Zheng, Ruiyuan ORCID: 0000-0002-7594-3869, Moynahan, Kyle, Georgomanolis, Theodoros ORCID: 0000-0002-4066-9257, Pavlenko, Egor ORCID: 0000-0003-0293-052X, Geissen, Simon ORCID: 0000-0002-7835-4111, Mizi, Athanasia, Grimm, Simon ORCID: 0000-0002-0786-2207, Nemade, Harshal ORCID: 0000-0002-2704-181X, Rehimi, Rizwan, Bastigkeit, Jil ORCID: 0000-0001-9148-4044, Lackmann, Jan-Wilm ORCID: 0000-0001-8182-8034, Adam, Matti ORCID: 0000-0002-6990-8135, Rada-Iglesias, Alvaro, Nuernberg, Peter ORCID: 0009-0009-8276-7910, Klinke, Anna, Poepsel, Simon ORCID: 0000-0002-8304-4062, Baldus, Stephan ORCID: 0000-0001-8259-1737, Papantonis, Argyris and Kargapolova, Yulia ORCID: 0000-0001-7541-5778 (2024). Remodeling of the endothelial cell transcriptional program via paracrine and DNA-binding activities of MPO. iScience, 27 (2). pp. 1-20. Elsevier. ISSN 2589-0042

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Identification Number:10.1016/j.isci.2024.108898

Abstract

[Artikel-Nr.: 108898] Myeloperoxidase (MPO) is an enzyme that functions in host defense. MPO is released into the vascular lumen by neutrophils during inflammation and may adhere and subsequently penetrate endothelial cells (ECs) coating vascular walls. We show that MPO enters the nucleus of ECs and binds chromatin independently of its enzymatic activity. MPO drives chromatin decondensation at its binding sites and enhances condensation at neighboring regions. It binds loci relevant for endothelial-to-mesenchymal transition (EndMT) and affects the migratory potential of ECs. Finally, MPO interacts with the RNA-binding factor ILF3 thereby affecting its relative abundance between cytoplasm and nucleus. This interaction leads to change in stability of ILF3-bound transcripts. MPO-knockout mice exhibit reduced number of ECs at scar sites following myocardial infarction, indicating reduced neovascularization. In summary, we describe a non-enzymatic role for MPO in coordinating EndMT and controlling the fate of endothelial cells through direct chromatin binding and association with co-factors.

Item Type: Article
Creators:
Creators
Email
ORCID
ORCID Put Code
Zheng, Ruiyuan
UNSPECIFIED
UNSPECIFIED
Moynahan, Kyle
UNSPECIFIED
UNSPECIFIED
UNSPECIFIED
Georgomanolis, Theodoros
UNSPECIFIED
UNSPECIFIED
Pavlenko, Egor
UNSPECIFIED
UNSPECIFIED
Geissen, Simon
UNSPECIFIED
UNSPECIFIED
Mizi, Athanasia
UNSPECIFIED
UNSPECIFIED
UNSPECIFIED
Grimm, Simon
UNSPECIFIED
UNSPECIFIED
Nemade, Harshal
UNSPECIFIED
UNSPECIFIED
Rehimi, Rizwan
UNSPECIFIED
UNSPECIFIED
UNSPECIFIED
Bastigkeit, Jil
UNSPECIFIED
UNSPECIFIED
Lackmann, Jan-Wilm
UNSPECIFIED
UNSPECIFIED
Adam, Matti
UNSPECIFIED
UNSPECIFIED
Rada-Iglesias, Alvaro
UNSPECIFIED
UNSPECIFIED
UNSPECIFIED
Nuernberg, Peter
UNSPECIFIED
UNSPECIFIED
Klinke, Anna
UNSPECIFIED
UNSPECIFIED
UNSPECIFIED
Poepsel, Simon
UNSPECIFIED
UNSPECIFIED
Baldus, Stephan
UNSPECIFIED
UNSPECIFIED
Papantonis, Argyris
UNSPECIFIED
UNSPECIFIED
UNSPECIFIED
Kargapolova, Yulia
UNSPECIFIED
UNSPECIFIED
URN: urn:nbn:de:hbz:38-814008
Identification Number: 10.1016/j.isci.2024.108898
Journal or Publication Title: iScience
Volume: 27
Number: 2
Page Range: pp. 1-20
Number of Pages: 20
Date: 16 February 2024
Publisher: Elsevier
ISSN: 2589-0042
Language: English
Faculty: Faculty of Medicine
Divisions: CECAD - Cluster of Excellence Cellular Stress Responses in Aging-Associated Diseases
Cologne Center for Genomics
Faculty of Medicine > Innere Medizin > Klinik III für Innere Medizin - Kardiologie, Pneumologie, Angiologie und internistische Intensivmedizin
Zentrum für Molekulare Medizin
Subjects: Life sciences
Medical sciences Medicine
['eprint_fieldname_oa_funders' not defined]: Publikationsfonds UzK
Refereed: Yes
URI: http://kups.ub.uni-koeln.de/id/eprint/81400

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