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dc.rights.licenseopenen_US
dc.contributor.authorFRUHMANN, Gernot
hal.structure.identifierChimie et Biologie des Membranes et des Nanoobjets [CBMN]
dc.contributor.authorMARCHAL, Christelle
hal.structure.identifierChimie et Biologie des Membranes et des Nanoobjets [CBMN]
dc.contributor.authorVIGNAUD, Helene
dc.contributor.authorVERDUYCKT, Mathias
dc.contributor.authorTALAREK, Nicolas
dc.contributor.authorDE VIRGILIO, Claudio
dc.contributor.authorWINDERICKX, Joris
hal.structure.identifierChimie et Biologie des Membranes et des Nanoobjets [CBMN]
dc.contributor.authorCULLIN, Christophe
ORCID: 0000-0003-4110-4677
IDREF: 85920959
dc.date.accessioned2020-04-06T15:29:26Z
dc.date.available2020-04-06T15:29:26Z
dc.date.created2018
dc.date.issued2018
dc.identifier.issn1662-5099en_US
dc.identifier.otherhttps://www.frontiersin.org/articles/10.3389/fnmol.2018.00406/full#supplementary-materialen_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/4125
dc.description.abstractEnA beta metabolism plays a pivotal role in Alzheimer's disease. Here, we used a yeast model to monitor A beta(42) toxicity when entering the secretory pathway and demonstrate that processing in, and exit from the endoplasmic reticulum (ER) is required to unleash the full A beta(42) toxic potential. Consistent with previously reported data, our data suggests that A beta(42) interacts with mitochondria, thereby enhancing formation of reactive oxygen species and eventually leading to cell demise. We used our model to search for genes that modulate this deleterious effect, either by reducing or enhancing A beta(42) toxicity, based on screening of the yeast knockout collection. This revealed a reduced A beta(42) toxicity not only in strains hampered in ER-Golgi traffic and mitochondrial functioning but also in strains lacking genes connected to the cell cycle and the DNA replication stress response. On the other hand, increased A beta(42) toxicity was observed in strains affected in the actin cytoskeleton organization, endocytosis and the formation of multivesicular bodies, including key factors of the ESCRT machinery. Since the latter was shown to be required for the repair of membrane lesions in mammalian systems, we studied this aspect in more detail in our yeast model. Our data demonstrated that A beta(42) heavily disturbed the plasma membrane integrity in a strain lacking the ESCRT-III accessory factor Bro1, a phenotype that came along with a severe growth defect and enhanced loading of lipid droplets. Thus, it appears that also in yeast ESCRT is required for membrane repair, thereby counteracting one of the deleterious effects induced by the expression of A beta(42). Combined, our studies once more validated the use of yeast as a model to investigate fundamental mechanisms underlying the etiology of neurodegenerative disorders.
dc.language.isoENen_US
dc.subject.enAβ42
dc.subject.enamyloid beta
dc.subject.enAlzheimer’s disease
dc.subject.enESCRT
dc.subject.enmembrane repair
dc.subject.enSaccharomyces cerevisiae
dc.subject.enyeast
dc.title.enThe Impact of ESCRT on A beta(1-42) Induced Membrane Lesions in a Yeast Model for Alzheimer's Disease
dc.title.alternativeFront. Mol. Neurosci.,en_US
dc.typeArticle de revueen_US
dc.identifier.doi10.3389/fnmol.2018.00406
dc.subject.halChimie/Matériauxen_US
bordeaux.journalFrontiers in Molecular Neuroscienceen_US
bordeaux.volume11en_US
bordeaux.hal.laboratoriesInstitut de Chimie & de Biologie des Membranes & des Nano-objets (CBMN) - UMR 5248
bordeaux.institutionBordeaux INPen_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-03158274
hal.version1
hal.date.transferred2021-03-03T15:58:22Z
hal.exporttrue
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