Clotting factors

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Clotting factors are proteins that circulate in plasma in an inactive state. Their main function is to enable hemocoagulation (blood clotting). Most of them are produced by the liver.

Factor Name

Alternative name

Function
I fibrinogen cleavage of several peptides produces monomeric fibrin, which further forms a fibrin network
II* prothrombin its active form (IIa) activates factors I, V, VII, VIII, XI, XIII, protein C and platelets
III tissue thromboplastin

tissue factor

factor VIIa cofactor
IV Ca2+ binding of coagulation factors to phospholipids
V proaccelerin, labile factor, accelerating globulin factor X cofactor – ensure the conversion of prothrombin into active thrombin
VI older name for factor Va
VII* proconvertin activates factors IX, X
VIII antihemophilic factor (AHF)

antihemophilic factor A - antihemophilic globulin (AHG)

factor IX cofactor
IX* The Christmas factor

plasma thromboplastin component (PTC) - antihemophilic factor B

activates factor X
X* Stuart-Prower factor** activates factor II
XI plasma precursor of thromboplastin

plasma thromboplastin antecedent (PTA) - antihemophilic factor C

activates factor IX
XII The Hageman factor

glass factor

activates factor XI, VII and prekallikrein
XIII fibrin stabilizing factor

Laki-Lorand factor

von Willebrand factor binds to factor VIII, enables platelet adhesion
high molecular weight kininogen (HMWK) Fitzgerald Factor supports the mutual activation of XII, XI and prekallikrein
prekallikrein (PKK)

Fletcher factor

activates factor XII and prekallikrein, cleaves HMWK
kallikrein
platelet phospholipids

* vitamin K dependent

** named after the first two patients (Mr R. Stuart and Miss A. Prower) in whom factor X deficiency was described


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Bibliography[edit | edit source]

  • GANONG, William F. Přehled lékařské fyziologie. 20. edition. Galén, 2005. pp. 546–549. ISBN 80-7262-311-7.
  • KITTNAR, Otomar. Lékařská fyziologie. 1. edition. Grada, 2003. 790 pp. ISBN 978-80-247-3068-4.