Evoked Weibel-Palade Body Exocytosis Modifies the Endothelial Cell Surface by Releasing a Substrate-Selective Phosphodiesterase.

GPI anchor calcium complement inflammation secretion

Journal

Advanced science (Weinheim, Baden-Wurttemberg, Germany)
ISSN: 2198-3844
Titre abrégé: Adv Sci (Weinh)
Pays: Germany
ID NLM: 101664569

Informations de publication

Date de publication:
15 Feb 2024
Historique:
revised: 31 01 2024
received: 13 09 2023
medline: 15 2 2024
pubmed: 15 2 2024
entrez: 15 2 2024
Statut: aheadofprint

Résumé

Weibel Palade bodies (WPB) are lysosome-related secretory organelles of endothelial cells. Commonly known for their main cargo, the platelet and leukocyte receptors von-Willebrand factor (VWF) and P-selectin, WPB play a crucial role in hemostasis and inflammation. Here, the authors identify the glycerophosphodiester phosphodiesterase domain-containing protein 5 (GDPD5) as a WPB cargo protein and show that GDPD5 is transported to WPB following uptake from the plasma membrane via an unique endocytic transport route. GDPD5 cleaves GPI-anchored, plasma membrane-resident proteins within their GPI-motif, thereby regulating their local activity. The authors identify a novel target of GDPD5 , the complement regulator CD59, and show that it is released from the endothelial surface by GDPD5 following WPB exocytosis. This results in increased deposition of complement components and can enhance local inflammatory and thrombogenic responses. Thus, stimulus-induced WPB exocytosis can modify the endothelial cell surface by GDPD5-mediated selective release of a subset of GPI-anchored proteins.

Identifiants

pubmed: 38359017
doi: 10.1002/advs.202306624
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2306624

Subventions

Organisme : German Research Council
ID : DFG GE 514/6-3
Organisme : German Research Council
ID : SFB 1348
Organisme : Deutsche Forschungsgemeinschaft
ID : GE514/6-3VG),SFB1348(VG)

Informations de copyright

© 2024 The Authors. Advanced Science published by Wiley-VCH GmbH.

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Auteurs

Johannes Naß (J)

Institute of Medical Biochemistry, Center for Molecular Biology of Inflammation, University of Muenster, von-Esmarch-Str. 56, 48149, Muenster, Germany.

Julian Terglane (J)

Institute of Medical Biochemistry, Center for Molecular Biology of Inflammation, University of Muenster, von-Esmarch-Str. 56, 48149, Muenster, Germany.

Dagmar Zeuschner (D)

Electron Microscopy Facility, Max Planck Institute for Molecular Biomedicine, Roentgenstr. 20, 48149, Muenster, Germany.

Volker Gerke (V)

Institute of Medical Biochemistry, Center for Molecular Biology of Inflammation, University of Muenster, von-Esmarch-Str. 56, 48149, Muenster, Germany.

Classifications MeSH