Low abundance of NDUFV2 and NDUFS4 subunits of the hydrophilic complex I domain and VDAC1 predicts mammalian longevity

dc.contributor.author
Mota Martorell, Natàlia
dc.contributor.author
Jové Font, Mariona
dc.contributor.author
Pradas Barriga, Irene
dc.contributor.author
Sanchez, Isabel
dc.contributor.author
Gómez, José
dc.contributor.author
Naudí i Farré, Alba
dc.contributor.author
Barja, Gustavo
dc.contributor.author
Pamplona Gras, Reinald
dc.date.accessioned
2024-12-05T21:56:17Z
dc.date.available
2024-12-05T21:56:17Z
dc.date.issued
2021-03-09T07:24:13Z
dc.date.issued
2021-03-09T07:24:13Z
dc.date.issued
2020-07-01
dc.date.issued
2021-03-09T07:24:13Z
dc.identifier
https://doi.org/10.1016/j.redox.2020.101539
dc.identifier
2213-2317
dc.identifier
http://hdl.handle.net/10459.1/70698
dc.identifier.uri
http://hdl.handle.net/10459.1/70698
dc.description.abstract
Mitochondrial reactive oxygen species (ROS) production, specifically at complex I (Cx I), has been widely suggested to be one of the determinants of species longevity. The present study follows a comparative approach to analyse complex I in heart tissue from 8 mammalian species with a longevity ranging from 3.5 to 46 years. Gene expression and protein content of selected Cx I subunits were analysed using droplet digital PCR (ddPCR) and western blot, respectively. Our results demonstrate: 1) the existence of species-specific differences in gene expression and protein content of Cx I in relation to longevity; 2) the achievement of a longevity phenotype is associated with low protein abundance of subunits NDUFV2 and NDUFS4 from the matrix hydrophilic domain of Cx I; and 3) long-lived mammals show also lower levels of VDAC (voltage-dependent anion channel) amount. These differences could be associated with the lower mitochondrial ROS production and slower aging rate of long-lived animals and, unexpectedly, with a low content of the mitochondrial permeability transition pore in these species.
dc.description.abstract
This work was supported by the Spanish Ministry of Economy and Competitiveness, Institute of Health Carlos III (grant number PI14/00328), the Spanish Ministry of Science, Innovation and Universities (RTI2018-099200-B-I00), and the Generalitat of Catalonia, Agency for Management of University and Research Grants (2017SGR696) and Department of Health (SLT002/16/00250) to R.P, and PR [19] BIO MET 0155 to GB.This study has been co-financed by FEDER funds from the European Union (“A way to build Europe”). IRBLleida is a CERCA Programme/Generalitat of Catalonia.
dc.format
application/pdf
dc.language
eng
dc.publisher
Elsevier
dc.relation
info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/RTI2018-099200-B-I00/ES/NEUROLIPIDOMICA DEL ENVEJECIMIENTO CEREBRAL HUMANO/
dc.relation
Reproducció del document publicat a: https://doi.org/10.1016/j.redox.2020.101539
dc.relation
Redox Biology, 2020, vol. 34, núm. 101539, p. 1-10
dc.rights
cc-by-nc-nd (c) Mota Martorell et al., 2020
dc.rights
info:eu-repo/semantics/openAccess
dc.rights
http://creativecommons.org/licenses/by-nc-nd/3.0/es
dc.subject
Complex I
dc.subject
Droplet digital PCR
dc.subject
Longevity
dc.subject
Mammals
dc.subject
Mitochondria
dc.subject
NDUFV2 subunit
dc.subject
NDUFS4 subunit
dc.subject
VDAC
dc.subject
Western blot
dc.title
Low abundance of NDUFV2 and NDUFS4 subunits of the hydrophilic complex I domain and VDAC1 predicts mammalian longevity
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion


Ficheros en el ítem

FicherosTamañoFormatoVer

No hay ficheros asociados a este ítem.

Este ítem aparece en la(s) siguiente(s) colección(ones)