Key result
Shear-activated platelets release 21 specific lipids at higher levels than biochemical stimulation, uniquely altering the lipidome.
Why the study?
Little is known regarding platelet lipid alterations occurring with mechanical, shear-mediated platelet activation, an important driver of thrombotic risk in implantable blood-contacting devices for heart failure.
Does shear-mediated platelet activation induce unique lipidome changes compared to biochemical activation in human platelets?
Does shear-mediated platelet activation induce unique lipidome changes compared to biochemical activation in human platelets?
Shear-mediated platelet activation induces unique lipidomic alterations compared to biochemical activation, which may contribute to thrombosis in patients with implanted cardiovascular devices.
Answers are grounded in this paper and cite their sources.
Shear-specific platelet lipid release may promote device thrombosis; leaves open targeted lipid modulation in mechanical circulatory support.
Platelet activation by mechanical means such as shear stress, is a vital driver of thrombotic risk in implantable blood-contacting devices used in treatment of heart failure. Lipids are essential in platelets activation and have been studied following biochemical activation. However, little is known regarding lipid alterations occurring with mechanical – shear mediated platelet activation. Here, we determined if shear-activation of platelets induced lipidome changes that differ from those associated with biochemically-mediated platelet activation. We performed high-resolution lipidomic analysis on purified platelets from four healthy human donors. For each donor, we compared the lipidome of platelets that were non-activated or activated by shear, ADP, or thrombin treatment. We found that shear activation altered cell-associated lipids and led to the release of lipids into the extracellular environment. Shear-activated platelets released 21 phospholipids and sphingomyelins at levels statistically higher than platelets activated by biochemical stimulation. Many of the released phospholipids contained an arachidonic acid tail or were phosphatidylserine lipids, which have procoagulant properties. We conclude that shear-mediated activation of platelets alters the basal platelet lipidome. Further, these alterations differ and are unique in comparison to the lipidome of biochemically activated platelets. Our findings suggest that lipids released by shear-activated platelets may contribute to altered thrombosis in patients with implanted cardiovascular therapeutic devices.
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Sweedo et al. (2021) studied Healthy (n=4). Shear-mediated platelet activation vs. Non-activated, ADP, or thrombin treatment was evaluated on Lipidome changes. Shear-activated platelets released 21 phospholipids and sphingomyelins at statistically higher levels than biochemically stimulated platelets, uniquely altering the basal platelet lipidome.
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