Coronary Neutrophil Extracellular Trap Burden and Deoxyribonuclease Activity in ST-Elevation Acute Coronary Syndrome Are Predictors of ST-Segment Resolution and Infarct Size. Issue 7 (27th March 2015)
- Record Type:
- Journal Article
- Title:
- Coronary Neutrophil Extracellular Trap Burden and Deoxyribonuclease Activity in ST-Elevation Acute Coronary Syndrome Are Predictors of ST-Segment Resolution and Infarct Size. Issue 7 (27th March 2015)
- Main Title:
- Coronary Neutrophil Extracellular Trap Burden and Deoxyribonuclease Activity in ST-Elevation Acute Coronary Syndrome Are Predictors of ST-Segment Resolution and Infarct Size
- Authors:
- Mangold, Andreas
Alias, Sherin
Scherz, Thomas
Hofbauer, Thomas
Jakowitsch, Johannes
Panzenböck, Adelheid
Simon, Daniel
Laimer, Daniela
Bangert, Christine
Kammerlander, Andreas
Mascherbauer, Julia
Winter, Max-Paul
Distelmaier, Klaus
Adlbrecht, Christopher
Preissner, Klaus T.
Lang, Irene M. - Abstract:
- <abstract> <title> <x xml:space="preserve">Abstract</x> </title> <sec> <title> <underline>Rationale:</underline> </title> <p>Mechanisms of coronary occlusion in ST-elevation acute coronary syndrome are poorly understood. We have previously reported that neutrophil (polymorphonuclear cells [PMNs]) accumulation in culprit lesion site (CLS) thrombus is a predictor of cardiovascular outcomes.</p> </sec> <sec> <title> <underline>Objective:</underline> </title> <p>The goal of this study was to characterize PMN activation at the CLS. We examined the relationships between CLS neutrophil extracellular traps (NETs), bacterial components as triggers of NETosis, activity of endogenous deoxyribonuclease, ST-segment resolution, and infarct size.</p> </sec> <sec> <title> <underline>Methods and Results:</underline> </title> <p>We analyzed coronary thrombectomies from 111 patients with ST-elevation acute coronary syndrome undergoing primary percutaneous coronary intervention. Thrombi were characterized by immunostaining, flow cytometry, bacterial profiling, and immunometric and enzymatic assays. Compared with femoral PMNs, CLS PMNs were highly activated and formed aggregates with platelets. Nucleosomes, double-stranded DNA, neutrophil elastase, myeloperoxidase, and myeloid-related protein 8/14 were increased in CLS plasma, and NETs contributed to the scaffolds of particulate coronary thrombi. Copy numbers of Streptococcus species correlated positively with dsDNA. Thrombus NET burden<abstract> <title> <x xml:space="preserve">Abstract</x> </title> <sec> <title> <underline>Rationale:</underline> </title> <p>Mechanisms of coronary occlusion in ST-elevation acute coronary syndrome are poorly understood. We have previously reported that neutrophil (polymorphonuclear cells [PMNs]) accumulation in culprit lesion site (CLS) thrombus is a predictor of cardiovascular outcomes.</p> </sec> <sec> <title> <underline>Objective:</underline> </title> <p>The goal of this study was to characterize PMN activation at the CLS. We examined the relationships between CLS neutrophil extracellular traps (NETs), bacterial components as triggers of NETosis, activity of endogenous deoxyribonuclease, ST-segment resolution, and infarct size.</p> </sec> <sec> <title> <underline>Methods and Results:</underline> </title> <p>We analyzed coronary thrombectomies from 111 patients with ST-elevation acute coronary syndrome undergoing primary percutaneous coronary intervention. Thrombi were characterized by immunostaining, flow cytometry, bacterial profiling, and immunometric and enzymatic assays. Compared with femoral PMNs, CLS PMNs were highly activated and formed aggregates with platelets. Nucleosomes, double-stranded DNA, neutrophil elastase, myeloperoxidase, and myeloid-related protein 8/14 were increased in CLS plasma, and NETs contributed to the scaffolds of particulate coronary thrombi. Copy numbers of Streptococcus species correlated positively with dsDNA. Thrombus NET burden correlated positively with infarct size and negatively with ST-segment resolution, whereas CLS deoxyribonuclease activity correlated negatively with infarct size and positively with ST-segment resolution. Recombinant deoxyribonuclease accelerated the lysis of coronary thrombi ex vivo.</p> </sec> <sec> <title> <underline>Conclusions:</underline> </title> <p>PMNs are highly activated in ST-elevation acute coronary syndrome and undergo NETosis at the CLS. Coronary NET burden and deoxyribonuclease activity are predictors of ST-segment resolution and myocardial infarct size.</p> </sec> </abstract> … (more)
- Is Part Of:
- Circulation research. Volume 116:Issue 7(2015)
- Journal:
- Circulation research
- Issue:
- Volume 116:Issue 7(2015)
- Issue Display:
- Volume 116, Issue 7 (2015)
- Year:
- 2015
- Volume:
- 116
- Issue:
- 7
- Issue Sort Value:
- 2015-0116-0007-0000
- Page Start:
- Page End:
- Publication Date:
- 2015-03-27
- Subjects:
- Cardiovascular system -- Periodicals
Blood -- Circulation -- Periodicals
Blood Circulation
Cardiovascular System
Vascular Diseases
Sang -- Circulation -- Périodiques
Appareil cardiovasculaire -- Périodiques
612.1 - Journal URLs:
- http://circres.ahajournals.org/ ↗
http://www.circresaha.org ↗
http://journals.lww.com ↗ - DOI:
- 10.1161/CIRCRESAHA.116.304944 ↗
- Languages:
- English
- ISSNs:
- 0009-7330
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3265.300000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3607.xml