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Effects of Diabetes Mellitus on Fibrin Clot Structure and Mechanics in a Model of Acute Neutrophil Extracellular Traps (NETs) Formation
Subjects with diabetes mellitus (DM) have an increased risk of arterial thrombosis, to which changes in clot structure and mechanics may contribute. Another contributing factor might be an increased formation of neutrophil extracellular traps (NETs) in DM. NETs are mainly formed during the acute pha...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7582521/ https://www.ncbi.nlm.nih.gov/pubmed/32993159 http://dx.doi.org/10.3390/ijms21197107 |
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author | de Vries, Judith J. Hoppenbrouwers, Tamara Martinez-Torres, Cristina Majied, Rezin Özcan, Behiye van Hoek, Mandy Leebeek, Frank W.G. Rijken, Dingeman C. Koenderink, Gijsje H. de Maat, Moniek P.M. |
author_facet | de Vries, Judith J. Hoppenbrouwers, Tamara Martinez-Torres, Cristina Majied, Rezin Özcan, Behiye van Hoek, Mandy Leebeek, Frank W.G. Rijken, Dingeman C. Koenderink, Gijsje H. de Maat, Moniek P.M. |
author_sort | de Vries, Judith J. |
collection | PubMed |
description | Subjects with diabetes mellitus (DM) have an increased risk of arterial thrombosis, to which changes in clot structure and mechanics may contribute. Another contributing factor might be an increased formation of neutrophil extracellular traps (NETs) in DM. NETs are mainly formed during the acute phase of disease and form a network within the fibrin matrix, thereby influencing clot properties. Previous research has shown separate effects of NETs and DM on clot properties, therefore our aim was to study how DM affects clot properties in a model resembling an acute phase of disease with NETs formation. Clots were prepared from citrated plasma from subjects with and without DM with the addition of NETs, induced in neutrophils by S. aureus bacteria or phorbol myristate acetate (PMA). Structural parameters were measured using scanning electron microscopy, mechanical properties using rheology, and sensitivity to lysis using a fluorescence-based fibrinolysis assay. Plasma clots from subjects with DM had significantly thicker fibers and fewer pores and branch points than clots from subjects without DM. In addition, fibrinolysis was significantly slower, while mechanical properties were similar between both groups. In conclusion, in a model of acute NETs formation, DM plasma shows prothrombotic effects on fibrin clots. |
format | Online Article Text |
id | pubmed-7582521 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-75825212020-10-29 Effects of Diabetes Mellitus on Fibrin Clot Structure and Mechanics in a Model of Acute Neutrophil Extracellular Traps (NETs) Formation de Vries, Judith J. Hoppenbrouwers, Tamara Martinez-Torres, Cristina Majied, Rezin Özcan, Behiye van Hoek, Mandy Leebeek, Frank W.G. Rijken, Dingeman C. Koenderink, Gijsje H. de Maat, Moniek P.M. Int J Mol Sci Article Subjects with diabetes mellitus (DM) have an increased risk of arterial thrombosis, to which changes in clot structure and mechanics may contribute. Another contributing factor might be an increased formation of neutrophil extracellular traps (NETs) in DM. NETs are mainly formed during the acute phase of disease and form a network within the fibrin matrix, thereby influencing clot properties. Previous research has shown separate effects of NETs and DM on clot properties, therefore our aim was to study how DM affects clot properties in a model resembling an acute phase of disease with NETs formation. Clots were prepared from citrated plasma from subjects with and without DM with the addition of NETs, induced in neutrophils by S. aureus bacteria or phorbol myristate acetate (PMA). Structural parameters were measured using scanning electron microscopy, mechanical properties using rheology, and sensitivity to lysis using a fluorescence-based fibrinolysis assay. Plasma clots from subjects with DM had significantly thicker fibers and fewer pores and branch points than clots from subjects without DM. In addition, fibrinolysis was significantly slower, while mechanical properties were similar between both groups. In conclusion, in a model of acute NETs formation, DM plasma shows prothrombotic effects on fibrin clots. MDPI 2020-09-26 /pmc/articles/PMC7582521/ /pubmed/32993159 http://dx.doi.org/10.3390/ijms21197107 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article de Vries, Judith J. Hoppenbrouwers, Tamara Martinez-Torres, Cristina Majied, Rezin Özcan, Behiye van Hoek, Mandy Leebeek, Frank W.G. Rijken, Dingeman C. Koenderink, Gijsje H. de Maat, Moniek P.M. Effects of Diabetes Mellitus on Fibrin Clot Structure and Mechanics in a Model of Acute Neutrophil Extracellular Traps (NETs) Formation |
title | Effects of Diabetes Mellitus on Fibrin Clot Structure and Mechanics in a Model of Acute Neutrophil Extracellular Traps (NETs) Formation |
title_full | Effects of Diabetes Mellitus on Fibrin Clot Structure and Mechanics in a Model of Acute Neutrophil Extracellular Traps (NETs) Formation |
title_fullStr | Effects of Diabetes Mellitus on Fibrin Clot Structure and Mechanics in a Model of Acute Neutrophil Extracellular Traps (NETs) Formation |
title_full_unstemmed | Effects of Diabetes Mellitus on Fibrin Clot Structure and Mechanics in a Model of Acute Neutrophil Extracellular Traps (NETs) Formation |
title_short | Effects of Diabetes Mellitus on Fibrin Clot Structure and Mechanics in a Model of Acute Neutrophil Extracellular Traps (NETs) Formation |
title_sort | effects of diabetes mellitus on fibrin clot structure and mechanics in a model of acute neutrophil extracellular traps (nets) formation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7582521/ https://www.ncbi.nlm.nih.gov/pubmed/32993159 http://dx.doi.org/10.3390/ijms21197107 |
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