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Murine thrombus organization limits access to high platelet activation states while supporting platelet recruitment

  • Sung W. Rhee
  • , Irina D. Pokrovskaya
  • , Kelly K. Ball
  • , Michael W. Webb
  • , Jeffrey A. Kamykowski
  • , Maria A. Aronova
  • , Richard D. Leapman
  • , Elizabeth R. Driehaus
  • , Erich S. Franz
  • , Sidney W. Whiteheart
  • , Brian Storrie

Producción científica: Articlerevisión exhaustiva

Resumen

Platelet aggregation at sites of vascular injury is essential for hemostasis. However, the mechanisms that prevent excessive clot growth are not fully understood. In the prevailing “core and shell” model, based largely on small vessel injury studies, a central core of highly activated platelets is surrounded by a limited signal intensity shell of less activated, minimally degranulated platelets. Recent reports, especially in mouse models of profuse bleeding, suggest thrombus architecture and platelet activation states are more heterogeneous than the binary core and shell model proposes. Here, we performed high-resolution morphometric mapping of individual platelet activation states in mouse jugular vein and femoral artery puncture wound thrombi, using serial block face scanning electron microscopy and wide-area transmission electron microscopy. Manually annotated images were analyzed at multiple time points, revealing initial, 1-minute, near-complete intermixing of platelet activation states with no distinct core of highly activated platelets. At 5 minutes, highly activated, degranulated platelets became concentrated along the interior surfaces of vaulted thrombus structures. At 20 minutes, platelet numbers decreased and distinct clustering of degranulated, highly activated platelets was observed within central portions of the intravascular platelet-rich crown, limiting their access to the circulation. Deletion of the α-granule vesicle-soluble N-ethylmaleimide-sensitive factor attachment protein receptor, vesicle associated membrane protein 8, increased both the frequency and clustering of highly activated platelets. Similar patterns were observed in femoral artery wounds. We conclude that thrombus organization is more complex than previously recognized and provide evidence that progressive structural changes help limit procoagulant surface exposure and thrombus growth during hemostasis after puncture wounding.

Idioma originalEnglish
Número de artículo100154
PublicaciónBlood Vessels, Thrombosis and Hemostasis
Volumen3
N.º2
DOI
EstadoPublished - may 2026

Nota bibliográfica

Publisher Copyright:
© 2026 The American Society of Hematology

Financiación

Work at all sites was supported by the National Heart, Lung, and Blood Institute of the National Institutes of Health (NIH): University of Arkansas for Medical Sciences (NIH grants R01 HL119393, R56 HL119393, and R01 155519 [B.S.]) and subawards from NIH grants R01 HL146373 and R35 HL150818; University of Pennsylvania (NIH grants P01 HL040387 [Timothy J. Stalker]) and P01 HL120846 ([Timothy J. Stalker and Lawrence F. Brass]); University of Kentucky (NIH grant MIRA HL150818 [S.W.W.]). The Leapman laboratory was supported by the intramural program of the National Institute of Biomedical Imaging and Bioengineering at the NIH .

FinanciadoresNúmero del financiador
National Institute of Biomedical Imaging and Bioengineering
National Institutes of Health (NIH)
National Heart, Lung, and Blood Institute (NHLBI)
University of Arkansas for Medical SciencesR56 HL119393, R01 155519, R35 HL150818, R01 HL119393, R01 HL146373
The Pennsylvania State UniversityP01 HL040387, P01 HL120846
University of KentuckyMIRA HL150818

    ASJC Scopus subject areas

    • Surgery
    • Hematology
    • Oncology
    • Cardiology and Cardiovascular Medicine

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