Loss of SIRT2 leads to axonal degeneration and locomotor disability associated with redox and energy imbalance

ABSTRACT: Sirtuin 2 (SIRT2) is a member of a family of NAD+ -dependent histone deacetylases (HDAC) that play diverse roles in cellular metabolism and especially for aging process. SIRT2 is located in the nucleus, cytoplasm, and mitochondria, is highly expressed in the central nervous system (CNS), a...

Full description

Autores:
Ruiz Cortés, Zulma Tatiana
fourcade, Stéphane
Morató, Laia
Parameswaran, Janani
Ruiz, Montserrat
Jové, Ariona
Naudí, Alba
Martínez Redondo, Paloma
Dierssen, Mara
Ferrer, Isidre
Villarroya, Francesc
Pamplona, Reinald
Vaquero, Alejandro
Portero Otín, Manel
Pujol, Aurora
Tipo de recurso:
Article of investigation
Fecha de publicación:
2017
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/34420
Acceso en línea:
https://hdl.handle.net/10495/34420
Palabra clave:
Envejecimiento
Aging
Axones
Axons
ADN Mitocondrial
DNA, Mitochondrial
Metabolismo Energético
Energy Metabolism
Ratones
Mice
Ratones Endogámicos C57BL
Mice, Inbred C57BL
Ratones Noqueados
Mice, Knockout
Sirtuinas 2
Sirtuins 2
Enfermedades Neurodegenerativas
Neurodegenerative Diseases
Rights
openAccess
License
https://creativecommons.org/licenses/by/4.0/
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oai_identifier_str oai:bibliotecadigital.udea.edu.co:10495/34420
network_acronym_str UDEA2
network_name_str Repositorio UdeA
repository_id_str
dc.title.spa.fl_str_mv Loss of SIRT2 leads to axonal degeneration and locomotor disability associated with redox and energy imbalance
title Loss of SIRT2 leads to axonal degeneration and locomotor disability associated with redox and energy imbalance
spellingShingle Loss of SIRT2 leads to axonal degeneration and locomotor disability associated with redox and energy imbalance
Envejecimiento
Aging
Axones
Axons
ADN Mitocondrial
DNA, Mitochondrial
Metabolismo Energético
Energy Metabolism
Ratones
Mice
Ratones Endogámicos C57BL
Mice, Inbred C57BL
Ratones Noqueados
Mice, Knockout
Sirtuinas 2
Sirtuins 2
Enfermedades Neurodegenerativas
Neurodegenerative Diseases
title_short Loss of SIRT2 leads to axonal degeneration and locomotor disability associated with redox and energy imbalance
title_full Loss of SIRT2 leads to axonal degeneration and locomotor disability associated with redox and energy imbalance
title_fullStr Loss of SIRT2 leads to axonal degeneration and locomotor disability associated with redox and energy imbalance
title_full_unstemmed Loss of SIRT2 leads to axonal degeneration and locomotor disability associated with redox and energy imbalance
title_sort Loss of SIRT2 leads to axonal degeneration and locomotor disability associated with redox and energy imbalance
dc.creator.fl_str_mv Ruiz Cortés, Zulma Tatiana
fourcade, Stéphane
Morató, Laia
Parameswaran, Janani
Ruiz, Montserrat
Jové, Ariona
Naudí, Alba
Martínez Redondo, Paloma
Dierssen, Mara
Ferrer, Isidre
Villarroya, Francesc
Pamplona, Reinald
Vaquero, Alejandro
Portero Otín, Manel
Pujol, Aurora
dc.contributor.author.none.fl_str_mv Ruiz Cortés, Zulma Tatiana
fourcade, Stéphane
Morató, Laia
Parameswaran, Janani
Ruiz, Montserrat
Jové, Ariona
Naudí, Alba
Martínez Redondo, Paloma
Dierssen, Mara
Ferrer, Isidre
Villarroya, Francesc
Pamplona, Reinald
Vaquero, Alejandro
Portero Otín, Manel
Pujol, Aurora
dc.contributor.researchgroup.spa.fl_str_mv Biogénesis
dc.subject.decs.none.fl_str_mv Envejecimiento
Aging
Axones
Axons
ADN Mitocondrial
DNA, Mitochondrial
Metabolismo Energético
Energy Metabolism
Ratones
Mice
Ratones Endogámicos C57BL
Mice, Inbred C57BL
Ratones Noqueados
Mice, Knockout
Sirtuinas 2
Sirtuins 2
Enfermedades Neurodegenerativas
Neurodegenerative Diseases
topic Envejecimiento
Aging
Axones
Axons
ADN Mitocondrial
DNA, Mitochondrial
Metabolismo Energético
Energy Metabolism
Ratones
Mice
Ratones Endogámicos C57BL
Mice, Inbred C57BL
Ratones Noqueados
Mice, Knockout
Sirtuinas 2
Sirtuins 2
Enfermedades Neurodegenerativas
Neurodegenerative Diseases
description ABSTRACT: Sirtuin 2 (SIRT2) is a member of a family of NAD+ -dependent histone deacetylases (HDAC) that play diverse roles in cellular metabolism and especially for aging process. SIRT2 is located in the nucleus, cytoplasm, and mitochondria, is highly expressed in the central nervous system (CNS), and has been reported to regulate a variety of processes including oxidative stress, genome integrity, and myelination. However, little is known about the role of SIRT2 in the nervous system specifically during aging. Here, we show that middle-aged, 13-month-old mice lacking SIRT2 exhibit locomotor dysfunction due to axonal degeneration, which was not present in young SIRT2 mice. In addition, these Sirt2 / mice exhibit mitochondrial depletion resulting in energy failure, and redox dyshomeostasis. Our results provide a novel link between SIRT2 and physiological aging impacting the axonal compartment of the central nervous system, while supporting a major role for SIRT2 in orchestrating its metabolic regulation. This underscores the value of SIRT2 as a therapeutic target in the most prevalent neurodegenerative diseases that undergo with axonal degeneration associated with redox and energetic dyshomeostasis. Key words: aging; axonal degeneration; mitochondria; redox dyshomeostasis; sirtuin.
publishDate 2017
dc.date.issued.none.fl_str_mv 2017
dc.date.accessioned.none.fl_str_mv 2023-04-01T20:30:19Z
dc.date.available.none.fl_str_mv 2023-04-01T20:30:19Z
dc.type.spa.fl_str_mv Artículo de investigación
dc.type.coar.spa.fl_str_mv http://purl.org/coar/resource_type/c_2df8fbb1
dc.type.redcol.spa.fl_str_mv https://purl.org/redcol/resource_type/ART
dc.type.coarversion.spa.fl_str_mv http://purl.org/coar/version/c_970fb48d4fbd8a85
dc.type.driver.spa.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.citation.spa.fl_str_mv Fourcade S, Morató L, Parameswaran J, Ruiz M, Ruiz-Cortés T, Jové M, Naudí A, Martínez-Redondo P, Dierssen M, Ferrer I, Villarroya F, Pamplona R, Vaquero A, Portero-Otín M, Pujol A. Loss of SIRT2 leads to axonal degeneration and locomotor disability associated with redox and energy imbalance. Aging Cell. 2017 Dec;16(6):1404-1413. doi: 10.1111/acel.12682.
dc.identifier.issn.none.fl_str_mv 1474-9718
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/10495/34420
dc.identifier.doi.none.fl_str_mv 10.1111/acel.12682
dc.identifier.eissn.none.fl_str_mv 1474-9726
identifier_str_mv Fourcade S, Morató L, Parameswaran J, Ruiz M, Ruiz-Cortés T, Jové M, Naudí A, Martínez-Redondo P, Dierssen M, Ferrer I, Villarroya F, Pamplona R, Vaquero A, Portero-Otín M, Pujol A. Loss of SIRT2 leads to axonal degeneration and locomotor disability associated with redox and energy imbalance. Aging Cell. 2017 Dec;16(6):1404-1413. doi: 10.1111/acel.12682.
1474-9718
10.1111/acel.12682
1474-9726
url https://hdl.handle.net/10495/34420
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv Aging Cell.
dc.relation.citationendpage.spa.fl_str_mv 1413
dc.relation.citationissue.spa.fl_str_mv 6
dc.relation.citationstartpage.spa.fl_str_mv 1404
dc.relation.citationvolume.spa.fl_str_mv 16
dc.relation.ispartofjournal.spa.fl_str_mv Aging Cell
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dc.publisher.spa.fl_str_mv Wiley
dc.publisher.place.spa.fl_str_mv Oxford, Inglaterra
dc.publisher.faculty.spa.fl_str_mv sin facultad - programa
institution Universidad de Antioquia
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spelling Ruiz Cortés, Zulma Tatianafourcade, StéphaneMorató, LaiaParameswaran, JananiRuiz, MontserratJové, ArionaNaudí, AlbaMartínez Redondo, PalomaDierssen, MaraFerrer, IsidreVillarroya, FrancescPamplona, ReinaldVaquero, AlejandroPortero Otín, ManelPujol, AuroraBiogénesis2023-04-01T20:30:19Z2023-04-01T20:30:19Z2017Fourcade S, Morató L, Parameswaran J, Ruiz M, Ruiz-Cortés T, Jové M, Naudí A, Martínez-Redondo P, Dierssen M, Ferrer I, Villarroya F, Pamplona R, Vaquero A, Portero-Otín M, Pujol A. Loss of SIRT2 leads to axonal degeneration and locomotor disability associated with redox and energy imbalance. Aging Cell. 2017 Dec;16(6):1404-1413. doi: 10.1111/acel.12682.1474-9718https://hdl.handle.net/10495/3442010.1111/acel.126821474-9726ABSTRACT: Sirtuin 2 (SIRT2) is a member of a family of NAD+ -dependent histone deacetylases (HDAC) that play diverse roles in cellular metabolism and especially for aging process. SIRT2 is located in the nucleus, cytoplasm, and mitochondria, is highly expressed in the central nervous system (CNS), and has been reported to regulate a variety of processes including oxidative stress, genome integrity, and myelination. However, little is known about the role of SIRT2 in the nervous system specifically during aging. Here, we show that middle-aged, 13-month-old mice lacking SIRT2 exhibit locomotor dysfunction due to axonal degeneration, which was not present in young SIRT2 mice. In addition, these Sirt2 / mice exhibit mitochondrial depletion resulting in energy failure, and redox dyshomeostasis. Our results provide a novel link between SIRT2 and physiological aging impacting the axonal compartment of the central nervous system, while supporting a major role for SIRT2 in orchestrating its metabolic regulation. This underscores the value of SIRT2 as a therapeutic target in the most prevalent neurodegenerative diseases that undergo with axonal degeneration associated with redox and energetic dyshomeostasis. 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