Seminars In Cell And Developmental Biology

dc.creatorMarzolo MP
dc.creator, Bu G
dc.date2019-12-18T18:14:43Z
dc.date2022-07-07T22:03:05Z
dc.date2019-12-18T18:14:43Z
dc.date2022-07-07T22:03:05Z
dc.date2009
dc.date.accessioned2023-08-22T03:29:39Z
dc.date.available2023-08-22T03:29:39Z
dc.identifier13980001
dc.identifier13980001
dc.identifierhttps://hdl.handle.net/10533/237082
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/8315211
dc.descriptionAmyloid-beta (Abeta) peptide accumulation in the brain is central to the pathogenesis of Alzheimer's disease (AD). Abeta is produced through proteolytic processing of a transmembrane protein, beta-amyloid precursor protein (APP), by beta- and gamma-secretases. Mounting evidence has demonstrated that alterations in APP cellular trafficking and localization directly impact its processing to Abeta. Members of the low-density lipoprotein receptor family, including LRP, LRP1B, SorLA/LR11, and apoER2, interact with APP and regulate its endocytic trafficking. Additionally, APP trafficking and processing are greatly affected by cellular cholesterol content. In this review, we summarize the current understanding of the roles of lipoprotein receptors and cholesterol in APP trafficking and processing and their implication for AD pathogenesis and therapy.
dc.descriptionFONDAP
dc.descriptionFONDAP
dc.languageeng
dc.relationinstname: Conicyt
dc.relationreponame: Repositorio Digital RI2.0
dc.relationinfo:eu-repo/grantAgreement/Fondap/13980001
dc.relationhttps://www.ncbi.nlm.nih.gov/pubmed/19041409
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 Chile
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleLipoprotein receptors, cholesterol in APP trafficking and proteolytic processing, implications for Alzheimer’s disease
dc.titleSeminars In Cell And Developmental Biology
dc.typeArticulo
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion


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