White blood cells: Neutrophils60%-70%, Lymphocytes 20%-25%, Monocytes3%-8%, Eosinophils 2%-4%, Basophils0.5%-1%
Red blood cells: 4.2-6.2million
Formedelements: 45%
Plasma: 55%, Proteins7%, Water91%, Othersolutes2%
Formed elements (number per cubic mm): Platelets 250-400 thousand, White blood cells 5-10 thousand
Plasma
55% of total blood, pale, yellow liquid that surrounds cells, 91% water, 7% proteins, and 2% other
Formed Elements
45% of total blood, cells and cell fragments, erythrocytes, leukocytes, thrombocytes
Plasma Proteins
Albumin: 58% of plasma proteins, helps maintain water balance
Globulins: 38% of plasma proteins, helps immune system
Fibrinogen: 4% of plasma proteins, aids in clot formation
Erythrocytes (Red blood cells)
Disk-shaped with thick edges, Nucleus is lost during development, Live for 120 days, Function: transport O2 to tissues
Hemoglobin
Main component of erythrocytes, Transports O2, Each globin protein is attached to a heme molecule, Each heme contains one iron atom, O2 binds to iron, Oxyhemoglobin: hemoglobin with an O2 attached
Production of Erythrocytes
1. Decreased blood O2 levels cause kidneys to increase production of erythropoietin
2. Erythropoietin stimulates red bone marrow to produce more erythrocytes
3. Increased erythrocytes cause an increase in blood O2 levels
Fate of Old Erythrocytes and Hemoglobin
1. Old rbc's are removed from blood by macrophages in spleen and liver
2. Hemoglobin is broken down
3. Globin is broken down into amino acids
4. Hemoglobin's iron is recycled
5. Heme is converted to bilirubin
6. Bilirubin is taken up by liver and released into small intestine as part of bile
Leukocytes (White blood cells)
Lack hemoglobin, Larger than erythrocytes, Contain a nucleus, Functions: fight infections, remove dead cells and debris by phagocytosis
Types of Leukocytes
Granulocytes: Neutrophils, Eosinophils, Basophils
Agranulocytes: Monocytes, Lymphocytes
Platelets
Blood clotting cells, produced in red bone marrow
Hematopoiesis
Process of blood cell formation, In an infant occurs in liver, thymus gland, spleen, lymph nodes, and red bone marrow, In adults occurs mainly in red bone marrow, Stem cell: original cell line
Blood Loss
When blood vessels are damaged, blood can leak into other tissues and disrupt normal function, Blood that is lost must be replaced by production of new blood or by a transfusion
Preventing Blood Loss
Vascular spasm: temporary constriction of blood vessel
Platelet plugs: can seal up small breaks in blood vessels
Blood clotting (coagulation)
Blood Clotting
Blood can be transformed from a liquid to a gel, Clot: network of thread-like proteins called fibrin that trap blood cells and fluid, Clotting factors: proteins in plasma, only activated following injury, made in liver, require vitamin K
Three-Phase Process of Hemostasis
1. Phase 1: Vascular spasm constricts the vessel
2. Phase 2: Platelets stick together plugging the site
3. Phase 3: Clot formation starts: 1. Enzyme cascade results in activation of Factor X, 2. Factor X converts prothrombin in plasma to thrombin, 3. Thrombin converts fibrinogen, a plasma protein, to fibrin threads, 4. Fibrin forms a net that entangles cells and platelets, forming a clot
Steps in Clot Formation
1. Injury to a blood vessel causes inactive clotting factors to become activated due to exposed conn. tissue or release of thromboplastin
2. Prothrombinase (clotting factor) is formed and acts upon prothrombin
3. Prothrombin is switched to its active form thrombin
4. Thrombin activates fibrinogen into its active form fibrin
5. Fibrin forms a network that traps blood (clots)
Control of Clot Formation
Clots need to be controlled so they don't spread throughout the body, Anticoagulants: prevent clots from forming, Ex. Heparin and antithrombin, Injury causes enough clotting factors to be activated that anticoagulants can't work in that particular area of the body
Clot Retraction and Fibrinolysis
1. Clot retraction: condensing of clot, serum in plasma is squeezed out of clot, helps enhance healing
2. Fibrinolysis: process of dissolving clot, plasminogen (plasma protein) breaks down clot (fibrin)
Blood Reactions
Injury or surgery can lead to a blood transfusion, Transfusion reactions/Aggulination: clumping of blood cells (bad), Antigens: molecules on surface of erythrocytes, Antibodies: proteins in plasma
ABO Blood Groups
Type A, Type B, Type AB, Type O
Antigen: A, B, A&B, None
Antibodies: Anti-B, Anti-A, None, Anti-A&B
Common: 2nd, 3rd, 4th, 1st
Blood Type Compatibility
O are universal donors because they have no antigens
Type A can receive A and O blood
Type B can receive B and O blood
Type AB can receive A, B, AB blood
Type O can only receive O blood
Agglutination: Clumping of foreign cells by plasma proteins, When blood of incompatible types mixes, the immune system attacks the unfamiliar molecules
Rh Blood Group
Rh positive means you have Rh antigens, 95-85% of the population is Rh+, Antibodies only develop if an Rh- person is exposed to Rh+ blood by transfusion or from mother to fetus
Example of Rh Reaction
If mother is Rh- and fetus is Rh+ the mother can be exposed to Rh+ blood if fetal blood leaks through placenta and mixes with mother's blood, First time this occurs mother's blood produces antibodies against antigens, Any repeated mixing of blood causes a reaction
Hemolytic Disease of Newborn
Occurs when mother produces anti-Rh antibodies that cross placenta and agglutination and hemolysis of fetal erythrocytes occurs, Can be fatal to fetus, Prevented if mother is treated with RhoGAM which contains antibodies against Rh antigens
Diagnostic Blood Tests
Complete blood count, Hematocrit, Hemoglobin, Prothrombin time, White blood cell count, White blood cell differential count