Mazurier C, Goudemand J
Laboratoire de recherche sur l'hémostase, Lille.
Rev Prat. 1997 Dec 15;47(20):2233-8.
Normal endothelium, as well as megakaryocytes, produces and secretes von Willebrand factor which plays a pivotal role in haemostasis. It mediates platelet adhesion and shear-stress-induced aggregation at the site of vessel wall injury and also serves as a carrier protein of factor VIII, an essential cofactor in coagulation. The quantitative or qualitative abnormalities of von Willebrand factor lead to von Willebrand disease, the most common congenital bleeding disorder. Over the past few years major progress in the knowledge of the synthesis, structure and functions of von Willebrand factor have led to improve the diagnosis and treatment of the different molecular forms of von Willebrand disease.
正常内皮细胞以及巨核细胞都会产生并分泌血管性血友病因子,该因子在止血过程中起关键作用。它介导血小板在血管壁损伤部位的黏附以及剪切应力诱导的聚集,并且还作为凝血因子VIII的载体蛋白,而凝血因子VIII是凝血过程中必不可少的辅助因子。血管性血友病因子的定量或定性异常会导致血管性血友病,这是最常见的先天性出血性疾病。在过去几年中,对血管性血友病因子的合成、结构和功能的认识取得了重大进展,从而改善了对不同分子形式血管性血友病的诊断和治疗。