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Questions and Answers
Platelets primarily form a permanent plug to stop bleeding.
Platelets primarily form a permanent plug to stop bleeding.
False
Coagulation factors are mostly synthesized in the heart.
Coagulation factors are mostly synthesized in the heart.
False
The intrinsic pathway of coagulation is quicker than the extrinsic pathway.
The intrinsic pathway of coagulation is quicker than the extrinsic pathway.
False
Thrombin converts fibrinogen into fibrin, which is insoluble.
Thrombin converts fibrinogen into fibrin, which is insoluble.
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White blood cells circulate in the blood for the majority of their life span.
White blood cells circulate in the blood for the majority of their life span.
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Platelets are formed in the bone marrow and are released into the blood under the effect of thrombopoietin from the liver.
Platelets are formed in the bone marrow and are released into the blood under the effect of thrombopoietin from the liver.
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The life span of platelets is approximately 8-12 days before they are removed by tissue macrophages.
The life span of platelets is approximately 8-12 days before they are removed by tissue macrophages.
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Platelets contain only one type of granule that is responsible for hemostasis.
Platelets contain only one type of granule that is responsible for hemostasis.
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Platelet-derived growth factor (PDGF) plays a role in the healing of injured endothelium.
Platelet-derived growth factor (PDGF) plays a role in the healing of injured endothelium.
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Hemostasis is the process that involves the increased fluidity of blood to prevent clot formation.
Hemostasis is the process that involves the increased fluidity of blood to prevent clot formation.
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Study Notes
Blood Components and Their Functions-2
- The presentation is about blood components and their functions, specifically focusing on platelets.
-
Platelets (Thrombocytes):
- Shape: Minute round or oval discs (2-4 μm), non-nucleated, size can increase to 6 μm after activation.
- Number: 150,000 – 400,000/mm³.
- Formation: Formed in the bone marrow as buds on the surface of megakaryocytes, released into the bloodstream under the influence of thrombopoietin from the kidney.
- Life span: 8-12 days, then removed by tissue macrophages.
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Platelet Structure:
- Outer coat: Mucopolysaccharide surface coat, crucial for adhesion and aggregation. Glycoproteins bind to Von Willebrand Factor (vWF), necessary for adhesion to damaged endothelial cells; also acts as fibrinogen receptors.
- Plasma membrane: Basis structure of platelet factor 3 (PF3).
- Cytoskeleton (under the membrane):
- Microfilaments: Composed of actin, myosin, and thrombasthenin.
- Microtubules: Maintain the disc shape of the platelets.
- Granules: Three types:
- Dense granules: Small, contain nucleotides (ADP), serotonin, and calcium.
- Specific (Alpha) granules: Large, contain platelet factors responsible for hemostasis.
- Dense tubular system: Contains calcium; site for prostaglandin and thromboxane A2 synthesis; regulates platelet activation by sequestering or releasing calcium.
- Other components: Mitochondria, glycogen, and lysosomes containing hydrolytic enzymes.
Functions of Blood Platelets
- Form temporary hemostatic plugs (platelet adhesion, activation, and aggregation).
- Release serotonin and thromboxane A2.
- Crucial for blood coagulation (supplying platelet factor III and factor XIII).
- Cause clot retraction.
- Release platelet-derived growth factor (PDGF) for healing injured endothelium.
Hemostasis
- Stoppage of bleeding by forming blood clots and maintaining blood fluidity in the vascular system.
- Three main components:
- Vasoconstriction: Contraction of smooth muscle in vessel walls (vascular spasm).
- Platelet aggregation: Platelets adhere to exposed collagen fibers in damaged blood vessels, releasing chemicals to cause aggregation (temporary platelet plug).
- Coagulation (blood clotting): Occurs via clotting factors (proteins, mostly synthesized in the liver).
Blood Coagulation
- Essential process because aggregation and vasoconstriction alone are not enough to stop bleeding entirely.
- Involves clotting factors that work together to transform fibrinogen into fibrin, forming a clot.
- Two pathways to blood clot formation: Intrinsic and extrinsic pathways.
White Blood Cells (WBCs)
- Circulate briefly in the bloodstream, predominantly migrating through body tissues.
- Migrate from blood vessels through extravasation.
- Some WBCs (neutrophils, eosinophils, monocytes) exhibit phagocytosis.
Types of White Blood Cells (WBCs)
- Classified into granulocytes (include neutrophils, eosinophils, basophils) and agranulocytes (include lymphocytes—B and T lymphocytes and natural killer cells, and monocytes).
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Description
This quiz explores the essential components of blood with a particular focus on platelets (thrombocytes). Learn about their structure, formation, lifespan, and functions in the body. Discover how platelets play a crucial role in the healing process and blood clotting.