Search: (WFRF:(Hansen John Bjarne)) >
Sustained and inter...
-
Wahlund, Casper J.E.Thrombosis Research Group (TREC), Department of Clinical Medicine, UiT, The Arctic University of Norway, Tromsø, Norway
(author)
Sustained and intermittent hypoxia differentially modulate primary monocyte immunothrombotic responses to IL-1β stimulation
- Article/chapterEnglish2023
Publisher, publication year, extent ...
-
Frontiers Media SA,2023
-
printrdacarrier
Numbers
-
LIBRIS-ID:oai:DiVA.org:kth-337415
-
https://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-337415URI
-
https://doi.org/10.3389/fimmu.2023.1240597DOI
-
https://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-223227URI
Supplementary language notes
-
Language:English
-
Summary in:English
Part of subdatabase
Classification
-
Subject category:ref swepub-contenttype
-
Subject category:art swepub-publicationtype
Notes
-
QC 20231003
-
Venous thromboembolism (VTE) is a leading cause of preventable deaths in hospitals, and its incidence is not decreasing despite extensive efforts in clinical and laboratory research. Venous thrombi are primarily formed in the valve pockets of deep veins, where activated monocytes play a crucial role in bridging innate immune activation and hemostatic pathways through the production of inflammatory cytokines, chemokines, and tissue factor (TF) – a principal initiator of coagulation. In the valve pocket inflammation and hypoxia (sustained/intermittent) coexist, however their combined effects on immunothrombotic processes are poorly understood. Inflammation is strongly associated with VTE, while the additional contribution of hypoxia remains largely unexplored. To investigate this, we modelled the intricate conditions of the venous valve pocket using a state-of-the-art hypoxia chamber with software-controlled oxygen cycling. We comprehensively studied the effects of sustained and intermittent hypoxia alone, and in combination with VTE-associated inflammatory stimuli on primary monocytes. TF expression and activity was measured in monocytes subjected to sustained and intermittent hypoxia alone, or in combination with IL-1β. Monocyte responses were further analyzed in detailed by RNA sequencing and validated by ELISA. Stimulation with IL-1β alone promoted both transcription and activity of TF. Interestingly, the stimulatory effect of IL-1β on TF was attenuated by sustained hypoxia, but not by intermittent hypoxia. Our transcriptome analysis further confirmed that sustained hypoxia limited the pro-inflammatory response induced by IL-1β, and triggered a metabolic shift in monocytes. Intermittent hypoxia alone had a modest effect on monocyte transcript. However, in combination with IL-1β intermittent hypoxia significantly altered the expression of 2207 genes and enhanced the IL-1β-stimulatory effects on several chemokine and interleukin genes (e.g., IL-19, IL-24, IL-32, MIF), as well as genes involved in coagulation (thrombomodulin) and fibrinolysis (VEGFA, MMP9, MMP14 and PAI-1). Increased production of CCL2, IL-6 and TNF following stimulation with intermittent hypoxia and IL-1β was confirmed by ELISA. Our findings provide valuable insights into how the different hypoxic profiles shape the immunothrombotic response of monocytes and shed new light on the early events in the pathogenesis of venous thrombosis.
Subject headings and genre
Added entries (persons, corporate bodies, meetings, titles ...)
-
Çaglayan, SafakThrombosis Research Group (TREC), Department of Clinical Medicine, UiT, The Arctic University of Norway, Tromsø, Norway
(author)
-
Czarnewski, PauloStockholms universitet,KTH,Science for Life Laboratory, SciLifeLab,Genteknologi,Department of Biochemistry and Biophysics, National Bioinformatics Infrastructure Sweden, Stockholm University, Stockholm, Sweden,Institutionen för biokemi och biofysik,Science for Life Laboratory (SciLifeLab),Science for Life Laboratory, Department of Gene Technology, KTH Royal Institute of Technology, Stockholm, Sweden(Swepub:su)pacz1456
(author)
-
Hansen, John BjarneThrombosis Research Group (TREC), Department of Clinical Medicine, UiT, The Arctic University of Norway, Tromsø, Norway; Division of Internal Medicine, University Hospital of North Norway, Tromsø, Norway
(author)
-
Snir, OmriThrombosis Research Group (TREC), Department of Clinical Medicine, UiT, The Arctic University of Norway, Tromsø, Norway; Division of Internal Medicine, University Hospital of North Norway, Tromsø, Norway
(author)
-
Thrombosis Research Group (TREC), Department of Clinical Medicine, UiT, The Arctic University of Norway, Tromsø, NorwayScience for Life Laboratory, SciLifeLab
(creator_code:org_t)
Related titles
-
In:Frontiers in Immunology: Frontiers Media SA141664-3224
Internet link
Find in a library
To the university's database