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dc.contributor.authorSweedo, Alice
dc.contributor.authorWise, Lisa M.
dc.contributor.authorRoka-Moiia, Yana
dc.contributor.authorArce, Fernando Teran
dc.contributor.authorSaavedra, S. Scott
dc.contributor.authorSheriff, Jawaad
dc.contributor.authorBluestein, Danny
dc.contributor.authorSlepian, Marvin J.
dc.contributor.authorPurdy, John G.
dc.date.accessioned2021-10-11T17:50:52Z
dc.date.available2021-10-11T17:50:52Z
dc.date.issued2021-08-25
dc.identifier.citationSweedo, A., Wise, L. M., Roka-Moiia, Y., Arce, F. T., Saavedra, S. S., Sheriff, J., Bluestein, D., Slepian, M. J., & Purdy, J. G. (2021). Shear-Mediated Platelet Activation is Accompanied by Unique Alterations in Platelet Release of Lipids. Cellular and Molecular Bioengineering.en_US
dc.identifier.issn1865-5025
dc.identifier.doi10.1007/s12195-021-00692-x
dc.identifier.urihttp://hdl.handle.net/10150/662068
dc.description.abstractIntroduction: Platelet activation by mechanical means such as shear stress exposure, is a vital driver of thrombotic risk in implantable blood-contacting devices used in the 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. Methods: 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. Results: 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. Conclusions: 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. Many of the released phospholipids contained an arachidonic acid tail or were phosphatidylserine lipids, which have known procoagulant properties. Our findings suggest that lipids released by shear-activated platelets may contribute to altered thrombosis in patients with implanted cardiovascular therapeutic devices. © 2021, Biomedical Engineering Society.en_US
dc.description.sponsorshipArizona Biomedical Research Commissionen_US
dc.language.isoenen_US
dc.publisherSpringer Science and Business Media LLCen_US
dc.rightsCopyright © 2021 Biomedical Engineering Society.en_US
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/en_US
dc.subjectCardiovascular diseaseen_US
dc.subjectLipidomicsen_US
dc.subjectMechanical circulatory supporten_US
dc.subjectMechanobiologyen_US
dc.subjectPlateletsen_US
dc.subjectShear activationen_US
dc.titleShear-Mediated Platelet Activation is Accompanied by Unique Alterations in Platelet Release of Lipidsen_US
dc.typeArticleen_US
dc.identifier.eissn1865-5033
dc.contributor.departmentDepartment of Biomedical Engineering, University of Arizonaen_US
dc.contributor.departmentDepartment of Immunobiology, University of Arizonaen_US
dc.contributor.departmentBIO5 Institute, University of Arizonaen_US
dc.contributor.departmentDepartment of Medicine, Sarver Heart Center, University of Arizonaen_US
dc.contributor.departmentDepartment of Chemistry and Biochemistry, University of Arizonaen_US
dc.contributor.departmentDepartment of Material Sciences and Engineering, University of Arizonaen_US
dc.identifier.journalCellular and Molecular Bioengineeringen_US
dc.description.note12 month embargo; published: 25 August 2021en_US
dc.description.collectioninformationThis item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.en_US
dc.eprint.versionFinal accepted manuscripten_US
dc.identifier.pii692
dc.source.journaltitleCellular and Molecular Bioengineering


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