Factor XII, also known as Hageman factor, is a plasma protein and zymogen that plays a role in coagulation. It is encoded by the F12 gene and has a structure consisting of two fibronectin-type domains, two epidermal growth factor-like domains, a kringle domain, and a proline-rich region. Factor XII functions to initiate the intrinsic pathway of coagulation by being activated via contact with polyanions like polyphosphates secreted by activated platelets, linking primary hemostasis involving platelet plug formation to secondary hemostasis involving fibrin meshwork formation.
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2. Coagulation factor XII, also known as Hageman factor, is a plasma protein. It
is the zymogen form of factor XIIa, an enzyme (EC3.4.21.38) of the serine
protease (or serine endopeptidase) class. In humans, factor XII is encoded by
by the F12 gene.[5]
3. STRUCTURE
Human Factor XII is 596 amino acids long and consists of two domains,
Its heavy chain contains two fibronectin-type domains (type I and II),
two epidermal growth factor-like domains, a kringle domain, and a proline-
rich region
4. FUNCTION
factor XII is activated by contact to polyanions. Activated platelets secrete
inorganic polymers, polyphosphates. Contact to polyphosphates activates
factor XII and initiates fibrin formation by the intrinsic pathway of
coagulation with critical importance for thrombus formation.
5. Targeting polyphosphates with phosphatases interfered with procoagulant
activity of activated platelets and blocked platelet-induced thrombosis in
mice. Addition of polyphosphates restored defective plasma clotting
of HermanskyPudlak syndromepatients, indicating that the inorganic
polymer is the endogenous factor XII activator in vivo. Platelet
polyphosphate-driven factor XII activation provides the link from primary
hemostasis (formation of a platelet plug) to secondary hemostasis (fibrin
meshwork formation).[9]