Search bioRxiv⌕ Search

Biology subjects

Shepeliuk, T. O.

Publications and source records attributed to Shepeliuk, T. O..

2 recordsLinked to original sources

Burst-like Secretion of Platelet Dense Granules Promotes Thrombus Shell Expansion

Vessel-wall injury triggers platelet recruitment and aggregation with exquisite spatiotemporal regulation. While secreted agonists from thrombin-activated platelets play a crucial role in thrombus formation, the underlying mechanisms remain elusive. Using real-time imaging of isolated human platelets, we demonstrate that dense granules, which are enriched with agonists, are released in brief, stochastic bursts driven by intracellular calcium spikes, which are necessary but not individually sufficient to trigger secretion events. This burst-like secretion is sustained through extracellular feedback, establishing a cooperative, probabilistic mechanism of granule release in which released agonists amplify thrombin-induced granule exocytosis and increase the likelihood of secretion bursts. Computational modeling of whole-thrombus growth reveals that these transient bursts generate localized microdomains of high agonist concentration, facilitating expansion of the outer thrombus layers. Our findings establish burst-like secretion as a distinct hemostatic mechanism that enhances platelet recruitment and orchestrates thrombus architecture through localized, self-reinforcing activation. Key pointsO_LILive imaging reveals dense granules secretion in discrete bursts. C_LIO_LIIntracellular calcium spikes are necessary but not sufficient for triggering secretion events. C_LIO_LIBurst-like secretion arises from cooperativity, driven by the feedback amplification from the extracellularly released granule content. C_LIO_LIBurst-like dense granule secretion promotes dynamic expansion of the thrombus shell in silico. C_LI

cell biology↗

Hidden Complexity of Pediatric Platelet Disorders: Functional Diversity and Unexpected Hypercoagulable Phenotypes

Pediatric platelet disorders are commonly classified according to specific structural or functional abnormalities, yet it remains unclear how well these diagnoses capture overall hemostatic phenotype. Here, we combined quantitative single-cell platelet measurements with spatially resolved plasma clotting analysis to characterize pediatric patients with dense granule deficiency, platelet function defects, immune thrombocytopenia, and other inherited platelet disorders. Quantitative fluorescence microscopy revealed reduced dense granule abundance not only in dense granule deficiency but also in several patients from other diagnostic groups. Measurements of platelet adhesion, spreading, and calcium signaling identified substantial functional diversity, with individual patients exhibiting distinct combinations of abnormalities that were not predicted by diagnostic category. Unexpectedly, plasma clotting analysis frequently revealed hypercoagulable behavior, including accelerated fibrin clot growth and spontaneous fibrin formation, despite clinical diagnoses associated with platelet-related bleeding disorders. Hypercoagulable phenotypes occurred across multiple diagnostic groups and did not show a simple relationship with platelet functional abnormalities. Together, these findings reveal previously unrecognized complexity in pediatric platelet disorders and suggest that platelet and plasma pathways contribute independently to hemostatic variability. These findings argue that pediatric platelet disorders are best viewed as multidimensional functional phenotypes rather than isolated platelet defects and motivate broader integration of platelet and coagulation measurements in future studies.

cell biology↗