Extracellular Vesicles Physiological Role and the Particular Case of Disease-Spreading Mechanisms in Polyglutamine Diseases

Recent 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...

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Autores principales: Ricardo Moreira, Liliana S. Mendonça, Luís Pereira de Almeida
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Publicado: MDPI AG 2021
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spelling oai:doaj.org-article:a9746ba5c6a24757a36db0ba0819bcde2021-11-25T17:55:05ZExtracellular Vesicles Physiological Role and the Particular Case of Disease-Spreading Mechanisms in Polyglutamine Diseases10.3390/ijms2222122881422-00671661-6596https://doaj.org/article/a9746ba5c6a24757a36db0ba0819bcde2021-11-01T00:00:00Zhttps://www.mdpi.com/1422-0067/22/22/12288https://doaj.org/toc/1661-6596https://doaj.org/toc/1422-0067Recent 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.Ricardo MoreiraLiliana S. MendonçaLuís Pereira de AlmeidaMDPI AGarticleextracellular vesiclesdisease spreadingneurodegenerative diseasespolyglutamine diseasesvehiclebiomarkerBiology (General)QH301-705.5ChemistryQD1-999ENInternational Journal of Molecular Sciences, Vol 22, Iss 12288, p 12288 (2021)
institution DOAJ
collection DOAJ
language EN
topic extracellular vesicles
disease spreading
neurodegenerative diseases
polyglutamine diseases
vehicle
biomarker
Biology (General)
QH301-705.5
Chemistry
QD1-999
spellingShingle extracellular vesicles
disease spreading
neurodegenerative diseases
polyglutamine diseases
vehicle
biomarker
Biology (General)
QH301-705.5
Chemistry
QD1-999
Ricardo Moreira
Liliana S. Mendonça
Luís Pereira de Almeida
Extracellular Vesicles Physiological Role and the Particular Case of Disease-Spreading Mechanisms in Polyglutamine Diseases
description Recent 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.
format article
author Ricardo Moreira
Liliana S. Mendonça
Luís Pereira de Almeida
author_facet Ricardo Moreira
Liliana S. Mendonça
Luís Pereira de Almeida
author_sort Ricardo Moreira
title Extracellular Vesicles Physiological Role and the Particular Case of Disease-Spreading Mechanisms in Polyglutamine Diseases
title_short Extracellular Vesicles Physiological Role and the Particular Case of Disease-Spreading Mechanisms in Polyglutamine Diseases
title_full Extracellular Vesicles Physiological Role and the Particular Case of Disease-Spreading Mechanisms in Polyglutamine Diseases
title_fullStr Extracellular Vesicles Physiological Role and the Particular Case of Disease-Spreading Mechanisms in Polyglutamine Diseases
title_full_unstemmed Extracellular Vesicles Physiological Role and the Particular Case of Disease-Spreading Mechanisms in Polyglutamine Diseases
title_sort extracellular vesicles physiological role and the particular case of disease-spreading mechanisms in polyglutamine diseases
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/a9746ba5c6a24757a36db0ba0819bcde
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