Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/104803
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dc.contributor.authorMoreira, Ricardo-
dc.contributor.authorMendonça, Liliana Simões-
dc.contributor.authorAlmeida, Luís Pereira de-
dc.date.accessioned2023-01-25T10:43:00Z-
dc.date.available2023-01-25T10:43:00Z-
dc.date.issued2021-11-13-
dc.identifier.issn1422-0067pt
dc.identifier.urihttps://hdl.handle.net/10316/104803-
dc.description.abstractRecent research demonstrated pathological spreading of the disease-causing proteins from one focal point across other brain regions for some neurodegenerative diseases, such as Parkinson's and Alzheimer's disease. Spreading mediated by extracellular vesicles is one of the proposed disease-spreading mechanisms. Extracellular vesicles are cell membrane-derived vesicles, used by cells for cell-to-cell communication and excretion of toxic components. Importantly, extracellular vesicles carrying pathological molecules, when internalized by "healthy" cells, may trigger pathological pathways and, consequently, promote disease spreading to neighboring cells. Polyglutamine diseases are a group of genetic neurodegenerative disorders characterized by the accumulation of mutant misfolded proteins carrying an expanded tract of glutamines, including Huntington's and Machado-Joseph disease. The pathological spread of the misfolded proteins or the corresponding mutant mRNA has been explored. The understanding of the disease-spreading mechanism that plays a key role in the pathology progression of these diseases can result in the development of effective therapeutic approaches to stop disease progression, arresting the spread of the toxic components and disease aggravation. Therefore, the present review's main focus is the disease-spreading mechanisms with emphasis on polyglutamine diseases and the putative role played by extracellular vesicles in this process.pt
dc.language.isoengpt
dc.publisherMDPIpt
dc.relationCENTRO-01- 0145-FEDER-000008pt
dc.relationUIDB/04539/2020pt
dc.relationPOCI-01-0145-FEDER-030737pt
dc.relationPTDC/BTM-ORG/30737/2017pt
dc.relationCEECIND/04242/2017pt
dc.relationPhD Scholarship 2020.04751.BDpt
dc.relationNational Ataxia Foundationpt
dc.relationFrench Muscular Dystrophy Association (AFM-Téléthon) Trampoline Grant #20126pt
dc.relationRichard Chin and Lily Lock Machado–Joseph Disease Research Fundpt
dc.relationJPND project SynSpreadpt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subjectextracellular vesicles;pt
dc.subjectdisease spreading;pt
dc.subjectneurodegenerative diseases;pt
dc.subjectpolyglutamine diseases;pt
dc.subjectvehicle;pt
dc.subjectbiomarkerpt
dc.subject.meshAnimalspt
dc.subject.meshHumanspt
dc.subject.meshPeptidespt
dc.subject.meshExtracellular Vesiclespt
dc.subject.meshHuntington Diseasept
dc.subject.meshMachado-Joseph Diseasept
dc.titleExtracellular Vesicles Physiological Role and the Particular Case of Disease-Spreading Mechanisms in Polyglutamine Diseasespt
dc.typearticle-
degois.publication.firstPage12288pt
degois.publication.issue22pt
degois.publication.titleInternational Journal of Molecular Sciencespt
dc.peerreviewedyespt
dc.identifier.doi10.3390/ijms222212288pt
degois.publication.volume22pt
dc.date.embargo2021-11-13*
uc.date.periodoEmbargo0pt
item.grantfulltextopen-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.openairetypearticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextCom Texto completo-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.researchunitCIBB - Center for Innovative Biomedicine and Biotechnology-
crisitem.author.orcid0000-0002-0218-9690-
crisitem.author.orcid0000-0001-5831-3307-
Appears in Collections:I&D CNC - Artigos em Revistas Internacionais
I&D CIBB - Artigos em Revistas Internacionais
FFUC- Artigos em Revistas Internacionais
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