Isotopic Evidence for Disrupted Copper Metabolism in Amyotrophic Lateral Sclerosis
Summary: Redox-active metals are thought to be implicated in neurodegenerative diseases including amyotrophic lateral sclerosis (ALS). To address this point, we measured the concentrations of 12 elements and, for the first time, the stable isotope compositions of copper (redox-active) and zinc (redo...
Main Authors: | , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2018-08-01
|
Series: | iScience |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2589004218301111 |
id |
doaj-43e5361b27b449fcba379df890dfe965 |
---|---|
record_format |
Article |
spelling |
doaj-43e5361b27b449fcba379df890dfe9652020-11-25T01:59:01ZengElsevieriScience2589-00422018-08-016264271Isotopic Evidence for Disrupted Copper Metabolism in Amyotrophic Lateral SclerosisLucie Sauzéat0Emilien Bernard1Armand Perret-Liaudet2Isabelle Quadrio3Alain Vighetto4Pierre Krolak-Salmon5Emmanuel Broussolle6Pascal Leblanc7Vincent Balter8Université de Lyon, ENS de Lyon, CNRS, LGL-TPE, 69007 Lyon, FranceHospices Civils de Lyon, Hôpital Neurologique Pierre Wertheimer, Centre de Ressources et de Compétence SLA de Lyon, Service de Neurologie C, Bron, FranceUniversité de Lyon, CNRS UMR5292, INSERM U1028, BioRan, Lyon, France; Hospices Civils de Lyon, Neurobiology Laboratory, Biochemistry and Molecular Biology Department, Lyon, FranceUniversité de Lyon, CNRS UMR5292, INSERM U1028, BioRan, Lyon, France; Hospices Civils de Lyon, Neurobiology Laboratory, Biochemistry and Molecular Biology Department, Lyon, FranceService Neurocognition et Neuroophtalmologie, Hôpital Neurologique, 59 Boulevard Pinel, 69677 Bron Cedex, France; Centre Mémoire Ressources Recherche de Lyon, Hospices Civils de Lyon, Hôpital des Charpennes, Villeurbanne, France; Université Lyon 1, Hospices Civils de Lyon, Centre de Recherche en Neurosciences de Lyon, équipe IMPACT, Lyon, FranceCentre Mémoire Ressources Recherche de Lyon, Hospices Civils de Lyon, Hôpital des Charpennes, Villeurbanne, FranceUniversité de Lyon, Faculté de Médecine Lyon Sud Charles Mérieux, Institut des Sciences Cognitives Marc Jeannerod, CNRS, UMR 5229, Lyon, FranceInstitut NeuroMyoGène, CNRS UMR5310, INSERM U1217, Faculté de Médecine Rockefeller, Université Claude Bernard Lyon I, 8 Avenue Rockefeller, 69373 Lyon Cedex 08, FranceUniversité de Lyon, ENS de Lyon, CNRS, LGL-TPE, 69007 Lyon, France; Corresponding authorSummary: Redox-active metals are thought to be implicated in neurodegenerative diseases including amyotrophic lateral sclerosis (ALS). To address this point, we measured the concentrations of 12 elements and, for the first time, the stable isotope compositions of copper (redox-active) and zinc (redox-inactive) in human cerebrospinal fluids of 31 patients with ALS, 11 age-matched controls (CTRL), and 14 patients with Alzheimer disease. We first show that metal concentrations weakly discriminate patients with ALS from the two other groups. We then report that zinc isotopic compositions are similar in the three groups, but that patients with ALS have significantly 65copper-enriched isotopic compositions relative to CTRL and patients with AD. This result unambiguously demonstrates that copper is implicated in ALS. We suggest that this copper isotopic signature may result from abnormal protein aggregation in the brain parenchyma, and propose that isotopic analysis is a potential tool that may help unraveling the molecular mechanisms at work in ALS. : Nuclear Medicine; Isotope Chemistry; Neuroscience; Clinical Neuroscience Subject Areas: Nuclear Medicine, Isotope Chemistry, Neuroscience, Clinical Neurosciencehttp://www.sciencedirect.com/science/article/pii/S2589004218301111 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Lucie Sauzéat Emilien Bernard Armand Perret-Liaudet Isabelle Quadrio Alain Vighetto Pierre Krolak-Salmon Emmanuel Broussolle Pascal Leblanc Vincent Balter |
spellingShingle |
Lucie Sauzéat Emilien Bernard Armand Perret-Liaudet Isabelle Quadrio Alain Vighetto Pierre Krolak-Salmon Emmanuel Broussolle Pascal Leblanc Vincent Balter Isotopic Evidence for Disrupted Copper Metabolism in Amyotrophic Lateral Sclerosis iScience |
author_facet |
Lucie Sauzéat Emilien Bernard Armand Perret-Liaudet Isabelle Quadrio Alain Vighetto Pierre Krolak-Salmon Emmanuel Broussolle Pascal Leblanc Vincent Balter |
author_sort |
Lucie Sauzéat |
title |
Isotopic Evidence for Disrupted Copper Metabolism in Amyotrophic Lateral Sclerosis |
title_short |
Isotopic Evidence for Disrupted Copper Metabolism in Amyotrophic Lateral Sclerosis |
title_full |
Isotopic Evidence for Disrupted Copper Metabolism in Amyotrophic Lateral Sclerosis |
title_fullStr |
Isotopic Evidence for Disrupted Copper Metabolism in Amyotrophic Lateral Sclerosis |
title_full_unstemmed |
Isotopic Evidence for Disrupted Copper Metabolism in Amyotrophic Lateral Sclerosis |
title_sort |
isotopic evidence for disrupted copper metabolism in amyotrophic lateral sclerosis |
publisher |
Elsevier |
series |
iScience |
issn |
2589-0042 |
publishDate |
2018-08-01 |
description |
Summary: Redox-active metals are thought to be implicated in neurodegenerative diseases including amyotrophic lateral sclerosis (ALS). To address this point, we measured the concentrations of 12 elements and, for the first time, the stable isotope compositions of copper (redox-active) and zinc (redox-inactive) in human cerebrospinal fluids of 31 patients with ALS, 11 age-matched controls (CTRL), and 14 patients with Alzheimer disease. We first show that metal concentrations weakly discriminate patients with ALS from the two other groups. We then report that zinc isotopic compositions are similar in the three groups, but that patients with ALS have significantly 65copper-enriched isotopic compositions relative to CTRL and patients with AD. This result unambiguously demonstrates that copper is implicated in ALS. We suggest that this copper isotopic signature may result from abnormal protein aggregation in the brain parenchyma, and propose that isotopic analysis is a potential tool that may help unraveling the molecular mechanisms at work in ALS. : Nuclear Medicine; Isotope Chemistry; Neuroscience; Clinical Neuroscience Subject Areas: Nuclear Medicine, Isotope Chemistry, Neuroscience, Clinical Neuroscience |
url |
http://www.sciencedirect.com/science/article/pii/S2589004218301111 |
work_keys_str_mv |
AT luciesauzeat isotopicevidencefordisruptedcoppermetabolisminamyotrophiclateralsclerosis AT emilienbernard isotopicevidencefordisruptedcoppermetabolisminamyotrophiclateralsclerosis AT armandperretliaudet isotopicevidencefordisruptedcoppermetabolisminamyotrophiclateralsclerosis AT isabellequadrio isotopicevidencefordisruptedcoppermetabolisminamyotrophiclateralsclerosis AT alainvighetto isotopicevidencefordisruptedcoppermetabolisminamyotrophiclateralsclerosis AT pierrekrolaksalmon isotopicevidencefordisruptedcoppermetabolisminamyotrophiclateralsclerosis AT emmanuelbroussolle isotopicevidencefordisruptedcoppermetabolisminamyotrophiclateralsclerosis AT pascalleblanc isotopicevidencefordisruptedcoppermetabolisminamyotrophiclateralsclerosis AT vincentbalter isotopicevidencefordisruptedcoppermetabolisminamyotrophiclateralsclerosis |
_version_ |
1724966387832586240 |