The strategic function of the P5-ATPase ATP13A2 in toxic waste disposal

Autores
de Tezanos Pinto, Felicitas; Adamo, Hugo Pedro
Año de publicación
2017
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The P-type ATPase ATP13A2 protein was originally associated with a form of Parkinson´s Disease (PD)known as Kufor Rakeb Syndrome (KRS). However, in the last years it has been found to underlay variantsof neuronal ceroid-lipofuscinoses and hereditary spastic paraplegia. These findings expand the clinicaland genetic spectrum of ATP13A2-associated disorders, which are commonly characterized by lysosomaldysfunction. Nowadays it is well known that lysosomes are not merely related to the degradation andrecycling of cellular waste, but are also involved in fundamental processes such as secretion, plasmamembrane repair, signaling, energy metabolism and autophagy. The essential role of lysosomes in thesecellular processes has significant implications for health and disease. ATP13A2 is localized in lysosomesand late endosomes and its mutation leads to lysosome dysfunction, diminishes the exosome secretionand impairs autophagic flux. In this review, we first describe ATP13A2-associated disorders and theirrelation with the endolysosomal pathway. We then describe the ATP13A2-involvement in iron homeostasisand its potential linkage with new pathologies like cancer, and finally, we consider the putativerole of ATP13A2 in lipid processing and degradation, opening the interesting possibility of a broader roleof this protein providing protection against a variety of disease-associated changes affecting cellularhomeostasis.
Fil: de Tezanos Pinto, Felicitas. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Química y Físico-Química Biológicas ; Argentina
Fil: Adamo, Hugo Pedro. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Química y Físico-Química Biológicas ; Argentina
Materia
P5-Atpase
Atp13a2
Parkinson'S Disease
Neuronal Ceroid Lipofuscinosis
Endolysosomal Pathway
Lysosome Degradation
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/47477

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network_name_str CONICET Digital (CONICET)
spelling The strategic function of the P5-ATPase ATP13A2 in toxic waste disposalde Tezanos Pinto, FelicitasAdamo, Hugo PedroP5-AtpaseAtp13a2Parkinson'S DiseaseNeuronal Ceroid LipofuscinosisEndolysosomal PathwayLysosome Degradationhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1The P-type ATPase ATP13A2 protein was originally associated with a form of Parkinson´s Disease (PD)known as Kufor Rakeb Syndrome (KRS). However, in the last years it has been found to underlay variantsof neuronal ceroid-lipofuscinoses and hereditary spastic paraplegia. These findings expand the clinicaland genetic spectrum of ATP13A2-associated disorders, which are commonly characterized by lysosomaldysfunction. Nowadays it is well known that lysosomes are not merely related to the degradation andrecycling of cellular waste, but are also involved in fundamental processes such as secretion, plasmamembrane repair, signaling, energy metabolism and autophagy. The essential role of lysosomes in thesecellular processes has significant implications for health and disease. ATP13A2 is localized in lysosomesand late endosomes and its mutation leads to lysosome dysfunction, diminishes the exosome secretionand impairs autophagic flux. In this review, we first describe ATP13A2-associated disorders and theirrelation with the endolysosomal pathway. We then describe the ATP13A2-involvement in iron homeostasisand its potential linkage with new pathologies like cancer, and finally, we consider the putativerole of ATP13A2 in lipid processing and degradation, opening the interesting possibility of a broader roleof this protein providing protection against a variety of disease-associated changes affecting cellularhomeostasis.Fil: de Tezanos Pinto, Felicitas. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Química y Físico-Química Biológicas ; ArgentinaFil: Adamo, Hugo Pedro. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Química y Físico-Química Biológicas ; ArgentinaPergamon-Elsevier Science Ltd2017-11info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/47477de Tezanos Pinto, Felicitas; Adamo, Hugo Pedro; The strategic function of the P5-ATPase ATP13A2 in toxic waste disposal; Pergamon-Elsevier Science Ltd; Neurochemistry International; 112; 11-2017; 108-1130197-0186CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1016/j.neuint.2017.11.008info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0197018617303017info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-22T11:03:41Zoai:ri.conicet.gov.ar:11336/47477instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-10-22 11:03:41.484CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv The strategic function of the P5-ATPase ATP13A2 in toxic waste disposal
title The strategic function of the P5-ATPase ATP13A2 in toxic waste disposal
spellingShingle The strategic function of the P5-ATPase ATP13A2 in toxic waste disposal
de Tezanos Pinto, Felicitas
P5-Atpase
Atp13a2
Parkinson'S Disease
Neuronal Ceroid Lipofuscinosis
Endolysosomal Pathway
Lysosome Degradation
title_short The strategic function of the P5-ATPase ATP13A2 in toxic waste disposal
title_full The strategic function of the P5-ATPase ATP13A2 in toxic waste disposal
title_fullStr The strategic function of the P5-ATPase ATP13A2 in toxic waste disposal
title_full_unstemmed The strategic function of the P5-ATPase ATP13A2 in toxic waste disposal
title_sort The strategic function of the P5-ATPase ATP13A2 in toxic waste disposal
dc.creator.none.fl_str_mv de Tezanos Pinto, Felicitas
Adamo, Hugo Pedro
author de Tezanos Pinto, Felicitas
author_facet de Tezanos Pinto, Felicitas
Adamo, Hugo Pedro
author_role author
author2 Adamo, Hugo Pedro
author2_role author
dc.subject.none.fl_str_mv P5-Atpase
Atp13a2
Parkinson'S Disease
Neuronal Ceroid Lipofuscinosis
Endolysosomal Pathway
Lysosome Degradation
topic P5-Atpase
Atp13a2
Parkinson'S Disease
Neuronal Ceroid Lipofuscinosis
Endolysosomal Pathway
Lysosome Degradation
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv The P-type ATPase ATP13A2 protein was originally associated with a form of Parkinson´s Disease (PD)known as Kufor Rakeb Syndrome (KRS). However, in the last years it has been found to underlay variantsof neuronal ceroid-lipofuscinoses and hereditary spastic paraplegia. These findings expand the clinicaland genetic spectrum of ATP13A2-associated disorders, which are commonly characterized by lysosomaldysfunction. Nowadays it is well known that lysosomes are not merely related to the degradation andrecycling of cellular waste, but are also involved in fundamental processes such as secretion, plasmamembrane repair, signaling, energy metabolism and autophagy. The essential role of lysosomes in thesecellular processes has significant implications for health and disease. ATP13A2 is localized in lysosomesand late endosomes and its mutation leads to lysosome dysfunction, diminishes the exosome secretionand impairs autophagic flux. In this review, we first describe ATP13A2-associated disorders and theirrelation with the endolysosomal pathway. We then describe the ATP13A2-involvement in iron homeostasisand its potential linkage with new pathologies like cancer, and finally, we consider the putativerole of ATP13A2 in lipid processing and degradation, opening the interesting possibility of a broader roleof this protein providing protection against a variety of disease-associated changes affecting cellularhomeostasis.
Fil: de Tezanos Pinto, Felicitas. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Química y Físico-Química Biológicas ; Argentina
Fil: Adamo, Hugo Pedro. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Química y Físico-Química Biológicas ; Argentina
description The P-type ATPase ATP13A2 protein was originally associated with a form of Parkinson´s Disease (PD)known as Kufor Rakeb Syndrome (KRS). However, in the last years it has been found to underlay variantsof neuronal ceroid-lipofuscinoses and hereditary spastic paraplegia. These findings expand the clinicaland genetic spectrum of ATP13A2-associated disorders, which are commonly characterized by lysosomaldysfunction. Nowadays it is well known that lysosomes are not merely related to the degradation andrecycling of cellular waste, but are also involved in fundamental processes such as secretion, plasmamembrane repair, signaling, energy metabolism and autophagy. The essential role of lysosomes in thesecellular processes has significant implications for health and disease. ATP13A2 is localized in lysosomesand late endosomes and its mutation leads to lysosome dysfunction, diminishes the exosome secretionand impairs autophagic flux. In this review, we first describe ATP13A2-associated disorders and theirrelation with the endolysosomal pathway. We then describe the ATP13A2-involvement in iron homeostasisand its potential linkage with new pathologies like cancer, and finally, we consider the putativerole of ATP13A2 in lipid processing and degradation, opening the interesting possibility of a broader roleof this protein providing protection against a variety of disease-associated changes affecting cellularhomeostasis.
publishDate 2017
dc.date.none.fl_str_mv 2017-11
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/47477
de Tezanos Pinto, Felicitas; Adamo, Hugo Pedro; The strategic function of the P5-ATPase ATP13A2 in toxic waste disposal; Pergamon-Elsevier Science Ltd; Neurochemistry International; 112; 11-2017; 108-113
0197-0186
CONICET Digital
CONICET
url http://hdl.handle.net/11336/47477
identifier_str_mv de Tezanos Pinto, Felicitas; Adamo, Hugo Pedro; The strategic function of the P5-ATPase ATP13A2 in toxic waste disposal; Pergamon-Elsevier Science Ltd; Neurochemistry International; 112; 11-2017; 108-113
0197-0186
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.1016/j.neuint.2017.11.008
info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0197018617303017
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Pergamon-Elsevier Science Ltd
publisher.none.fl_str_mv Pergamon-Elsevier Science Ltd
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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