FSAP reduces risk of repair

Overenthusiastic repair of damaged blood vessels could cause a fatal blockage. Sedding et al. (page 2801) report that the normal repair-restricting function of factor VII activating protease (FSAP) is disrupted by a common mutation. People carrying the mutation might thus be more at risk of vessel narrowing.

Approximately 5% of the population carries an FSAP polymorphism linked to cardiovascular disease. The authors' previous in vitro evidence suggested that wild-type FSAP, a plasma protein, limits vessel repair processes in part by inactivating PDGF-BB—a growth factor which promotes the proliferation and migration of blood vessel wall cells during repair.

The team isolated and characterized the mutated form of FSAP and discovered that although its ability to bind PDGF-BB was unaltered, it failed to cleave the protein efficiently....