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Portrait of blood-derived extracellular vesicles in patients with Parkinson's disease.
Lamontagne-Proulx, Jérôme; St-Amour, Isabelle; Labib, Richard; Pilon, Jérémie; Denis, Hélèna L; Cloutier, Nathalie; Roux-Dalvai, Florence; Vincent, Antony T; Mason, Sarah L; Williams-Gray, Caroline; Duchez, Anne-Claire; Droit, Arnaud; Lacroix, Steve; Dupré, Nicolas; Langlois, Mélanie; Chouinard, Sylvain; Panisset, Michel; Barker, Roger A; Boilard, Eric; Cicchetti, Francesca.
Afiliación
  • Lamontagne-Proulx J; Centre de recherche du CHU de Québec, Québec, QC, Canada.
  • St-Amour I; Centre de recherche du CHU de Québec, Québec, QC, Canada.
  • Labib R; Département de mathématiques et génie industriel, École Polytechnique de Montréal, Montréal, QC, Canada.
  • Pilon J; Département de mathématiques et génie industriel, École Polytechnique de Montréal, Montréal, QC, Canada.
  • Denis HL; Centre de recherche du CHU de Québec, Québec, QC, Canada.
  • Cloutier N; Centre de recherche du CHU de Québec, Québec, QC, Canada.
  • Roux-Dalvai F; Centre de recherche du CHU de Québec, Québec, QC, Canada.
  • Vincent AT; Institut de Biologie Intégrative et des Systèmes, Université Laval, Québec, QC, Canada.
  • Mason SL; Department of Clinical Neurosciences, John van Geest Centre for Brain Repair, University of Cambridge, Cambridge, United Kingdom.
  • Williams-Gray C; Department of Clinical Neurosciences, John van Geest Centre for Brain Repair, University of Cambridge, Cambridge, United Kingdom.
  • Duchez AC; Centre de recherche du CHU de Québec, Québec, QC, Canada.
  • Droit A; Centre de recherche du CHU de Québec, Québec, QC, Canada; Département de médecine moléculaire, Université Laval, Québec, QC, Canada.
  • Lacroix S; Centre de recherche du CHU de Québec, Québec, QC, Canada; Département de médecine moléculaire, Université Laval, Québec, QC, Canada.
  • Dupré N; Centre de recherche du CHU de Québec, Québec, QC, Canada; Département de médecine, Université Laval, Département de neurosciences, Hôpital de l'Enfant-Jésus, Québec, QC, Canada.
  • Langlois M; Centre de recherche du CHU de Québec, Québec, QC, Canada; Département de médecine, Université Laval, Département de neurosciences, Hôpital de l'Enfant-Jésus, Québec, QC, Canada.
  • Chouinard S; Centre Hospitalier de l'Université de Montréal and Centre de recherche du Centre Hospitalier de l'Université de Montréal, Hôpital Notre-Dame, Département de médicine, Université de Montréal, Montréal, QC, Canada.
  • Panisset M; Centre Hospitalier de l'Université de Montréal and Centre de recherche du Centre Hospitalier de l'Université de Montréal, Hôpital Notre-Dame, Département de médicine, Université de Montréal, Montréal, QC, Canada.
  • Barker RA; Department of Clinical Neurosciences, John van Geest Centre for Brain Repair, University of Cambridge, Cambridge, United Kingdom.
  • Boilard E; Centre de recherche du CHU de Québec, Québec, QC, Canada; Département de microbiologie-infectiologie et d'immunologie, Université Laval, Québec, QC, Canada. Electronic address: Eric.Boilard@crchudequebec.ulaval.ca.
  • Cicchetti F; Centre de recherche du CHU de Québec, Québec, QC, Canada; Département de psychiatrie & neurosciences, Université Laval, Québec, QC, Canada. Electronic address: Francesca.Cicchetti@crchudequebec.ulaval.ca.
Neurobiol Dis ; 124: 163-175, 2019 04.
Article en En | MEDLINE | ID: mdl-30408591
ABSTRACT
The production of extracellular vesicles (EV) is a ubiquitous feature of eukaryotic cells but pathological events can affect their formation and constituents. We sought to characterize the nature, profile and protein signature of EV in the plasma of Parkinson's disease (PD) patients and how they correlate to clinical measures of the disease. EV were initially collected from cohorts of PD (n = 60; Controls, n = 37) and Huntington's disease (HD) patients (Pre-manifest, n = 11; manifest, n = 52; Controls, n = 55) - for comparative purposes in individuals with another chronic neurodegenerative condition - and exhaustively analyzed using flow cytometry, electron microscopy and proteomics. We then collected 42 samples from an additional independent cohort of PD patients to confirm our initial results. Through a series of iterative steps, we optimized an approach for defining the EV signature in PD. We found that the number of EV derived specifically from erythrocytes segregated with UPDRS scores corresponding to different disease stages. Proteomic analysis further revealed that there is a specific signature of proteins that could reliably differentiate control subjects from mild and moderate PD patients. Taken together, we have developed/identified an EV blood-based assay that has the potential to be used as a biomarker for PD.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Eritrocitos / Vesículas Extracelulares Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Neurobiol Dis Asunto de la revista: NEUROLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Eritrocitos / Vesículas Extracelulares Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Neurobiol Dis Asunto de la revista: NEUROLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Canadá