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Fatal dysfunction and disintegration of thrombin-stimulated platelets

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dc.contributor.author Kim O.
dc.contributor.author Nevzorova T.
dc.contributor.author Mordakhanova E.
dc.contributor.author Ponomareva A.
dc.contributor.author Andrianova I.
dc.contributor.author Minh G.
dc.contributor.author Daminova A.
dc.contributor.author Peshkova A.
dc.contributor.author Alber M.
dc.contributor.author Vagin O.
dc.contributor.author Litvinov R.
dc.contributor.author Weisel J.
dc.date.accessioned 2020-01-15T21:18:43Z
dc.date.available 2020-01-15T21:18:43Z
dc.date.issued 2019
dc.identifier.issn 0390-6078
dc.identifier.uri https://dspace.kpfu.ru/xmlui/handle/net/155644
dc.description.abstract © 2019 Ferrata Storti Foundation. Platelets play a key role in the formation of hemostatic clots and obstructive thrombi as well as in other biological processes. In response to physiological stimulants, including thrombin, platelets change shape, express adhesive molecules, aggregate, and secrete bioactive substances, but their subsequent fate is largely unknown. Here we examined late-stage structural, metabolic, and functional consequences of thrombin- induced platelet activation. Using a combination of confocal microscopy, scanning and transmission electron microscopy, flow cytometry, biochemical and biomechanical measurements, we showed that thrombin- induced activation is followed by time-dependent platelet dysfunction and disintegration. After ~30 minutes of incubation with thrombin, unlike with collagen or ADP, human platelets disintegrated into cellular fragments containing organelles, such as mitochondria, glycogen granules, and vacuoles. This platelet fragmentation was preceded by Ca2+ influx, integrin aIIbâ3 activation and phosphatidylserine exposure (activation phase), followed by mitochondrial depolarization, generation of reactive oxygen species, metabolic ATP depletion and impairment of platelet contractility along with dramatic cytoskeletal rearrangements, concomitant with platelet disintegration (death phase). Coincidentally with the platelet fragmentation, thrombin caused calpain activation but not activation of caspases 3 and 7. Our findings indicate that the late functional and structural damage of thrombin-activated platelets comprise a calpain-dependent platelet death pathway that shares some similarities with the programmed death of nucleated cells, but is unique to platelets, therefore representing a special form of cellular destruction. Fragmentation of activated platelets suggests that there is an underappreciated pathway of enhanced elimination of platelets from the circulation in (pro)thrombotic conditions once these cells have performed their functions.
dc.relation.ispartofseries Haematologica
dc.title Fatal dysfunction and disintegration of thrombin-stimulated platelets
dc.type Article
dc.relation.ispartofseries-issue 9
dc.relation.ispartofseries-volume 104
dc.collection Публикации сотрудников КФУ
dc.relation.startpage 1866
dc.source.id SCOPUS03906078-2019-104-9-SID85066922086


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  • Публикации сотрудников КФУ Scopus [24551]
    Коллекция содержит публикации сотрудников Казанского федерального (до 2010 года Казанского государственного) университета, проиндексированные в БД Scopus, начиная с 1970г.

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