Semin Thromb Hemost 2018; 44(02): 176-184
DOI: 10.1055/s-0037-1604092
Review Article
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Vitamin K–Dependent Protein S: Beyond the Protein C Pathway

Björn Dahlbäck
Department of Translational Medicine, Lund University, Malmö, Sweden
› Author Affiliations
Further Information

Publication History

Publication Date:
13 September 2017 (eFirst)


Protein S is a vitamin K–dependent plasma glycoprotein circulating in plasma at a concentration of around 350 nM. Approximately 60% of protein S in human plasma is bound to the complement regulatory protein C4b-binding protein (C4BP) in a high-affinity, high-molecular-weight complex. Protein S in plasma has multiple anticoagulant properties and heterozygous protein S deficiency is associated with increased risk of venous thrombosis. Homozygous deficiency in man and mice is associated with severe thrombosis in fetal life, defects in the vascular system development, and not compatible with life. Protein S has additional functions beyond being an anticoagulant. It affects the complement regulatory properties of C4BP, and moreover, protein S interacts with tyrosine kinase receptors of the TAM family, which comprises Tyro3, Axl, and Mer. The TAM receptor interaction is important for the ability of protein S to stimulate phagocytosis of apoptotic cells. This review will discuss the multiple functions of protein S, describing its role as cofactor to activated protein C with a subsequent focus on the other functions of protein S.