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Individual variations in platelet reactivity towards ADP, epinephrine, collagen and nitric oxide, and the association to arterial function in young, healthy adults
Örebro University, School of Medical Sciences. (Cardiovascular Research Centre (CVRC))ORCID iD: 0000-0002-2732-158x
Örebro University, School of Medical Sciences. (Cardiovascular Research Centre (CVRC))ORCID iD: 0000-0002-6520-9265
Örebro University, School of Medical Sciences. (Cardiovascular Research Centre (CVRC))ORCID iD: 0000-0003-4253-3369
Örebro University, School of Medical Sciences. (Cardiovascular Research Centre (CVRC))ORCID iD: 0000-0003-2519-203X
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2019 (English)In: Thrombosis Research, ISSN 0049-3848, E-ISSN 1879-2472, Vol. 174, p. 5-12Article in journal (Refereed) Published
Abstract [en]

INTRODUCTION: Platelet aggregation and secretion can be induced by a large number of endogenous activators, such as collagen, adenosine diphosphate (ADP) and epinephrine. Conversely, the blood vessel endothelium constitutively release platelet inhibitors including nitric oxide (NO) and prostacyclin. NO and prostacyclin are also well-known vasodilators and contribute to alterations in local blood flow and systemic blood pressure.

MATERIALS AND METHODS: In this study we investigated individual variations in platelet reactivity and arterial functions including blood pressure and flow-mediated vasodilation (FMD) in 43 young, healthy individuals participating in the Lifestyle, Biomarkers and Atherosclerosis (LBA) study. Platelet aggregation and dense granule secretion were measured simultaneously by light transmission and luminescence. FMD was measured with ultrasound.

RESULTS: The platelet function assay showed inter-individual differences in platelet reactivity. Specifically, a sub-group of individuals had platelets with an increased response to low concentrations of ADP and epinephrine, but not collagen. When the NO-donor S-nitroso-N-acetyl-DL-penicillamine (SNAP) was combined with high doses of these platelet activators, the results indicated for sub-groups of NO-sensitive and NO-insensitive platelets. The individuals with NO-sensitive platelets in response to SNAP in combination with collagen had a higher capacity of FMD of the arteria brachialis.

CONCLUSIONS: Platelet reactivity towards ADP, epinephrine and NO differs between young, healthy individuals. Some individuals have a more effective response towards NO, both in the aspect of platelet inhibition ex vivo, as well as vasodilation in vivo.

Place, publisher, year, edition, pages
Elsevier, 2019. Vol. 174, p. 5-12
Keywords [en]
Adenosine diphosphate, Collagen, Epinephrine, Nitric oxide, Platelet activation, Vasodilation
National Category
Physiology Hematology Cardiac and Cardiovascular Systems
Identifiers
URN: urn:nbn:se:oru:diva-70787DOI: 10.1016/j.thromres.2018.12.008ISI: 000456949100002PubMedID: 30543988Scopus ID: 2-s2.0-85058021347OAI: oai:DiVA.org:oru-70787DiVA, id: diva2:1271996
Funder
AFA Insurance, 130275Knowledge FoundationAvailable from: 2018-12-18 Created: 2018-12-18 Last updated: 2024-03-06Bibliographically approved
In thesis
1. Impact of Interleukin-6 family cytokine signalling on human endothelial cells and platelets
Open this publication in new window or tab >>Impact of Interleukin-6 family cytokine signalling on human endothelial cells and platelets
2020 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Endothelial cells lining the luminal side of blood vessels creates a barrier between the circulating blood and the extracellular matrix. Endothelial cells have important functions in regulation of vessel tension and inflammation. Furthermore, endothelium-derived vasodilators prevent our smallest blood cells, platelets, to aggregate in the circulation. The main physiological role of platelets is to protect us from bleeding by creating aggregates at sites of injury. Platelets is also increasingly recognised as mediators in acute inflammation. The focus of this thesis has been to study the impact of inflammatory cytokines in the interleukin (IL)-6 family on endothelial cells and platelets. IL-6 has pleiotropic effects where IL-6 trans-signalling via the soluble IL-6 receptor (IL-6R) is associated to more pro-inflammatory outcomes than classic signalling via the membrane bound IL-6R. Both classic and trans-signalling need the ubiquitously expressed glycoprotein (gp)130 to induce intracellular signalling. Since the IL-6R is expressed on a restricted number of cell types, transsignalling exerts a broader IL-6 response. Paper I reveal that endothelial cells express IL-6R which facilitates both classic and trans-signalling. IL-6 trans-signalling activates more signalling pathways and results in proinflammatory responses in contrast to classic signalling. Paper II show that IL-6 trans-signalling, but not classic signalling occurs in platelets and results in inhibition of epinephrine-induced platelet aggregation. Paper III reveal inter-individual differences in platelet reactivity towards activators and the inhibitor nitric oxide (NO). Individuals with more NOsensitive platelets showed greater capacity of vasodilation, indicating a connection between endothelial function and platelet inhibition. In Paper IV, the impact of various gp130 signalling cytokines on endothelial cells revealed differences and similarities in intracellular signalling, gene expression and protein release. In summary, this thesis investigates the impact of the IL-6 family cytokines on endothelial cells and platelets in regards of intracellular signalling and functional responses.

Place, publisher, year, edition, pages
Örebro: Örebro University, 2020. p. 53
Series
Örebro Studies in Medicine, ISSN 1652-4063 ; 224
Keywords
gp130 signalling cytokines, inflammation, transsignalling, JAK/STAT, MEK/ERK, PI3K/AKT, platelet aggregation, vasodilation
National Category
Other Basic Medicine
Identifiers
urn:nbn:se:oru:diva-86353 (URN)978-91-7529-359-2 (ISBN)
Public defence
2020-12-03, Örebro universitet, Campus USÖ, hörsal C1, Södra Grev Rosengatan 32, Örebro, 13:00 (English)
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Supervisors
Available from: 2020-10-09 Created: 2020-10-09 Last updated: 2024-03-06Bibliographically approved

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Lindkvist, MadeleneFernberg, UlrikaLjungberg, LizaFälker, KnutFernström, MariaHurtig-Wennlöf, AnitaGrenegård, Magnus

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