Cargando…

ATP13A2 and Alpha-synuclein: a Metal Taste in Autophagy

Parkinson's Disease (PD) is a complex and multifactorial disorder of both idiopathic and genetic origin. Thus far, more than 20 genes have been linked to familial forms of PD. Two of these genes encode for ATP13A2 and alpha-synuclein (asyn), proteins that seem to be members of a common network...

Descripción completa

Detalles Bibliográficos
Autores principales: Lopes da Fonseca, Tomás, Outeiro, Tiago Fleming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Brain and Neural Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4276802/
https://www.ncbi.nlm.nih.gov/pubmed/25548531
http://dx.doi.org/10.5607/en.2014.23.4.314
_version_ 1782350299938160640
author Lopes da Fonseca, Tomás
Outeiro, Tiago Fleming
author_facet Lopes da Fonseca, Tomás
Outeiro, Tiago Fleming
author_sort Lopes da Fonseca, Tomás
collection PubMed
description Parkinson's Disease (PD) is a complex and multifactorial disorder of both idiopathic and genetic origin. Thus far, more than 20 genes have been linked to familial forms of PD. Two of these genes encode for ATP13A2 and alpha-synuclein (asyn), proteins that seem to be members of a common network in both physiological and disease conditions. Thus, two different hypotheses have emerged supporting a role of ATP13A2 and asyn in metal homeostasis or in autophagy. Interestingly, an appealing theory might combine these two cellular pathways. Here we review the novel findings in the interaction between these two proteins and debate the exciting roads still ahead.
format Online
Article
Text
id pubmed-4276802
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher The Korean Society for Brain and Neural Science
record_format MEDLINE/PubMed
spelling pubmed-42768022014-12-29 ATP13A2 and Alpha-synuclein: a Metal Taste in Autophagy Lopes da Fonseca, Tomás Outeiro, Tiago Fleming Exp Neurobiol Review Article Parkinson's Disease (PD) is a complex and multifactorial disorder of both idiopathic and genetic origin. Thus far, more than 20 genes have been linked to familial forms of PD. Two of these genes encode for ATP13A2 and alpha-synuclein (asyn), proteins that seem to be members of a common network in both physiological and disease conditions. Thus, two different hypotheses have emerged supporting a role of ATP13A2 and asyn in metal homeostasis or in autophagy. Interestingly, an appealing theory might combine these two cellular pathways. Here we review the novel findings in the interaction between these two proteins and debate the exciting roads still ahead. The Korean Society for Brain and Neural Science 2014-12 2014-12-12 /pmc/articles/PMC4276802/ /pubmed/25548531 http://dx.doi.org/10.5607/en.2014.23.4.314 Text en Copyright © Experimental Neurobiology 2014. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Lopes da Fonseca, Tomás
Outeiro, Tiago Fleming
ATP13A2 and Alpha-synuclein: a Metal Taste in Autophagy
title ATP13A2 and Alpha-synuclein: a Metal Taste in Autophagy
title_full ATP13A2 and Alpha-synuclein: a Metal Taste in Autophagy
title_fullStr ATP13A2 and Alpha-synuclein: a Metal Taste in Autophagy
title_full_unstemmed ATP13A2 and Alpha-synuclein: a Metal Taste in Autophagy
title_short ATP13A2 and Alpha-synuclein: a Metal Taste in Autophagy
title_sort atp13a2 and alpha-synuclein: a metal taste in autophagy
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4276802/
https://www.ncbi.nlm.nih.gov/pubmed/25548531
http://dx.doi.org/10.5607/en.2014.23.4.314
work_keys_str_mv AT lopesdafonsecatomas atp13a2andalphasynucleinametaltasteinautophagy
AT outeirotiagofleming atp13a2andalphasynucleinametaltasteinautophagy