therapeutic strategy. Till now, relevant data were obtained due to heterologous AOX expression in cells and animals without natively expressed AOX. Application of animals natively expressing AOX could importantly contribute to the research. Thus, we decided to investigate AOX activity in intact specimens of the tardigrade Hypsibius exemplaris. We observed that H. exemplaris specimens' tolerance to the blockage of the mitochondrial respiratory chain (MRC) cytochrome pathway was diminished in the presence of AOX inhibitor and the inhibitor-sensitive respiration enabled the tardigrade respiration under condition of the blockage. Importantly, these observations correlated with relevant changes of the mitochondrial inner membrane potential (Δψ) detected in intact animals. Moreover, detection of AOX at protein level required the MRC cytochrome pathway blockage. Overall, we demonstrated that AOX activity in tardigrades can be monitored by the animals' behavior observation as well as by measurement of intact specimens' whole-body respiration and Δψ. Furthermore, it is also possible to check the impact of the MRC cytochrome pathway blockage on AOX level as well as AOX inhibition in the absence of the blockage on animal functioning. Thus, H. exemplaris could be consider as a whole-animal model suitable to study AOX.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Behavior, Animal / physiology
  • Cell Respiration / physiology
  • Cytochromes / metabolism
  • Membrane Potential, Mitochondrial / physiology
  • Mitochondria / metabolism*
  • Mitochondria / physiology*
  • Mitochondrial Membranes / metabolism
  • Mitochondrial Membranes / physiology
  • Mitochondrial Proteins / metabolism*
  • Oxidation-Reduction
  • Oxidoreductases / metabolism*
  • Plant Proteins / metabolism*
  • Signal Transduction / physiology
  • Tardigrada / metabolism*
  • Tardigrada / physiology*

Substances

  • Cytochromes
  • Mitochondrial Proteins
  • Plant Proteins
  • Oxidoreductases
  • alternative oxidase

Grants and funding

These studies were supported by the research grant of National Science Centre, Poland, NCN 2016/21/B/NZ4/00131.