Systematic compositional analysis of exosomal extracellular vesicles produced by cells undergoing apoptosis, necroptosis and ferroptosis.

Regulated cell death apoptosis comparative proteomics exosomes extracellular vesicles ferroptosis necroptosis rRNA methylation

Journal

Journal of extracellular vesicles
ISSN: 2001-3078
Titre abrégé: J Extracell Vesicles
Pays: United States
ID NLM: 101610479

Informations de publication

Date de publication:
Oct 2023
Historique:
received: 11 01 2023
accepted: 25 08 2023
medline: 2 11 2023
pubmed: 9 10 2023
entrez: 8 10 2023
Statut: ppublish

Résumé

Formation of extracellular vesicles (EVs) has emerged as a novel paradigm in cell-to-cell communication in health and disease. EVs are notably produced during cell death but it had remained unclear whether different modalities of regulated cell death (RCD) influence the biogenesis and composition of EVs. To this end, we performed a comparative analysis of steady-state (ssEVs) and cell death-associated EVs (cdEVs) following TNF-induced necroptosis (necEVs), anti-Fas-induced apoptosis (apoEVs), and ML162-induced ferroptosis (ferEVs) using the same cell line. For each RCD condition, we determined the biophysical and biochemical characteristics of the cell death-associated EVs (cdEVs), the protein cargo, and the presence of methylated ribosomal RNA. We found that the global protein content of all cdEVs was increased compared to steady-state EVs. Qualitatively, the isolated exosomal ssEVs and cdEVs, contained a largely overlapping protein cargo including some quantitative differences in particular proteins. All cdEVs were enriched for proteins involved in RNA splicing and nuclear export, and showed distinctive rRNA methylation patterns compared to ssEVs. Interestingly, necEVs and apoEVs, but strikingly not ferEVs, showed enrichment of proteins involved in ribosome biogenesis. Altogether, our work documents quantitative and qualitative differences between ssEVs and cdEVs.

Identifiants

pubmed: 37807017
doi: 10.1002/jev2.12365
pmc: PMC10560658
doi:

Substances chimiques

Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e12365

Informations de copyright

© 2023 The Authors. Journal of Extracellular Vesicles published by Wiley Periodicals LLC on behalf of International Society for Extracellular Vesicles.

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Auteurs

Benjamin Cappe (B)

Cell Death and Inflammation Unit, VIB Center for Inflammation Research, Ghent, Belgium.
Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.

Mike Vadi (M)

Cell Death and Inflammation Unit, VIB Center for Inflammation Research, Ghent, Belgium.
Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.

Eliza Sack (E)

RNA Molecular Biology, Fonds de la Recherche Scientifique (F.R.S./FNRS), Université libre de Bruxelles (ULB), Biopark campus, Gosselies, Belgium.

Ludivine Wacheul (L)

RNA Molecular Biology, Fonds de la Recherche Scientifique (F.R.S./FNRS), Université libre de Bruxelles (ULB), Biopark campus, Gosselies, Belgium.

Bruno Verstraeten (B)

Cell Death and Inflammation Unit, VIB Center for Inflammation Research, Ghent, Belgium.
Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.

Sara Dufour (S)

VIB-UGent Center for Medical Biotechnology, VIB, Ghent, Belgium.
Department of Biomolecular Medicine, Ghent University, Ghent, Belgium.
VIB Proteomics Core, VIB, Ghent, Belgium.

Julien Franck (J)

University of Lille, Inserm U1192-Laboratoire Protéomique Réponse Inflammatoire Spectrométrie de Masse-PRISM, Lille, France.

Wei Xie (W)

Cell Death and Inflammation Unit, VIB Center for Inflammation Research, Ghent, Belgium.
Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.

Francis Impens (F)

VIB-UGent Center for Medical Biotechnology, VIB, Ghent, Belgium.
Department of Biomolecular Medicine, Ghent University, Ghent, Belgium.
VIB Proteomics Core, VIB, Ghent, Belgium.

An Hendrix (A)

Laboratory of Experimental Cancer Research, Department of Human Structure and Repair, Ghent University, Ghent, Belgium.

Denis L J Lafontaine (DLJ)

RNA Molecular Biology, Fonds de la Recherche Scientifique (F.R.S./FNRS), Université libre de Bruxelles (ULB), Biopark campus, Gosselies, Belgium.

Peter Vandenabeele (P)

Cell Death and Inflammation Unit, VIB Center for Inflammation Research, Ghent, Belgium.
Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.

Franck B Riquet (FB)

Cell Death and Inflammation Unit, VIB Center for Inflammation Research, Ghent, Belgium.
Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.
University of Lille, CNRS, UMR 8523-PhLAM-Physique des Lasers Atomes et Molécules, Lille, France.

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