Alternative respiratory chain enzymes: Therapeutic potential and possible pitfalls.
AOX
Mitochondria
Mitochondrial disease
Reactive oxygen species
Thermogenesis
Journal
Biochimica et biophysica acta. Molecular basis of disease
ISSN: 1879-260X
Titre abrégé: Biochim Biophys Acta Mol Basis Dis
Pays: Netherlands
ID NLM: 101731730
Informations de publication
Date de publication:
01 04 2019
01 04 2019
Historique:
received:
20
05
2018
revised:
03
10
2018
accepted:
05
10
2018
pubmed:
21
10
2018
medline:
30
11
2019
entrez:
21
10
2018
Statut:
ppublish
Résumé
The alternative respiratory chain (aRC), comprising the alternative NADH dehydrogenases (NDX) and quinone oxidases (AOX), is found in microbes, fungi and plants, where it buffers stresses arising from restrictions on electron flow in the oxidative phosphorylation system. The aRC enzymes are also found in species belonging to most metazoan phyla, including some chordates and arthropods species, although not in vertebrates or in Drosophila. We postulated that the aRC enzymes might be deployed to alleviate pathological stresses arising from mitochondrial dysfunction in a wide variety of disease states. However, before such therapies can be contemplated, it is essential to understand the effects of aRC enzymes on cell metabolism and organismal physiology. Here we report and discuss new findings that shed light on the functions of the aRC enzymes in animals, and the unexpected benefits and detriments that they confer on model organisms. In Ciona intestinalis, the aRC is induced by hypoxia and by sulfide, but is unresponsive to other environmental stressors. When expressed in Drosophila, AOX results in impaired survival under restricted nutrition, in addition to the previously reported male reproductive anomalies. In contrast, it confers cold resistance to developing and adult flies, and counteracts cell signaling defects that underlie developmental dysmorphologies. The aRC enzymes may also influence lifespan and stress resistance more generally, by eliciting or interfering with hormetic mechanisms. In sum, their judicious use may lead to major benefits in medicine, but this will require a thorough characterization of their properties and physiological effects.
Identifiants
pubmed: 30342157
pii: S0925-4439(18)30389-2
doi: 10.1016/j.bbadis.2018.10.012
pii:
doi:
Substances chimiques
Drosophila Proteins
0
NADH duroquinone reductase
EC 1.6.99.-
Quinone Reductases
EC 1.6.99.-
NADH Dehydrogenase
EC 1.6.99.3
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
854-866Informations de copyright
Copyright © 2018 The Author(s). Published by Elsevier B.V. All rights reserved.