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Disease-specific phenotypes in dopamine neurons from human iPS-based models of genetic and sporadic Parkinson's disease
Sánchez-Danés, Adriana; Richaud-Patin, Yvonne; Carballo Carbajal, Iria; Jiménez-Delgado, Senda; Caig, Carles; Mora, Sergio; Di Guglielmo, Claudia; Ezquerra, Mario; Patel, Bindiben; Giralt Torroella, Albert; Canals i Coll, Josep M.; Memo, Maurizio; Alberch i Vié, Jordi; López-Barneo, José; Vila Farré, Miquel; Cuervo, Ana Maria; Tolosa, Eduardo; Consiglio, Antonella; Raya Chamorro, Ángel
Induced pluripotent stem cells (iPSC) offer an unprecedented opportunity to model human disease in relevant cell types, but it is unclear whether they could successfully model age-related diseases such as Parkinson's disease (PD). Here, we generated iPSC lines from seven patients with idiopathic PD (ID-PD), four patients with familial PD associated to the G2019S mutation in the Leucine-Rich Repeat Kinase 2 (LRRK2) gene (LRRK2-PD) and four age- and sex-matched healthy individuals (Ctrl). Over long-time culture, dopaminergic neurons (DAn) differentiated from either ID-PD- or LRRK2-PD-iPSC showed morphological alterations, including reduced numbers of neurites and neurite arborization, as well as accumulation of autophagic vacuoles, which were not evident in DAn differentiated from Ctrl-iPSC. Further induction of autophagy and/or inhibition of lysosomal proteolysis greatly exacerbated the DAn morphological alterations, indicating autophagic compromise in DAn from ID-PD- and LRRK2-PD-iPSC, which we demonstrate occurs at the level of autophagosome clearance. Our study provides an iPSC-based in vitro model that captures the patients' genetic complexity and allows investigation of the pathogenesis of both sporadic and familial PD cases in a disease-relevant cell type.
-Dopamina
-Metabolisme
-Fenotip
-Genètica
-Neurones
-Malaltia de Parkinson
-Patologia
-Cèl·lules mare
-Dopamine
-Metabolism
-Phenotype
-Genetics
-Neurons
-Parkinson's disease
-Pathology
-Stem cells
(c) EMBO, 2012
Article
Article - Published version
EMBO Press
         

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Sánchez-Danés, Adriana; Richaud-Patin, Yvonne; Carballo-Carbajal, Iria; Jiménez-Delgado, Senda; Caig, Carles; Mora, Sergio; Di Guglielmo, Claudia; Ezquerra, Mario; Patel, Bindiben; Giralt Torroella, Albert; Canals i Coll, Josep M.; Memo, Maurizio; Alberch i Vié, Jordi; López-Barneo, José; Vila Farré, Miquel; Cuervo, Ana Maria; Tolosa, Eduardo; Consiglio, Antonella; Raya Chamorro, Ángel
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Domenico, Angelique Di; Carola, Giulia; Calatayud Aristoy, Carles; Pons-Espinal, Meritxell; Muñoz, Juan Pablo; Richaud-Patin, Yvonne; Fernandez-Carasa, Irene; Gut, Marta; Faella, Armida; Parameswaran, Janani; Soriano i Fradera, Jordi; Ferrer, Isidro (Ferrer Abizanda); Tolosa, Eduardo; Zorzano Olarte, Antonio; Cuervo, Ana Maria; Raya Chamorro, Ángel; Consiglio, Antonella
Domenico, Angelique Di; Carola, Giulia; Calatayud Aristoy, Carles; Pons-Espinal, Meritxell; Muñoz, Juan Pablo; Richaud-Patin, Yvonne; Fernandez-Carasa, Irene; Gut, Marta; Faella, Armida; Parameswaran, Janani; Soriano i Fradera, Jordi; Ferrer, Isidro (Ferrer Abizanda); Tolosa, Eduardo; Zorzano Olarte, Antonio; Cuervo, Ana Maria; Raya Chamorro, Ángel; Consiglio, Antonella
 

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