Endogenous THBD (Thrombomodulin) Mediates Angiogenesis in the Ischemic Brain-Brief Report.


Journal

Arteriosclerosis, thrombosis, and vascular biology
ISSN: 1524-4636
Titre abrégé: Arterioscler Thromb Vasc Biol
Pays: United States
ID NLM: 9505803

Informations de publication

Date de publication:
12 2020
Historique:
pubmed: 9 10 2020
medline: 15 12 2020
entrez: 8 10 2020
Statut: ppublish

Résumé

THBD (thrombomodulin) is part of the anticoagulant protein C-system that acts at the endothelium and is involved in anti-inflammatory and barrier-stabilizing processes. A recombinant soluble form of THBD was shown to have protective effects in different organs, but how the endogenous THBD is regulated during ischemia, particularly in the brain is not known to date. The aim of this study was to investigate the role of THBD, especially in brain endothelial cells, during ischemic stroke. Approach and Results: To induce ischemic brain damage, we occluded the middle cerebral artery of mice. We found an increased endothelial expression of Endogenous THBD acts as a protective factor in the brain during ischemic stroke and enhances vessel diameter and proliferation. These previously unknown properties of THBD could offer new opportunities to affect vessel function after ischemia and thereby improve stroke outcome.

Identifiants

pubmed: 33028093
doi: 10.1161/ATVBAHA.120.315061
doi:

Substances chimiques

THBD protein, mouse 0
Thrombomodulin 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

2837-2844

Commentaires et corrections

Type : CommentIn

Auteurs

Jan Wenzel (J)

Institute for Experimental and Clinical Pharmacology and Toxicology, Center of Brain, Behavior and Metabolism (CBBM), University of Lübeck, Germany (J.W., D.S., J.C.A., M.A.K., I.S., B.L., S.K., M.S.).
German Centre for Cardiovascular Research (DZHK), partner site Hamburg/Kiel/Lübeck, Germany (J.W., D.S., M.S.).

Dimitrios Spyropoulos (D)

Institute for Experimental and Clinical Pharmacology and Toxicology, Center of Brain, Behavior and Metabolism (CBBM), University of Lübeck, Germany (J.W., D.S., J.C.A., M.A.K., I.S., B.L., S.K., M.S.).
German Centre for Cardiovascular Research (DZHK), partner site Hamburg/Kiel/Lübeck, Germany (J.W., D.S., M.S.).

Julian Christopher Assmann (JC)

Institute for Experimental and Clinical Pharmacology and Toxicology, Center of Brain, Behavior and Metabolism (CBBM), University of Lübeck, Germany (J.W., D.S., J.C.A., M.A.K., I.S., B.L., S.K., M.S.).

Mahtab Ahmad Khan (MA)

Institute for Experimental and Clinical Pharmacology and Toxicology, Center of Brain, Behavior and Metabolism (CBBM), University of Lübeck, Germany (J.W., D.S., J.C.A., M.A.K., I.S., B.L., S.K., M.S.).

Ines Stölting (I)

Institute for Experimental and Clinical Pharmacology and Toxicology, Center of Brain, Behavior and Metabolism (CBBM), University of Lübeck, Germany (J.W., D.S., J.C.A., M.A.K., I.S., B.L., S.K., M.S.).

Beate Lembrich (B)

Institute for Experimental and Clinical Pharmacology and Toxicology, Center of Brain, Behavior and Metabolism (CBBM), University of Lübeck, Germany (J.W., D.S., J.C.A., M.A.K., I.S., B.L., S.K., M.S.).

Sara Kreißig (S)

Institute for Experimental and Clinical Pharmacology and Toxicology, Center of Brain, Behavior and Metabolism (CBBM), University of Lübeck, Germany (J.W., D.S., J.C.A., M.A.K., I.S., B.L., S.K., M.S.).

Dirk Andreas Ridder (DA)

Institute of Pathology, Mainz University Medical Center, Germany (D.A.R.).

Berend Isermann (B)

Institute for Laboratory Medicine, Clinical Chemistry and Molecular Diagnostics, University of Leipzig, Germany (B.I.).

Markus Schwaninger (M)

Institute for Experimental and Clinical Pharmacology and Toxicology, Center of Brain, Behavior and Metabolism (CBBM), University of Lübeck, Germany (J.W., D.S., J.C.A., M.A.K., I.S., B.L., S.K., M.S.).
German Centre for Cardiovascular Research (DZHK), partner site Hamburg/Kiel/Lübeck, Germany (J.W., D.S., M.S.).

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Classifications MeSH