Proteome profile of peripheral myelin in healthy mice and in a neuropathy model.


Journal

eLife
ISSN: 2050-084X
Titre abrégé: Elife
Pays: England
ID NLM: 101579614

Informations de publication

Date de publication:
04 03 2020
Historique:
received: 27 08 2019
accepted: 19 02 2020
entrez: 5 3 2020
pubmed: 5 3 2020
medline: 10 4 2021
Statut: epublish

Résumé

Proteome and transcriptome analyses aim at comprehending the molecular profiles of the brain, its cell-types and subcellular compartments including myelin. Despite the relevance of the peripheral nervous system for normal sensory and motor capabilities, analogous approaches to peripheral nerves and peripheral myelin have fallen behind evolving technical standards. Here we assess the peripheral myelin proteome by gel-free, label-free mass-spectrometry for deep quantitative coverage. Integration with RNA-Sequencing-based developmental mRNA-abundance profiles and neuropathy disease genes illustrates the utility of this resource. Notably, the periaxin-deficient mouse model of the neuropathy Charcot-Marie-Tooth 4F displays a highly pathological myelin proteome profile, exemplified by the discovery of reduced levels of the monocarboxylate transporter MCT1/SLC16A1 as a novel facet of the neuropathology. This work provides the most comprehensive proteome resource thus far to approach development, function and pathology of peripheral myelin, and a straightforward, accurate and sensitive workflow to address myelin diversity in health and disease.

Identifiants

pubmed: 32130108
doi: 10.7554/eLife.51406
pii: 51406
pmc: PMC7056269
doi:
pii:

Substances chimiques

Membrane Proteins 0
Myelin Proteins 0
Proteome 0
periaxin 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Deutsche Forschungsgemeinschaft
ID : WE 2720/2-2
Organisme : Deutsche Forschungsgemeinschaft
ID : WE 2720/4-1
Organisme : Deutsche Forschungsgemeinschaft
ID : WE 2720/5-1
Organisme : Deutsche Forschungsgemeinschaft
ID : RO 4076/3-2
Organisme : Wellcome
ID : 0842424

Informations de copyright

© 2020, Siems et al.

Déclaration de conflit d'intérêts

SS, OJ, ME, NK, LW, DS, KK, DH, RJ, RF, MS, MR, PB, HW No competing interests declared

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Auteurs

Sophie B Siems (SB)

Department of Neurogenetics, Max Planck Institute of Experimental Medicine, Göttingen, Germany.

Olaf Jahn (O)

Proteomics Group, Max Planck Institute of Experimental Medicine, Göttingen, Germany.

Maria A Eichel (MA)

Department of Neurogenetics, Max Planck Institute of Experimental Medicine, Göttingen, Germany.

Nirmal Kannaiyan (N)

Department of Psychiatry and Psychotherapy, University Hospital, LMU Munich, Munich, Germany.

Lai Man N Wu (LMN)

Centre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, United Kingdom.

Diane L Sherman (DL)

Centre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, United Kingdom.

Kathrin Kusch (K)

Department of Neurogenetics, Max Planck Institute of Experimental Medicine, Göttingen, Germany.

Dörte Hesse (D)

Proteomics Group, Max Planck Institute of Experimental Medicine, Göttingen, Germany.

Ramona B Jung (RB)

Department of Neurogenetics, Max Planck Institute of Experimental Medicine, Göttingen, Germany.

Robert Fledrich (R)

Department of Neurogenetics, Max Planck Institute of Experimental Medicine, Göttingen, Germany.
Institute of Anatomy, University of Leipzig, Leipzig, Germany.

Michael W Sereda (MW)

Department of Neurogenetics, Max Planck Institute of Experimental Medicine, Göttingen, Germany.
Department of Clinical Neurophysiology, University Medical Center, Göttingen, Germany.

Moritz J Rossner (MJ)

Department of Psychiatry and Psychotherapy, University Hospital, LMU Munich, Munich, Germany.

Peter J Brophy (PJ)

Centre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, United Kingdom.

Hauke B Werner (HB)

Department of Neurogenetics, Max Planck Institute of Experimental Medicine, Göttingen, Germany.

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