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
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/47477
Ver los metadatos del registro completo
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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 |
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info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
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article |
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publishedVersion |
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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 |
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http://hdl.handle.net/11336/47477 |
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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 |
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eng |
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eng |
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application/pdf application/pdf |
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Pergamon-Elsevier Science Ltd |
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