Bioenergetic and Autophagic Characterization of Skin Fibroblasts from C9orf72 Patients.

dc.contributor.authorAlvarez Mora, Maria Isabel
dc.contributor.authorGarrabou Tornos, Glòria
dc.contributor.authorBarcos Rodríguez, Tamara
dc.contributor.authorGarcia-Garcia, Francisco
dc.contributor.authorGrillo Risco, Ruben
dc.contributor.authorPeruga, Emma
dc.contributor.authorGort i Mas, Laura
dc.contributor.authorBorrego Écija, Sergi
dc.contributor.authorSanchez-Valle, Raquel
dc.contributor.authorCantó Santos, Judith
dc.contributor.authorNavarro Navarro, Paula
dc.contributor.authorRodriguez Revenga, Laia
dc.date.accessioned2022-11-18T17:57:51Z
dc.date.available2022-11-18T17:57:51Z
dc.date.issued2022-06-08
dc.date.updated2022-11-18T17:57:51Z
dc.description.abstractThe objective of this study is to describe the alterations occurring during the neurodegenerative process in skin fibroblast cultures from C9orf72 patients. We characterized the oxidative stress, autophagy flux, small ubiquitin-related protein SUMO2/3 levels as well as the mitochondrial function in skin fibroblast cultures from C9orf72 patients. All metabolic and bioenergetic findings were further correlated with gene expression data obtained from RNA sequencing analysis. Fibroblasts from C9orf72 patients showed a 30% reduced expression of C9orf72, ~3-fold increased levels of oxidative stress and impaired mitochondrial function obtained by measuring the enzymatic activities of mitochondrial respiratory chain complexes, specifically of complex III activity. Furthermore, the results also reveal that C9orf72 patients showed an accumulation of p62 protein levels, suggesting the alteration of the autophagy process, and significantly higher protein levels of SUMO2/3 (p = 0.03). Our results provide new data reinforcing that C9orf72 cells suffer from elevated oxidative damage to biomolecules and organelles and from increased protein loads, leading to insufficient autophagy and an increase in SUMOylation processes.
dc.format.extent14 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec724893
dc.identifier.idimarina9315982
dc.identifier.issn2076-3921
dc.identifier.pmid35740026
dc.identifier.urihttps://hdl.handle.net/2445/191013
dc.language.isoeng
dc.publisherMDPI
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.3390/antiox11061129
dc.relation.ispartofAntioxidants, 2022, vol. 11, num. 6, p. 1129
dc.relation.urihttps://doi.org/10.3390/antiox11061129
dc.rightscc-by (c) Alvarez-Mora, Maria Isabel et al., 2022
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceArticles publicats en revistes (Medicina)
dc.subject.classificationPell
dc.subject.classificationFibroblasts
dc.subject.classificationExpressió gènica
dc.subject.classificationBioenergètica
dc.subject.classificationAutofàgia
dc.subject.classificationCèl·lules
dc.subject.classificationEstrès oxidatiu
dc.subject.otherSkin
dc.subject.otherFibroblasts
dc.subject.otherGene expression
dc.subject.otherBioenergetics
dc.subject.otherAutophagy
dc.subject.otherCells
dc.subject.otherOxidative stress
dc.titleBioenergetic and Autophagic Characterization of Skin Fibroblasts from C9orf72 Patients.
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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