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Air Bubbles Activate Complement and Trigger Hemostasis and C3-Dependent Cytokine Release Ex Vivo in Human Whole Blood

Venous air embolism, which may complicate medical and surgical procedures, activates complement and triggers thromboinflammation. In lepirudin-anticoagulated human whole blood, we examined the effect of air bubbles on complement and its role in thromboinflammation. Whole blood from 16 donors was inc...

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Autores principales: Storm, Benjamin S., Christiansen, Dorte, Fure, Hilde, Ludviksen, Judith K., Lau, Corinna, Lambris, John D., Woodruff, Trent M., Brekke, Ole-Lars, Braaten, Tonje, Nielsen, Erik W., Mollnes, Tom Eirik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AAI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8611197/
https://www.ncbi.nlm.nih.gov/pubmed/34732467
http://dx.doi.org/10.4049/jimmunol.2100308
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author Storm, Benjamin S.
Christiansen, Dorte
Fure, Hilde
Ludviksen, Judith K.
Lau, Corinna
Lambris, John D.
Woodruff, Trent M.
Brekke, Ole-Lars
Braaten, Tonje
Nielsen, Erik W.
Mollnes, Tom Eirik
author_facet Storm, Benjamin S.
Christiansen, Dorte
Fure, Hilde
Ludviksen, Judith K.
Lau, Corinna
Lambris, John D.
Woodruff, Trent M.
Brekke, Ole-Lars
Braaten, Tonje
Nielsen, Erik W.
Mollnes, Tom Eirik
author_sort Storm, Benjamin S.
collection PubMed
description Venous air embolism, which may complicate medical and surgical procedures, activates complement and triggers thromboinflammation. In lepirudin-anticoagulated human whole blood, we examined the effect of air bubbles on complement and its role in thromboinflammation. Whole blood from 16 donors was incubated with air bubbles without or with inhibitors of C3, C5, C5aR1, or CD14. Complement activation, hemostasis, and cytokine release were measured using ELISA and quantitative PCR. Compared with no air, incubating blood with air bubbles increased, on average, C3a 6.5-fold, C3bc 6-fold, C3bBbP 3.7-fold, C5a 4.6-fold, terminal complement complex sC5b9 3.6-fold, prothrombin fragments 1+2 (PTF1+2) 25-fold, tissue factor mRNA (TF-mRNA) 26-fold, microparticle tissue factor 6.1-fold, β-thromboglobulin 26-fold (all p < 0.05), and 25 cytokines 11-fold (range, 1.5–78-fold; all p < 0.0001). C3 inhibition attenuated complement and reduced PTF1+2 2-fold, TF-mRNA 5.4-fold, microparticle tissue factor 2-fold, and the 25 cytokines 2.7-fold (range, 1.4–4.9-fold; all p < 0.05). C5 inhibition reduced PTF1+2 2-fold and TF-mRNA 12-fold (all p < 0.05). C5 or CD14 inhibition alone reduced three cytokines, including IL-1β (p = 0.02 and p = 0.03). Combined C3 and CD14 inhibition reduced all cytokines 3.9-fold (range, 1.3–9.5-fold; p < 0.003) and was most pronounced for IL-1β (3.2- versus 6.4-fold), IL-6 (2.5- versus 9.3-fold), IL-8 (4.9- versus 8.6-fold), and IFN-γ (5- versus 9.5-fold). Antifoam activated complement and was avoided. PTF1+2 was generated in whole blood but not in plasma. In summary, air bubbles activated complement and triggered a C3-driven thromboinflammation. C3 inhibition reduced all mediators, whereas C5 inhibition reduced only TF-mRNA. Combined C5 and CD14 inhibition reduced IL-1β release. These data have implications for future mechanistic studies and possible pharmacological interventions in patients with air embolism.
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spelling pubmed-86111972021-12-01 Air Bubbles Activate Complement and Trigger Hemostasis and C3-Dependent Cytokine Release Ex Vivo in Human Whole Blood Storm, Benjamin S. Christiansen, Dorte Fure, Hilde Ludviksen, Judith K. Lau, Corinna Lambris, John D. Woodruff, Trent M. Brekke, Ole-Lars Braaten, Tonje Nielsen, Erik W. Mollnes, Tom Eirik J Immunol Innate Immunity and Inflammation Venous air embolism, which may complicate medical and surgical procedures, activates complement and triggers thromboinflammation. In lepirudin-anticoagulated human whole blood, we examined the effect of air bubbles on complement and its role in thromboinflammation. Whole blood from 16 donors was incubated with air bubbles without or with inhibitors of C3, C5, C5aR1, or CD14. Complement activation, hemostasis, and cytokine release were measured using ELISA and quantitative PCR. Compared with no air, incubating blood with air bubbles increased, on average, C3a 6.5-fold, C3bc 6-fold, C3bBbP 3.7-fold, C5a 4.6-fold, terminal complement complex sC5b9 3.6-fold, prothrombin fragments 1+2 (PTF1+2) 25-fold, tissue factor mRNA (TF-mRNA) 26-fold, microparticle tissue factor 6.1-fold, β-thromboglobulin 26-fold (all p < 0.05), and 25 cytokines 11-fold (range, 1.5–78-fold; all p < 0.0001). C3 inhibition attenuated complement and reduced PTF1+2 2-fold, TF-mRNA 5.4-fold, microparticle tissue factor 2-fold, and the 25 cytokines 2.7-fold (range, 1.4–4.9-fold; all p < 0.05). C5 inhibition reduced PTF1+2 2-fold and TF-mRNA 12-fold (all p < 0.05). C5 or CD14 inhibition alone reduced three cytokines, including IL-1β (p = 0.02 and p = 0.03). Combined C3 and CD14 inhibition reduced all cytokines 3.9-fold (range, 1.3–9.5-fold; p < 0.003) and was most pronounced for IL-1β (3.2- versus 6.4-fold), IL-6 (2.5- versus 9.3-fold), IL-8 (4.9- versus 8.6-fold), and IFN-γ (5- versus 9.5-fold). Antifoam activated complement and was avoided. PTF1+2 was generated in whole blood but not in plasma. In summary, air bubbles activated complement and triggered a C3-driven thromboinflammation. C3 inhibition reduced all mediators, whereas C5 inhibition reduced only TF-mRNA. Combined C5 and CD14 inhibition reduced IL-1β release. These data have implications for future mechanistic studies and possible pharmacological interventions in patients with air embolism. AAI 2021-12-01 2021-12-01 /pmc/articles/PMC8611197/ /pubmed/34732467 http://dx.doi.org/10.4049/jimmunol.2100308 Text en Copyright © 2021 by The Authors https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the CC BY 4.0 Unported license.
spellingShingle Innate Immunity and Inflammation
Storm, Benjamin S.
Christiansen, Dorte
Fure, Hilde
Ludviksen, Judith K.
Lau, Corinna
Lambris, John D.
Woodruff, Trent M.
Brekke, Ole-Lars
Braaten, Tonje
Nielsen, Erik W.
Mollnes, Tom Eirik
Air Bubbles Activate Complement and Trigger Hemostasis and C3-Dependent Cytokine Release Ex Vivo in Human Whole Blood
title Air Bubbles Activate Complement and Trigger Hemostasis and C3-Dependent Cytokine Release Ex Vivo in Human Whole Blood
title_full Air Bubbles Activate Complement and Trigger Hemostasis and C3-Dependent Cytokine Release Ex Vivo in Human Whole Blood
title_fullStr Air Bubbles Activate Complement and Trigger Hemostasis and C3-Dependent Cytokine Release Ex Vivo in Human Whole Blood
title_full_unstemmed Air Bubbles Activate Complement and Trigger Hemostasis and C3-Dependent Cytokine Release Ex Vivo in Human Whole Blood
title_short Air Bubbles Activate Complement and Trigger Hemostasis and C3-Dependent Cytokine Release Ex Vivo in Human Whole Blood
title_sort air bubbles activate complement and trigger hemostasis and c3-dependent cytokine release ex vivo in human whole blood
topic Innate Immunity and Inflammation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8611197/
https://www.ncbi.nlm.nih.gov/pubmed/34732467
http://dx.doi.org/10.4049/jimmunol.2100308
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