Anomalies occurring in lipid profiles and protein distribution in frontal cortex lipid rafts in dementia with Lewy bodies disclose neurochemical traits partially shared by Alzheimer's and Parkinson's diseases

dc.contributor.authorMarín, Raquel
dc.contributor.authorFabelo, Noemí
dc.contributor.authorMartín, Virginia
dc.contributor.authorGarcia Esparcia, Paula
dc.contributor.authorFerrer, Isidro (Ferrer Abizanda)
dc.contributor.authorQuinto-Alemany, David
dc.contributor.authorDíaz, Mario
dc.date.accessioned2019-07-16T11:16:07Z
dc.date.available2019-07-16T11:16:07Z
dc.date.issued2017-01
dc.date.updated2019-07-16T11:16:08Z
dc.description.abstractLipid rafts are highly dynamic membrane microdomains intimately associated with cell signaling. Compelling evidence has demonstrated that alterations in lipid rafts are associated with neurodegenerative diseases such Alzheimer's disease, but at present, whether alterations in lipid raft microdomains occurs in other types of dementia such Dementia with Lewy Bodies (DLB) remains unknown. Our analyses reveal that lipid rafts from DLB exhibit aberrant lipid profiles including low levels of n3 long chain polyunsaturated fatty acids (mainly docosahexaenoic acid), plasmalogens and cholesterol, and reduced unsaturation and peroxidability indexes. As a consequence, lipid raft resident proteins holding principal factors of the βamyloidogenic pathway, including β-amyloid precursor protein, presenilin 1, βsecretase and PrP, are redistributed between lipid rafts and non-raft domains in DLB frontal cortex. Meta-analysis discloses certain similarities in the altered composition of lipid rafts between DLB and Parkinson's disease which are in line with the spectrum of Lewy Body Diseases. In addition, redistribution of proteins linked to the β-amyloidogenic pathway in DLB can facilitate generation of β-amyloid, thus providing mechanistic clues to the intriguing convergence of Alzheimer's disease pathology, particularly β-amyloid deposition, in DLB.
dc.format.extent8 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec689774
dc.identifier.issn0197-4580
dc.identifier.pmid27768960
dc.identifier.urihttps://hdl.handle.net/2445/137303
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1016/j.neurobiolaging.2016.08.027
dc.relation.ispartofNeurobiology of Aging, 2017, vol. 49, p. 52-59
dc.relation.urihttps://doi.org/10.1016/j.neurobiolaging.2016.08.027
dc.rightscc-by-nc-nd (c) Elsevier B.V., 2017
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es
dc.sourceArticles publicats en revistes (Patologia i Terapèutica Experimental)
dc.subject.classificationMalaltia d'Alzheimer
dc.subject.classificationMetabolisme
dc.subject.classificationLòbul frontal
dc.subject.classificationCitologia
dc.subject.classificationDemència amb cossos de Lewy
dc.subject.classificationMetabolisme dels lípids
dc.subject.classificationTeixit nerviós
dc.subject.otherAlzheimer's disease
dc.subject.otherMetabolism
dc.subject.otherFrontal lobe
dc.subject.otherCytology
dc.subject.otherLewy body dementia
dc.subject.otherLipid metabolism
dc.subject.otherNerve tissue
dc.titleAnomalies occurring in lipid profiles and protein distribution in frontal cortex lipid rafts in dementia with Lewy bodies disclose neurochemical traits partially shared by Alzheimer's and Parkinson's diseases
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/acceptedVersion

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