124 research outputs found
āGoing with the flowā in modeling fibrinolysis
Funding CSW and NJM are supported by the British Heart Foundation (PG/20/17/35050) and a NC3Rs-British Heart Foundation Studentship (NC/W001810/1).Peer reviewedPublisher PD
uPA-mediated plasminogen activation is enhanced by polyphosphate
Funding This research was supported by grants FS/11/2/28579 (NJM) and PG/11/1/28461 (NJM, CSW) from the British Heart Foundation.Peer reviewedPublisher PD
Location, location, location : Fibrin, cells, and fibrinolytic factors in thrombi
Funding Information: Figures were created with BioRender.com.Peer reviewedPublisher PD
Factor XIII-A : An Indispensable āFactorā in Haemostasis and Wound Healing
Author Contributions: F.S.M.A. wrote the manuscript; C.S.W. supervised the research and wrote the manuscript; N.J.M. supervised the research and wrote the manuscript. All authors have read and agreed to the published version of the manuscript. Funding: Fahad S.M. Alshehri is supported by Royal Embassy of Saudi Arabia Cultural Bureau (KFMCS74). Claire S. Whyte and Nicola J. Mutch were supported by the British Heart Foundation project grants (PG/15/82/31721 and PG/20/17/35050). Acknowledgments: All figures were prepared with https://biorender.com/ (accessed on 16 March 2021).Peer reviewedPublisher PD
A serpin with a finger in many PAIās : PAI-1ās central function in thromboinflammation and cardiovascular disease
FUNDING NM and CW are funded by grants from the British Heart Foundation PG/15/82/31721 and PG/20/17/35050 and Friends of Anchor RS 2019 003 and Aberdeen Development Trust. GM, CW, and NM were also funded by NHS Grampian Endowment Fund COV19-004.Peer reviewedPublisher PD
The Efficacy of Fibrinogen Concentrates in Relation to Cryoprecipitate in Restoring Clot Integrity and Stability against Lysis
Funding: This work was supported in part by Tenovus Scotland Grampian (G17.03) and Friends of Anchor (SC025332). C.S.W. and N.J.M. were supported by the British Heart Foundation (PG/15/82/31721and PG/20/17/35050). Acknowledgments: We thank the NHS Grampian Haematology department for kindly performing the Clauss assay to measure the fibrinogen concentration in the cryoprecipitate. We thank the University of Aberdeen Microscopy and Histology facility for their advice and the use of their facilities. We thank Linda Robertson and Megan Simpson for their technical assistance.Peer reviewedPublisher PD
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Fibrinolytic abnormalities in acute respiratory distress syndrome (ARDS) and versatility of thrombolytic drugs to treat COVIDā19
The global pandemic of coronavirus disease 2019 (COVIDā19) is associated with the development of acute respiratory distress syndrome (ARDS), which requires ventilation in critically ill patients. The pathophysiology of ARDS results from acute inflammation within the alveolar space and prevention of normal gas exchange. The increase in proinflammatory cytokines within the lung leads to recruitment of leukocytes, further propagating the local inflammatory response. A consistent finding in ARDS is the deposition of fibrin in the air spaces and lung parenchyma. COVIDā19 patients show elevated Dādimers and fibrinogen. Fibrin deposits are found in the lungs of patients due to the dysregulation of the coagulation and fibrinolytic systems. Tissue factor (TF) is exposed on damaged alveolar endothelial cells and on the surface of leukocytes promoting fibrin deposition, while significantly elevated levels of plasminogen activator inhibitor 1 (PAIā1) from lung epithelium and endothelial cells create a hypofibrinolytic state. Prophylaxis treatment of COVIDā19 patients with low molecular weight heparin (LMWH) is important to limit coagulopathy. However, to degrade preāexisting fibrin in the lung it is essential to promote local fibrinolysis. In this review, we discuss the repurposing of fibrinolytic drugs, namely tissueātype plasminogen activator (tPA), to treat COVIDā19 associated ARDS. tPA is an approved intravenous thrombolytic treatment, and the nebulizer form has been shown to be effective in plastic bronchitis and is currently in Phase II clinical trial. Nebulizer plasminogen activators may provide a targeted approach in COVIDā19 patients to degrade fibrin and improving oxygenation in critically ill patients
Location, location, location: Fibrin, cells, and fibrinolytic factors in thrombi
Thrombi are heterogenous in nature with composition and structure being dictated by the site of formation, initiating stimuli, shear stress, and cellular influences. Arterial thrombi are historically associated with high platelet content and more tightly packed fibrin, reflecting the shear stress in these vessels. In contrast, venous thrombi are generally erythrocyte and fibrin-rich with reduced platelet contribution. However, these conventional views on the composition of thrombi in divergent vascular beds have shifted in recent years, largely due to recent advances in thromboectomy and high-resolution imaging. Interestingly, the distribution of fibrinolytic proteins within thrombi is directly influenced by the cellular composition and vascular bed. This in turn influences the susceptibility of thrombi to proteolytic degradation. Our current knowledge of thrombus composition and its impact on resistance to thrombolytic therapy and success of thrombectomy is advancing, but nonetheless in its infancy. We require a deeper understanding of thrombus architecture and the downstream influence on fibrinolytic susceptibility. Ultimately, this will aid in a stratified and targeted approach to tailored antithrombotic strategies in patients with various thromboembolic diseases
āSuperā SERPINsāA stabilizing force against fibrinolysis in thromboinflammatory conditions
The superfamily of serine protease inhibitors (SERPINs) are a class of inhibitors that utilise a dynamic conformational change to trap and inhibit their target enzymes. Their powerful nature lends itself well to regulation of complex physiological enzymatic cascades, such as the haemostatic, inflammatory and complement pathways. The SERPINs Ī±2-antiplasmin, plasminogen-activator inhibitor-1, plasminogen-activator inhibitor-2, protease nexin-1, and C1-inhibitor play crucial inhibitory roles in regulation of the fibrinolytic system and inflammation. Elevated levels of these SERPINs are associated with increased risk of thrombotic complications, obesity, type 2 diabetes, and hypertension. Conversely, deficiencies of these SERPINs have been linked to hyperfibrinolysis with bleeding and angioedema. In recent years SERPINs have been implicated in the modulation of the immune response and various thromboinflammatory conditions, such as sepsis and COVID-19. Here, we highlight the current understanding of the physiological role of SERPINs in haemostasis and inflammatory disease progression, with emphasis on the fibrinolytic pathway, and how this becomes dysregulated during disease. Finally, we consider the role of these SERPINs as potential biomarkers of disease progression and therapeutic targets for thromboinflammatory diseases
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