Year: 2015
Type: article
Abstract: BACKGROUND: Platelets are central to the process of hemostasis, rapidly aggregating at sites of blood vessel injury and acting as coagulation nidus sites. On interaction with the subendothelial matrix, platelets are transformed into balloonlike structures as part of the hemostatic response. It remains unclear, however, how and why platelets generate these structures. We set out to determine the physiological relevance and cellular and molecular mechanisms underlying platelet membrane ballooning. METHODS AND RESULTS: Using 4-dimensional live-cell imaging and electron microscopy, we show that human platelets adherent to collagen are transformed into phosphatidylserine-exposing balloonlike structures with expansive macro/microvesiculate contact surfaces, by a process that we termed procoagulant spreading. We reveal that ballooning is mechanistically and structurally distinct from membrane blebbing and involves disruption to the platelet microtubule cytoskeleton and inflation through fluid entry. Unlike blebbing, procoagulant ballooning is irreversible and a consequence of Na(+), Cl(-), and water entry. Furthermore, membrane ballooning correlated with microparticle generation. Inhibition of Na(+), Cl(-), or water entry impaired ballooning, procoagulant spreading, and microparticle generation, and it also diminished local thrombin generation. Human Scott syndrome platelets, which lack expression of Ano-6, also showed a marked reduction in membrane ballooning, consistent with a role for chloride entry in the process. Finally, the blockade of water entry by acetazolamide attenuated ballooning in vitro and markedly suppressed thrombus formation in vivo in a mouse model of thrombosis. CONCLUSIONS: Ballooning and procoagulant spreading of platelets are driven by fluid entry into the cells, and are important for the amplification of localized coagulation in thrombosis.
Source: Circulation
Language: English
Subfield: Hematology
Field: Medicine
Domain: Health Sciences
Open Access status: bronze
Awards: Role of the two-pore channel TPCN1 in regulating platelet calcium signalling, function and thrombosis, Role of the motor protein myosin Va in regulating platelet secretion and function, Contribution of the PI(3,4,5)P3 binding adaptor protein Bam32 to PI3 kinase- mediated platelet function and arterial thrombosis, G4426845423, G5299442232, G5707489769, G5942728609, Investigations into the role of insulin/ IGF receptor heterodimers in platelet function, Development of a novel clinical platelet analyser, G7223224048, RENEWAL: Protein kinase C-dependent platelet secretion: central regulator of thrombosis and atherogenesis, Investigations into the role of the PI(3,4,5) P3 binding protein Rasa3 in platelet function and thrombosis, Role of sharpin in platelet integrin αIIbβ3 and α2β1regulation and thrombus formation
OpenAlex ID: W2158792289
