Neutrophil Extracellular Traps may be a Potential Target for Treating Early Brain Injury in Subarachnoid Hemorrhage
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- 14 April 2021
- journal article
- research article
- Published by Springer Nature in Translational Stroke Research
- Vol. 13 (1) , 112-131
Abstract
Neuroinflammation is closely associated with poor prognosis in patients with subarachnoid hemorrhage (SAH). The purpose of this study was to investigate the role of neutrophil extracellular traps (NETs), which are important regulators of sterile inflammation, in SAH. In this study, markers of NET formation, quantified by the level of citrullinated histone H3 (CitH3), were significantly increased after SAH and correlated with SAH severity. CitH3 peaked at 12 h in peripheral blood and at 24 h in the brain. Administration of the peptidyl arginine deiminase 4 (PAD4) selective antagonist GSK484 substantially attenuated SAH-induced brain edema and neuronal injury. Moreover, the benefit of NET inhibition was also confirmed by DNAse I treatment and neutrophil depletion. Mechanistically, NETs markedly exacerbated microglial inflammation in vitro. NET formation aggravated neuroinflammation by promoting microglial activation and increased the levels of TNF-α, IL-1β, and IL-6, while inhibiting NETs demonstrated anti-inflammatory effects by decreasing the levels of these proinflammatory factors. Moreover, neurogenic pulmonary edema (NPE), a severe nonneurological complication after SAH, is associated with a high level of NET formation. However, GSK484 effectively inhibited the formation of NETs in the lungs of NPE mice, thereby preventing the diffusion of neutrophilic infiltration and attenuating the swelling of the alveolar interstitium. In conclusion, NETs promoted neuroinflammation after SAH, while pharmacological inhibition of PAD4-NETs could reduce the inflammatory damage caused by SAH. These results supported the idea that NETs might be potential therapeutic targets for SAH.Keywords
Funding Information
- National Key R&D Program of China (2018YFC1312600, 2018YFC1312603)
- Key Research and Development Project of Zhejiang Province (no.2018C03011)
- National Natural Science Foundation of China (no.81771246, 81971099, 81870908, 81901234, 81601003, 81801144, 81701152)
This publication has 58 references indexed in Scilit:
- Early Brain Injury: A Common Mechanism in Subarachnoid Hemorrhage and Global Cerebral IschemiaStroke Research and Treatment, 2013
- Neutrophil Extracellular Traps: Double-Edged Swords of Innate ImmunityThe Journal of Immunology, 2012
- Neutrophil Cerebrovascular Transmigration Triggers Rapid Neurotoxicity through Release of Proteases Associated with Decondensed DNAThe Journal of Immunology, 2012
- Guidelines for the Management of Aneurysmal Subarachnoid HemorrhageStroke, 2012
- Sterile inflammation: sensing and reacting to damageNature Reviews Immunology, 2010
- Caspase-1 Inhibitor Prevents Neurogenic Pulmonary Edema After Subarachnoid Hemorrhage in MiceStroke, 2009
- Chapter 25 Oxidative Stress in Stroke Pathophysiology2009
- MMP-9–Positive Neutrophil Infiltration Is Associated to Blood–Brain Barrier Breakdown and Basal Lamina Type IV Collagen Degradation During Hemorrhagic Transformation After Human Ischemic StrokeStroke, 2008
- Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT MethodMethods, 2001
- Pulmonary edema following fatal aneurysm ruptureJournal of Neurosurgery, 1978