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Percentage of blood volume occupied by erythrocytes
Can range from 25-60% depending on species
Hematocrit
Imparts red color (depending on degree of oxygen saturation)
Hemoglobin
Colorless to yellow
Plasma
Range of 7.35 - 7.45
Blood pH
What is more acidic: Venous blood or arterial blood?
Venous blood
What is more acidic: O2 or CO2?
CO2
Less 02, more CO2
Venous blood
More O2, less CO2
Arterial blood
What is another term for red blood cells?
Erythrocytes
What is another term for white blood cells?
Leukocytes
What are the two classifications of WBCs/leukocytes?
Granulocytes and agranulocytes
What are the three granulocytes?
Neutrophils, basophils, and eosinophils
What are the two agranulocytes?
Monocytes and lymphocytes
Stay in blood for 6-20 hrs, constantly leaving blood. Stay in tissues for 2-3 days. Do not return to blood after leaving.
Granulocytes (the phils)
Stay in blood for less than 24 hours. Stay in tissues for months. Become fixed macrophages in liver, spleen, bone marrow, and lymph nodes
Monocytes
Recirculate constantly from blood to tissues, to lymph, and back to blood
Lymphocytes
How long do T cells live?
100-200 days
How long do B cells live?
2-4 days
How long do T and B cells live?
For years
What is the typical total leukocytes (wbc) count?
7000 - 15000 cells/μL
What are the neutrophil (a type of granulocyte) predominant species?
Dog, cat, horse (N is for compaNioN)
What are the lymphocyte (a type of agranulocyte) predominant species?
Cow, sheep, goat, pig (L is for Livestock)
First leukocytes (wbc) to arrive at site of acute inflammation
Very mobile
Numbers increase dramatically in acute infections
Cause phagocytosis which forms pus
Azurophilic granules supply lysosomes
Other granules produce hydrogen peroxide
Lactoferrin (sequesters iron needed for bacterial growth)
Neutrophils
When circulating, phagocytize bacteria, viruses, and antibody-antigen complexes
Leave blood in order to enter tissues, they then transform to macrophages in order to kill phagocytized microbes using acidic pH, enzymes, and hydrogren peroxide
Monocytes
Which part of the mononuclear phagocytic system (MPS) is intravascular (in blood)?
Monocytes
Which part of the mononuclear phagocytic system (MPS) is extravascular (in tissue)?
Macrophages
Which part of the mononuclear phagocytic system (MPS) are mobile cells?
Macrophages
Which part of the mononuclear phagocytic system (MPS) are fixed cells?
Kupffer cells (in liver, spleen, and lymph nodes)
Discharge granules onto opsonized parasites (parasites that have been attacked by antibodies)
Limit allergies due to the granules containing histaminase which dampens and terminates inflammatory allergic reactions
Eosinophils
Receptors for IgE (antibodies associated with allergies)
Antigen bings IgE which causes this cell to rupture, which promotes local vascular and tissue allergic reactions
Granules contain histamine, bradykinini, serotonin, and lysosomal enzymes
Low numbers in normal, healthy animals
Basophils
What are T and B cells?
Lymphocytes
What are the cell-mediated immunity cells?
T cells (the T in cell-mediaTed)
What are the humoral immunity cells?
B cells (B is for bone marrow, humerus is a bone)
Directly destroy infected or abnormal cells by recognizing specific antigens and releasing cytotoxic sybstances. Are known to attack transplated organs.
Cytotoxic T cells (killer T cells)
Coordinate the immune response by activating cytotoxic T cells and stimulating B cells
Helper T cells
Long-lived cells that remember prevoius antigens and mount a faster response upon re-exposure
Memory T cells
Proliferate after recognizing an antigen and differentiate into plasma cells and memory B cells
Activated B cells
Long-lived cells that respond rapidly to future exposure to the same antigen
Memory B cells
Produce and secrete large quantities of antibodies that bind and inactivate antigens (humoral immunity)
Plasma cells
4 globin chains, 4 heme groups (each group has iron) → can carry 4 oxygen molecules
Hemoglobin molecule
production of erythrocytes
erythropoiesis
What from the kidneys stimulates production of erythrocytes (rbc)
Erythropoietin
Immature erythrocytes (rbc) that retain some ribosomes and mature in blood after a few days. Numbers increase if RBC production is increased.
Reticulocytes
What is the RBC shape in dogs?
Biconcave disk
What is the RBC shape in goats?
Spherical
What is the RBC shape in camels?
Elliptical
What is the RBC shape in deer?
Sickle
4 globin chains, 4 hem groups, can carry 4 oxygen molecules
Hemoglobin
One heme group, one globin chain
Myoglobin
Formation of a temporary platelet plug
Primary hemostasis
Vascular damage exposes collagen in the basement membrane.
Damaged endothelial cells release fibronectin and von Willebrand factor (vWF), which promote platelet adhesion.
Step 1 of primary hemostasis: Vessel injury exposes collagen
Platelets bind exposed collagen through vWF (platelet adhesion)
Platelets extend pseudopods to capture additional circulating platelets
Step 2 of primary hemostasis: Platelets adhere to the injured site
Collagen and thrombin activate platelet receptors
Intracellular Ca2+ increases
Activated platelets synthesize and release TXA2
Step 3 of primary hemostasis: platelets become activated
TXA2 amplifies platelet activation (positive feedback)
Activated platelets release α-granules and dense granules containing coagulation factors, Ca2+, ADP, ATP, serotonin, and additional vWF
Step 4 of primary hemostasis: Platelets recruit additional platelets
Activated platelet integrins bind fibrinogen, which bridges adjacent platelets
Platelets continue to aggregate, forming a temporary platelet plug that limits blood loss until stabilized by fibrin during secondary hemostasis
Step 5 of primary hemostasis: Platelets aggregate to form temporary plug
Initiates platelet adhesion after vessel injury
Collagen
Bridges platelets to exposed collagen (adhesion)
von Willebrand factor (vWF)
Activates and recruits additional platelets
Thromboxane A₂ (TXA₂) (thanx for helping collagen)
Bridges activated platelets together (aggregation)
Fibrinogen
Reinforces platelet activation and initiates fibrin formation during secondary hemostasis
Thrombin
Formation and resolution of a stable fibrin clot
Secondary hemostasis
Thrombin converts fibrinogen into fibrin (to turn gen to rin, you need the bin)
Fibrin forms a mesh-like network that reinforces the temporary platelet plug
Blood cells become trapped within the fibrin mesh, producing a stable clot firmly attached to the vessel wall
Step 1 of secondary hemostasis: Fibrin clot forms
Platelet contractile proteins (thrombosthenin, actin, and myosin) contract, causing the clot to shrink
Serum is squeezed out of the clot, allowing more blood flow to the damaged tissue
Clot retraction reduces wound size and draws the vessel walls closer together to promote repair
Step 2 of secondary hemostasis: Clot retracts
Plasmin, an enzyme, breaks down the fibrin meshwork
The clot is gradually dissolved once healing has occured
Normal blood flow is restored through the repaired vessel
Step 3 of secondary hemostasis: Clot dissolves (fibrinolysis)
Involved in killing or inactivating antigens, and creating memory cells to respond to antigens when exposed in the future
Lymphocytes
Transforms to a macrophage before using acidic pH, enzymes, and hydrogen peroxide to kill
Monocyte
Contains cell-surface receptors for IgE and granules contain substances to enhance allergic reactions
Basophil
Granules supply lysosomal enzymes and hydrogen peroxide to digest and kill
Neutrophil
Granules contain histaminase to dampen/stop allergic reactions
Eosinophil