Caloric restriction rescues yeast cells from alpha-synuclein toxicity through autophagic control of proteostasis

Bibliographic Details
Main Author: Marques, Maria Belém Sousa Sampaio
Publication Date: 2018
Other Authors: Pereira, Hélder Filipe Carvalho, Santos, Ana R., Teixeira, Alexandra, Ludovico, Paula
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: http://hdl.handle.net/1822/58784
Summary: α-Synuclein (SNCA) is a presynaptic protein that is associated with the pathophysiology of synucleinopathies, including Parkinson's disease. SNCA is a naturally aggregation-prone protein, which may be degraded by the ubiquitin-proteasome system (UPS) and by lysosomal degradation pathways. Besides being a target of the proteolytic systems, SNCA can also alter the function of these pathways further, contributing to the progression of neurodegeneration. Deterioration of UPS and autophagy activities with aging further aggravates this toxic cycle. Caloric restriction (CR) is still the most effective non-genetic intervention promoting lifespan extension. It is known that CR-mediated lifespan extension is linked to the regulation of proteolytic systems, but the mechanisms underlying CR rescue of SNCA toxicity remain poorly understood. This study shows that CR balances UPS and autophagy activities during aging. CR enhances UPS activity, reversing the decline of the UPS activity promoted by SNCA, and keeps autophagy at homeostatic levels. Maintenance of autophagy at homeostatic levels appears to be relevant for UPS activity and for the mechanism underlying rescue of cells from SNCA-mediated toxicity by CR.
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spelling Caloric restriction rescues yeast cells from alpha-synuclein toxicity through autophagic control of proteostasiscaloric restrictionagingubiquitin-proteasome systemautophagyalpha-synucleinScience & Technologyα-Synuclein (SNCA) is a presynaptic protein that is associated with the pathophysiology of synucleinopathies, including Parkinson's disease. SNCA is a naturally aggregation-prone protein, which may be degraded by the ubiquitin-proteasome system (UPS) and by lysosomal degradation pathways. Besides being a target of the proteolytic systems, SNCA can also alter the function of these pathways further, contributing to the progression of neurodegeneration. Deterioration of UPS and autophagy activities with aging further aggravates this toxic cycle. Caloric restriction (CR) is still the most effective non-genetic intervention promoting lifespan extension. It is known that CR-mediated lifespan extension is linked to the regulation of proteolytic systems, but the mechanisms underlying CR rescue of SNCA toxicity remain poorly understood. This study shows that CR balances UPS and autophagy activities during aging. CR enhances UPS activity, reversing the decline of the UPS activity promoted by SNCA, and keeps autophagy at homeostatic levels. Maintenance of autophagy at homeostatic levels appears to be relevant for UPS activity and for the mechanism underlying rescue of cells from SNCA-mediated toxicity by CR.BSM and HP are supported by fellowships from the Fundação para a Ciência e Tecnologia (FCT, Portugal) (SFRH/BPD/90533/2012 and SFRH/BD/133087/2017, respectively).info:eu-repo/semantics/publishedVersionImpact Journals LLCUniversidade do MinhoMarques, Maria Belém Sousa SampaioPereira, Hélder Filipe CarvalhoSantos, Ana R.Teixeira, AlexandraLudovico, Paula20182018-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/1822/58784eng1945-458910.18632/aging.10167530530923info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2024-05-11T05:53:53Zoai:repositorium.sdum.uminho.pt:1822/58784Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T15:34:01.383535Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Caloric restriction rescues yeast cells from alpha-synuclein toxicity through autophagic control of proteostasis
title Caloric restriction rescues yeast cells from alpha-synuclein toxicity through autophagic control of proteostasis
spellingShingle Caloric restriction rescues yeast cells from alpha-synuclein toxicity through autophagic control of proteostasis
Marques, Maria Belém Sousa Sampaio
caloric restriction
aging
ubiquitin-proteasome system
autophagy
alpha-synuclein
Science & Technology
title_short Caloric restriction rescues yeast cells from alpha-synuclein toxicity through autophagic control of proteostasis
title_full Caloric restriction rescues yeast cells from alpha-synuclein toxicity through autophagic control of proteostasis
title_fullStr Caloric restriction rescues yeast cells from alpha-synuclein toxicity through autophagic control of proteostasis
title_full_unstemmed Caloric restriction rescues yeast cells from alpha-synuclein toxicity through autophagic control of proteostasis
title_sort Caloric restriction rescues yeast cells from alpha-synuclein toxicity through autophagic control of proteostasis
author Marques, Maria Belém Sousa Sampaio
author_facet Marques, Maria Belém Sousa Sampaio
Pereira, Hélder Filipe Carvalho
Santos, Ana R.
Teixeira, Alexandra
Ludovico, Paula
author_role author
author2 Pereira, Hélder Filipe Carvalho
Santos, Ana R.
Teixeira, Alexandra
Ludovico, Paula
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Marques, Maria Belém Sousa Sampaio
Pereira, Hélder Filipe Carvalho
Santos, Ana R.
Teixeira, Alexandra
Ludovico, Paula
dc.subject.por.fl_str_mv caloric restriction
aging
ubiquitin-proteasome system
autophagy
alpha-synuclein
Science & Technology
topic caloric restriction
aging
ubiquitin-proteasome system
autophagy
alpha-synuclein
Science & Technology
description α-Synuclein (SNCA) is a presynaptic protein that is associated with the pathophysiology of synucleinopathies, including Parkinson's disease. SNCA is a naturally aggregation-prone protein, which may be degraded by the ubiquitin-proteasome system (UPS) and by lysosomal degradation pathways. Besides being a target of the proteolytic systems, SNCA can also alter the function of these pathways further, contributing to the progression of neurodegeneration. Deterioration of UPS and autophagy activities with aging further aggravates this toxic cycle. Caloric restriction (CR) is still the most effective non-genetic intervention promoting lifespan extension. It is known that CR-mediated lifespan extension is linked to the regulation of proteolytic systems, but the mechanisms underlying CR rescue of SNCA toxicity remain poorly understood. This study shows that CR balances UPS and autophagy activities during aging. CR enhances UPS activity, reversing the decline of the UPS activity promoted by SNCA, and keeps autophagy at homeostatic levels. Maintenance of autophagy at homeostatic levels appears to be relevant for UPS activity and for the mechanism underlying rescue of cells from SNCA-mediated toxicity by CR.
publishDate 2018
dc.date.none.fl_str_mv 2018
2018-01-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.language.iso.fl_str_mv eng
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dc.relation.none.fl_str_mv 1945-4589
10.18632/aging.101675
30530923
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dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Impact Journals LLC
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