Recombinant Thrombomodulin Suppresses Histone-Induced Neutrophil Extracellular Trap Formation

Bibliographic Details
Title: Recombinant Thrombomodulin Suppresses Histone-Induced Neutrophil Extracellular Trap Formation
Authors: Binita Shrestha, Takashi Ito, Midori Kakuuchi, Takaaki Totoki, Tomoka Nagasato, Mika Yamamoto, Ikuro Maruyama
Source: Frontiers in Immunology, Vol 10 (2019)
Publisher Information: Frontiers Media S.A., 2019.
Publication Year: 2019
Collection: LCC:Immunologic diseases. Allergy
Subject Terms: histone, NETs, thrombomodulin, thrombosis, neutrophil, Immunologic diseases. Allergy, RC581-607
More Details: Histones, the major protein components of chromatin, are released into the extracellular space during sepsis, trauma, and ischemia-reperfusion injury, and subsequently mediate organ failure. Extracellular histones can promote endothelial damage and platelet aggregation, which can be suppressed by administration of recombinant thrombomodulin (rTM). The present study aimed to clarify whether histones can activate neutrophils to induce NET formation and whether rTM can prevent histone-induced NET formation. NET formation was analyzed in vitro by stimulating human neutrophils with histones in the absence or presence of rTM. NET formation was further analyzed in vivo by intravenous infusion of histones into rats with or without rTM. Histones induced NET release in a dose-dependent manner in vitro and NET release was induced as early as 1 h after stimulation. Histone-induced NET release was independent of NADPH oxidase. rTM suppressed histone-induced NET release in vitro as well as in vivo. The suppression might be mediated by rTM binding to histones, as suggested by analysis using a quartz crystal microbalance system. The present findings suggest that histones can activate neutrophils to form NETs and that rTM can inhibit histone-induced NET formation.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1664-3224
Relation: https://www.frontiersin.org/article/10.3389/fimmu.2019.02535/full; https://doaj.org/toc/1664-3224
DOI: 10.3389/fimmu.2019.02535
Access URL: https://doaj.org/article/5158d3f6370f4301b3cb259c1dc5583e
Accession Number: edsdoj.5158d3f6370f4301b3cb259c1dc5583e
Database: Directory of Open Access Journals
More Details
ISSN:16643224
DOI:10.3389/fimmu.2019.02535
Published in:Frontiers in Immunology
Language:English