Tr. De Wit et Ja. Van Mourik, Biosynthesis, processing and secretion of von Willebrand factor: biological implications, BEST P R C, 14(2), 2001, pp. 241-255
von Willebrand factor is a multimeric plasma glycoprotein that is required
for normal haemostasis. von Willebrand factor is synthesized by endothelial
cells and megakaryocytes, and originates from its precursor pro-von Willeb
rand factor. The endoproteolytic processing of pro-von Willebrand factor re
sults in mature von Willebrand factor and von Willebrand factor propeptide
(also known as von Willebrand Ag II). In endothelial cells, the propeptide
controls the polymerization and subsequent targeting of von Willebrand fact
or to the storage vesicles, the so-called Weibel-Palade bodies. Upon stimul
ation of the endothelial cells, the Weibel-Palade bod ies are translocated
to the plasma membrane of the cell, and mature von Willebrand factor and it
s propeptide are co-secreted. After release, these polypeptides have diverg
ent fates and serve different biological functions. Mature von Willebrand f
actor both controls platelet adhesion and aggregation at sites of vascular
injury and acts as a chaperone protein for coagulation factor VIII. The von
Willebrand factor propeptide may serve a role in modulating inflammatory p
rocesses. This still growing body of information indicates that the biologi
cal function of the von Willebrand factor gene product is more diverse than
was previously thought.