Polyphosphate Activates von Willebrand Factor Interaction with Glycoprotein Ib in the Absence of Factor VIII In Vitro

Polyphosphate (polyP), a phosphate polymer released by activated platelets, may modulate various stages of hemostasis by binding to blood proteins. In this context, we previously reported that polyP binds to the von Willebrand factor (VWF). One of the most significant functions of VWF is to bind to...

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Autores:
Montilla Rodríguez, Liliana Marcela
Atienza- Navarro, Isabel
García- Cozar, Francisco Jose
Castro, Carmen
Rodriguez- Martorell, Francisco Javier
Ruiz, Felix A
Tipo de recurso:
Article of investigation
Fecha de publicación:
2022
Institución:
Universidad Cooperativa de Colombia
Repositorio:
Repositorio UCC
Idioma:
OAI Identifier:
oai:repository.ucc.edu.co:20.500.12494/52561
Acceso en línea:
https://doi.org/10.3390/ijms232214118
https://hdl.handle.net/20.500.12494/52561
Palabra clave:
Factor VIII
Hemophilia A
Polyphosphate
Von Willebrand disease
Von Willebrand factor
Rights
openAccess
License
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