Alternative respiratory chain enzymes: Therapeutic potential and possible pitfalls.


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
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

854-866

Informations de copyright

Copyright © 2018 The Author(s). Published by Elsevier B.V. All rights reserved.

Auteurs

Sina Saari (S)

Faculty of Medicine and Life Sciences, BioMediTech Institute and Tampere University Hospital, FI-33014, University of Tampere, Finland. Electronic address: sina.saari@uta.fi.

Geovana S Garcia (GS)

Departamento de Tecnologia, Faculdade de Ciências Agrárias e Veterinárias, Universidade Estadual Paulista "Júlio de Mesquita Filho", 14884-900 Jaboticabal, SP, Brazil. Electronic address: geovanagarcia@grad.fcav.unesp.br.

Katharina Bremer (K)

Faculty of Medicine and Life Sciences, BioMediTech Institute and Tampere University Hospital, FI-33014, University of Tampere, Finland. Electronic address: katharina.bremer@queensu.ca.

Marina M Chioda (MM)

Departamento de Tecnologia, Faculdade de Ciências Agrárias e Veterinárias, Universidade Estadual Paulista "Júlio de Mesquita Filho", 14884-900 Jaboticabal, SP, Brazil. Electronic address: marina.chioda@posgrad.fcav.unesp.br.

Ana Andjelković (A)

Faculty of Medicine and Life Sciences, BioMediTech Institute and Tampere University Hospital, FI-33014, University of Tampere, Finland. Electronic address: ana.andjelkovic@uta.fi.

Paul V Debes (PV)

Department of Biology, FI-20014, University of Turku, Finland; Faculty of Biological and Environmental Sciences, FI-00014, University of Helsinki, Finland. Electronic address: paul.debes@dal.ca.

Mikko Nikinmaa (M)

Department of Biology, FI-20014, University of Turku, Finland. Electronic address: miknik@utu.fi.

Marten Szibor (M)

Faculty of Medicine and Life Sciences, BioMediTech Institute and Tampere University Hospital, FI-33014, University of Tampere, Finland. Electronic address: marten.szibor@uta.fi.

Eric Dufour (E)

Faculty of Medicine and Life Sciences, BioMediTech Institute and Tampere University Hospital, FI-33014, University of Tampere, Finland. Electronic address: eric.dufour@uta.fi.

Pierre Rustin (P)

INSERM UMR1141, Hôpital Robert Debré, 48, Boulevard Sérurier, 75019 Paris, France; Université Paris 7, Faculté de Médecine Denis Diderot, Paris, France. Electronic address: pierre.rustin@inserm.fr.

Marcos T Oliveira (MT)

Departamento de Tecnologia, Faculdade de Ciências Agrárias e Veterinárias, Universidade Estadual Paulista "Júlio de Mesquita Filho", 14884-900 Jaboticabal, SP, Brazil. Electronic address: marcos.t.oliveira@unesp.br.

Howard T Jacobs (HT)

Faculty of Medicine and Life Sciences, BioMediTech Institute and Tampere University Hospital, FI-33014, University of Tampere, Finland; Institute of Biotechnology, FI-00014, University of Helsinki, Finland. Electronic address: howard.t.jacobs@uta.fi.

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Classifications MeSH