Mesenchymal stem cells-derived exosomes: A new possible therapeutic strategy for Parkinson’s disease?
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/1822/60932 |
Resumo: | Parkinson’s disease (PD) is the second most prevalent neurodegenerative disorder worldwide. Clinically, it is characterized by severe motor complications caused by a progressive degeneration of dopaminergic neurons (DAn) and dopamine loss. Current treatment is focused on mitigating the symptoms through administration of levodopa, rather than on preventing DAn damage. Therefore, the use and development of neuroprotective/disease-modifying strategies is an absolute need, which can lead to promising gains on PD translational research. Mesenchymal stem cells (MSCs)–derived exosomes have been proposed as a promising therapeutic tool, since it has been demonstrated that they can act as biological nanoparticles with beneficial effects in different pathological conditions, including PD. Thus, considering their potential protective action in lesioned sites, MSCs-derived exosomes might also be active modulators of the neuroregeneration processes, opening a door for their future use as therapeutical strategies in human clinical trials. Therefore, in this review, we analyze the current understanding of MSCs-derived exosomes as a new possible therapeutic strategy for PD, by providing an overview about the potential role of miRNAs in the cellular and molecular basis of PD. |
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Mesenchymal stem cells-derived exosomes: A new possible therapeutic strategy for Parkinson’s disease?mesenchymal stem cellssecretomeexosomesParkinson's diseasemicroRNAsScience & TechnologyParkinson’s disease (PD) is the second most prevalent neurodegenerative disorder worldwide. Clinically, it is characterized by severe motor complications caused by a progressive degeneration of dopaminergic neurons (DAn) and dopamine loss. Current treatment is focused on mitigating the symptoms through administration of levodopa, rather than on preventing DAn damage. Therefore, the use and development of neuroprotective/disease-modifying strategies is an absolute need, which can lead to promising gains on PD translational research. Mesenchymal stem cells (MSCs)–derived exosomes have been proposed as a promising therapeutic tool, since it has been demonstrated that they can act as biological nanoparticles with beneficial effects in different pathological conditions, including PD. Thus, considering their potential protective action in lesioned sites, MSCs-derived exosomes might also be active modulators of the neuroregeneration processes, opening a door for their future use as therapeutical strategies in human clinical trials. Therefore, in this review, we analyze the current understanding of MSCs-derived exosomes as a new possible therapeutic strategy for PD, by providing an overview about the potential role of miRNAs in the cellular and molecular basis of PD.This research was funded by Portuguese Foundation for Science and Technology(FCT): IF Development Grant (IF/00111/2013) to AJ Salgado) and Post-Doctoral Fellowship to F.G. Teixeira (SFRH/BPD/118408/2016). This article has been developed under the scope of the project NORTE-01-0145-FEDER-000023, supported by the Northern Portugal Regional Operational Programme (NORTE 2020), under the Portugal 2020 Partnership Agreement, through the European Regional Development Fund (FEDER). This work has been funded by FEDER funds, through the Competitiveness Internationalization Operational Programme (POCI), and by National funds, through FCT, under the scope of the projects POCI-01-0145-FEDER-007038 and POCI-01-0145-FEDER-029751.info:eu-repo/semantics/publishedVersionMultidisciplinary Digital Publishing InstituteUniversidade do MinhoVilaça-Faria, HelenaSalgado, A. J.Teixeira, Fábio Gabriel Rodrigues2019-02-022019-02-02T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/1822/60932eng2073-440910.3390/cells8020118info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-21T12:37:09Zoai:repositorium.sdum.uminho.pt:1822/60932Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T19:33:24.084657Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Mesenchymal stem cells-derived exosomes: A new possible therapeutic strategy for Parkinson’s disease? |
title |
Mesenchymal stem cells-derived exosomes: A new possible therapeutic strategy for Parkinson’s disease? |
spellingShingle |
Mesenchymal stem cells-derived exosomes: A new possible therapeutic strategy for Parkinson’s disease? Vilaça-Faria, Helena mesenchymal stem cells secretome exosomes Parkinson's disease microRNAs Science & Technology |
title_short |
Mesenchymal stem cells-derived exosomes: A new possible therapeutic strategy for Parkinson’s disease? |
title_full |
Mesenchymal stem cells-derived exosomes: A new possible therapeutic strategy for Parkinson’s disease? |
title_fullStr |
Mesenchymal stem cells-derived exosomes: A new possible therapeutic strategy for Parkinson’s disease? |
title_full_unstemmed |
Mesenchymal stem cells-derived exosomes: A new possible therapeutic strategy for Parkinson’s disease? |
title_sort |
Mesenchymal stem cells-derived exosomes: A new possible therapeutic strategy for Parkinson’s disease? |
author |
Vilaça-Faria, Helena |
author_facet |
Vilaça-Faria, Helena Salgado, A. J. Teixeira, Fábio Gabriel Rodrigues |
author_role |
author |
author2 |
Salgado, A. J. Teixeira, Fábio Gabriel Rodrigues |
author2_role |
author author |
dc.contributor.none.fl_str_mv |
Universidade do Minho |
dc.contributor.author.fl_str_mv |
Vilaça-Faria, Helena Salgado, A. J. Teixeira, Fábio Gabriel Rodrigues |
dc.subject.por.fl_str_mv |
mesenchymal stem cells secretome exosomes Parkinson's disease microRNAs Science & Technology |
topic |
mesenchymal stem cells secretome exosomes Parkinson's disease microRNAs Science & Technology |
description |
Parkinson’s disease (PD) is the second most prevalent neurodegenerative disorder worldwide. Clinically, it is characterized by severe motor complications caused by a progressive degeneration of dopaminergic neurons (DAn) and dopamine loss. Current treatment is focused on mitigating the symptoms through administration of levodopa, rather than on preventing DAn damage. Therefore, the use and development of neuroprotective/disease-modifying strategies is an absolute need, which can lead to promising gains on PD translational research. Mesenchymal stem cells (MSCs)–derived exosomes have been proposed as a promising therapeutic tool, since it has been demonstrated that they can act as biological nanoparticles with beneficial effects in different pathological conditions, including PD. Thus, considering their potential protective action in lesioned sites, MSCs-derived exosomes might also be active modulators of the neuroregeneration processes, opening a door for their future use as therapeutical strategies in human clinical trials. Therefore, in this review, we analyze the current understanding of MSCs-derived exosomes as a new possible therapeutic strategy for PD, by providing an overview about the potential role of miRNAs in the cellular and molecular basis of PD. |
publishDate |
2019 |
dc.date.none.fl_str_mv |
2019-02-02 2019-02-02T00:00:00Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/1822/60932 |
url |
http://hdl.handle.net/1822/60932 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
2073-4409 10.3390/cells8020118 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Multidisciplinary Digital Publishing Institute |
publisher.none.fl_str_mv |
Multidisciplinary Digital Publishing Institute |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
repository.mail.fl_str_mv |
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1799132851655933952 |