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Heparin Forms Polymers with Cell-free DNA Which Elongate Under Shear in Flowing Blood
Heparin is a widely used anticoagulant which inhibits factor Xa and thrombin through potentiation of antithrombin. We recently identified that the nucleic acid stain SYTOX reacts with platelet polyphosphate due to molecular similarities, some of which are shared by heparin. We attempted to study hep...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6892814/ https://www.ncbi.nlm.nih.gov/pubmed/31797980 http://dx.doi.org/10.1038/s41598-019-54818-3 |
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author | de Vries, Joost C. Barendrecht, Arjan D. Clark, Chantal C. Urbanus, Rolf T. Boross, Peter de Maat, Steven Maas, Coen |
author_facet | de Vries, Joost C. Barendrecht, Arjan D. Clark, Chantal C. Urbanus, Rolf T. Boross, Peter de Maat, Steven Maas, Coen |
author_sort | de Vries, Joost C. |
collection | PubMed |
description | Heparin is a widely used anticoagulant which inhibits factor Xa and thrombin through potentiation of antithrombin. We recently identified that the nucleic acid stain SYTOX reacts with platelet polyphosphate due to molecular similarities, some of which are shared by heparin. We attempted to study heparin in flowing blood by live-cell fluorescence microscopy, using SYTOX for heparin visualisation. Immunostaining was performed with monoclonal antibodies directed against various heparin-binding proteins. In addition, we studied modulation of heparin activity in coagulation assays, as well its effects on fibrin formation under flow in recalcified whole blood. We found that SYTOX-positive polymers appear in heparinised blood under flow. These polymers typically associate with platelet aggregates and their length (reversibly) increases with shear rate. Immunostaining revealed that of the heparin-binding proteins assessed, they only contain histones. In coagulation assays and flow studies on fibrin formation, we found that addition of exogenous histones reverses the anticoagulant effects of heparin. Furthermore, the polymers do not appear in the presence of DNase I, heparinase I/III, or the heparin antidote protamine. These findings suggest that heparin forms polymeric complexes with cell-free DNA in whole blood through a currently unidentified mechanism. |
format | Online Article Text |
id | pubmed-6892814 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68928142019-12-10 Heparin Forms Polymers with Cell-free DNA Which Elongate Under Shear in Flowing Blood de Vries, Joost C. Barendrecht, Arjan D. Clark, Chantal C. Urbanus, Rolf T. Boross, Peter de Maat, Steven Maas, Coen Sci Rep Article Heparin is a widely used anticoagulant which inhibits factor Xa and thrombin through potentiation of antithrombin. We recently identified that the nucleic acid stain SYTOX reacts with platelet polyphosphate due to molecular similarities, some of which are shared by heparin. We attempted to study heparin in flowing blood by live-cell fluorescence microscopy, using SYTOX for heparin visualisation. Immunostaining was performed with monoclonal antibodies directed against various heparin-binding proteins. In addition, we studied modulation of heparin activity in coagulation assays, as well its effects on fibrin formation under flow in recalcified whole blood. We found that SYTOX-positive polymers appear in heparinised blood under flow. These polymers typically associate with platelet aggregates and their length (reversibly) increases with shear rate. Immunostaining revealed that of the heparin-binding proteins assessed, they only contain histones. In coagulation assays and flow studies on fibrin formation, we found that addition of exogenous histones reverses the anticoagulant effects of heparin. Furthermore, the polymers do not appear in the presence of DNase I, heparinase I/III, or the heparin antidote protamine. These findings suggest that heparin forms polymeric complexes with cell-free DNA in whole blood through a currently unidentified mechanism. Nature Publishing Group UK 2019-12-04 /pmc/articles/PMC6892814/ /pubmed/31797980 http://dx.doi.org/10.1038/s41598-019-54818-3 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article de Vries, Joost C. Barendrecht, Arjan D. Clark, Chantal C. Urbanus, Rolf T. Boross, Peter de Maat, Steven Maas, Coen Heparin Forms Polymers with Cell-free DNA Which Elongate Under Shear in Flowing Blood |
title | Heparin Forms Polymers with Cell-free DNA Which Elongate Under Shear in Flowing Blood |
title_full | Heparin Forms Polymers with Cell-free DNA Which Elongate Under Shear in Flowing Blood |
title_fullStr | Heparin Forms Polymers with Cell-free DNA Which Elongate Under Shear in Flowing Blood |
title_full_unstemmed | Heparin Forms Polymers with Cell-free DNA Which Elongate Under Shear in Flowing Blood |
title_short | Heparin Forms Polymers with Cell-free DNA Which Elongate Under Shear in Flowing Blood |
title_sort | heparin forms polymers with cell-free dna which elongate under shear in flowing blood |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6892814/ https://www.ncbi.nlm.nih.gov/pubmed/31797980 http://dx.doi.org/10.1038/s41598-019-54818-3 |
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