Blood CoagulationFactors Involved in Blood CoagulationBlood Coagulation PathwayBlood Clotting Disorders
Blood Coagulation
Blood coagulation or clotting is an important phenomenon to prevent excess loss of blood in case of injury or trauma. The blood stops flowing from a wound in case of injury. The blood clot or βcoagulumβ is formed by a network of fibrin threads. In this network, deformed and dead formed elements (erythrocytes, leukocytes and platelets) get trapped.
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Prothrombin is the inactive form of thrombin that is present in the plasma. Thrombokinase converts prothrombin to active thrombin which in turn activates fibrinogen to fibrin. All these clotting factors help in blood coagulation.
An injury stimulates platelets or thrombocytes to release various factors that initiate the blood clotting cascade. Calcium ions play an important role in blood coagulation.
Letβs learn more in detail about the process of blood coagulation (clotting).
Factors Involved in Blood CoagulationΒ
First let’s glance at the coagulation factors involved in the blood clotting process.
Coagulation of blood occurs through a series of reactions due to the activation of a group of substances called clotting factors. There are 13 clotting factors identified and named after the scientists who discovered them or as per the activity. Only factor IX or Christmas factor is named after the patient in whom it was discovered.
Factor I FibrinogenΒ | Factor VI UnassignedΒ | Factor XI Plasma thromboplastin antecedent |
Factor II ProthrombinΒ | Factor VII Stable factorΒ | Factor XII Hageman factorΒ |
Factor III Thromboplastin | Factor VIII Antihemophilic factorΒ | Factor XIII Fibrin-stabilising factorΒ |
Factor IV Calcium Factor | Factor IX Christmas factor | |
Factor V Labile factor (Proaccelerin) | Factor X Stuart-Prower factor |
Blood Coagulation Pathway
The process of blood coagulation leads to haemostasis, i.e. prevention of bleeding or haemorrhage. Blood clotting involves activation and aggregation of platelets at the exposed endothelial cells, followed by deposition and stabilisation of cross-linked fibrin mesh.
Primary haemostasis involves platelet aggregation and formation of a plug at the site of injury, and secondary haemostasis involves strengthening and stabilisation of platelet plug by the formation of a network of fibrin threads. The secondary haemostasis involves two coagulation pathways, the intrinsic pathway and the extrinsic pathway. Both pathways merge at a point and lead to the activation of fibrin, and the formation of the fibrin network.
Platelet Activation
The blood circulating in the blood vessel does not clot under normal circumstances. The blood coagulation process is stimulated when there is any damage to the endothelium of blood vessels. It leads to platelet activation and aggregation. When collagen is exposed to the platelets due to injury, the platelets bind to collagen by surface receptors. This adhesion is stimulated by the von Willebrand factor released from endothelial cells and platelets. This forms additional cross-linking and activation of platelet integrins, which facilitate tight binding and aggregation of platelets at the site of injury. This leads to primary haemostasis.
See more: MCQs on Blood
Blood Coagulation Cascade
The process of coagulation is a cascade of enzyme catalysed reactions wherein the activation of one factor leads to the activation of another factor and so on.
The three main steps of the blood coagulation cascade are as follows:
- Formation of prothrombin activator
- Conversion of prothrombin to thrombin
- Conversion of fibrinogen into fibrin
1. Formation of prothrombin activator
The formation of a prothrombin activator is the first step in the blood coagulation cascade of secondary haemostasis. It is done by two pathways, viz. extrinsic pathway and intrinsic pathway.
Extrinsic Coagulation Pathway
It is also known as the tissue factor pathway. It is a shorter pathway. The tissue factors or tissue thromboplastins are released from the damaged vascular wall. The tissue factor activates the factor VII to VIIa. Then the factor VIIa activates the factor X to Xa in the presence of Ca2+.
Intrinsic Coagulation Pathway
It is the longer pathway of secondary haemostasis. The intrinsic pathway begins with the exposure of blood to the collagen from the underlying damaged endothelium. This activates the plasma factor XII to XIIa.
XIIa is a serine protease, it activates the factor XI to XIa. The XIa then activates the factor IX to IXa in the presence of Ca2+ ions.
The factor IXa in the presence of factor VIIIa, Ca2+ and phospholipids activate the factor X to Xa.
Common Pathway
The factor Xa, factor V, phospholipids and calcium ions form the prothrombin activator. This is the start of the common pathway of both extrinsic and intrinsic pathways leading to coagulation.
2. Conversion of prothrombin to thrombin
Prothrombin or factor II is a plasma protein and is the inactive form of the enzyme thrombin. Vitamin K is required for the synthesis of prothrombin in the liver. The prothrombin activator formed above converts prothrombin to thrombin. Thrombin is a proteolytic enzyme. It also stimulates its own formation, i.e. the conversion of prothrombin to thrombin. It promotes the formation of a prothrombin activator by activating factors VIII, V and XIII.
3. Conversion of fibrinogen into fibrin
Fibrinogen or factor I is converted to fibrin by thrombin. Thrombin forms fibrin monomers that polymerise to form long fibrin threads. These are stabilised by the factor XIII or fibrin stabilising factor. The fibrin stabilising factor is activated by thrombin to form factor XIIIa. The activated fibrin stabilising factor (XIIIa) forms cross-linking between fibrin threads in the presence of Ca2+ and stabilises the fibrin meshwork. The fibrin mesh traps the formed elements to form a solid mass called a clot.
Blood Clotting Disorders
Haemophilia is the main blood clotting disorder. Haemophilia is characterised by excessive bleeding. It is due to the absence of some of the factors required in the blood clotting cascade. The three main forms of haemophilia are as follows:
- Haemophilia A – Factor VIII deficiency
- Haemophilia B – Factor IX deficiency or “Christmas disease”
- Haemophilia C – Factor XI deficiency
Thrombosis is the formation of a blood clot inside the blood vessel. It blocks the flow of blood. Thrombosis can occur in arteries as well as veins. Arterial thrombosis affects the blood supply and leads to the damage of tissue, i.e. ischemia or necrosis. The clot may sometimes break free and circulate in the body and lead to embolism.
This was all about the Process of Blood Coagulation. Learn more about other related concepts for NEET, only at BYJUβS.
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Frequently Asked Questions
Define blood coagulation
Coagulation or clotting is defined as the process in which blood loses its fluidity and becomes a jelly-like mass a few minutes after it is shed out. It is a vital phenomenon to prevent excess loss of blood in case of injury or trauma.
What is a blood clot?
Blood clot is defined as the mass of coagulated blood which contains RBCs, WBCs and platelets entrapped in fibrin meshwork. The trapped RBCs are responsible for the red colour of the clot. The external blood clot or scab adheres to the opening of the damaged blood vessel and prevents blood loss.
What is fibrinolysis?
Lysis of blood clot inside the blood vessel is called fibrinolysis. It aids in the removal of clots from lumen of the blood vessel. This process happens in the presence of a substance called fibrinolysin or plasmin.
What are anticoagulants?
Substances which prevent or postpone coagulation of blood are called anticoagulants. Examples β EDTA and heparin. Sodium, potassium and ammonium citrates are also used as anticoagulants.
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