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111 Cards in this Set

  • Front
  • Back
Three general functions of Blood
Transportation
Regulation
Protection
Blood Volume in average sized adult Male & Female
Male 5-6 Liters

Female 4-5 Liters
Venipuncture
Withdrawal of blood from a vein by using a needle and collecting tube
Finger/Heel stick
Process of blood withdrawal used for diabetics and infants
Arterial Stick
Process of blood withdrawal from arteries to test oxygen in oxygenated blood
Buffy Coat
Thin layer between packed RBCs and plasma in centrifuged blood
Function of Plasma Proteins
Proteins in blood that plays an important role in diffusion of fluids across capillaries
Where are Plasma Proteins synthesized
Synthesized by Hepatocytes in the liver
3 Types of Plasma Proteins and their functions
Albumins - Most numerous functions as transport proteins for several steroid hormones and for fatty acids

Globulins - Develops from B lymphocytes. Alpha and beta transport iron lipids and vitamins. Gamma Proteins help attack viruses and bacteria

Fibrinogen - Produced by liver for blood clotting
3 Formed elements of Blood
RBCs
WBCs
Platelets
Hematocrit & Average for male and Females
Percentage of total blood volume occupied by RBCs

Male - 47%
Female - 42%
Polycythemia
Condition that involves abnormally high hematocrit level causing the heart to pump harder
Hemocytoblasts
a.k.a Pluripotent stem cells which have the capacity to develop into several different types of cells
Where are Bone Marrow Examination samples taken from?
Iliac crest of hip bone & sometimes sternum
Progenitor Cells
Cells that are sometimes developed from Myeloid stem cells which are no longer capable of reproducing themselves but are committed to giving rise to more specific blood elements

- No recognizable microscopic appearance
Precursor Cells
a.k.a Blasts that have recognizable microscopic apearances
Hemopoietic Growth Factors and the 3 types
- Hormones that regulate differentiation and proliferation of particular progenitor cells
Erythropoitin & its production
A hemopoietic growth factor produced by cells in the kidney that increases number of RBC precursors
Thrombopoietin & its production
A Hemopoietic growth factor produced by liver and stimulates formation of platelets from megakaryocytes
Cytokines & Two families
A Hemopoietic growth factor that are produced by red bone marrow, leukocytes, macrophages, fibroblasts, endothelial cells that help to regulate activities of cells in nonspecific defenses and immune responses

- CFUs and Interleukins
How does Hemoglobin help regulate BP?
Hemoglobin transports NO produced by endothelial cells which cause vasodialation
Formaion and destruction of RBC
RBC - Globin - AminoAcids

RBC - Heme - Fe3+ - Transferrin to Liver - Stored as Ferritin - Transferrin to bone - Iron + Globin + Vitamin B12 + Erthopoietin = Erythropoiesis

Heme - Biliverdin - Bilirubin which goes into blood then liver - Secreted into bile inside liver to small intestine then large - Bacteria in large intestine convert bilirubin into urobilinogen - Some become yellow urobilin to be secreted in urine - most urobilinogen is converted to pigment stercobilin which gives feces its color
Transferrin
Transporter for Iron in the Blood
Ferritin
Iron storage protein found in Liver
Biliverdin
Green Pigment found during phagocytosis which gets further converted later
Bilirubin
Yellow pigment found during phagocytosis which is then brought into the liver
Iron Overload
Condition where amount of iron builds up and saturates all of the Ferritin and Transferrin, allowing the free growth of iron dependent microbes
Erythropoiesis
Production of RBCs
Proerythroblast
Precursor cell which divides into cells that synthesize hemoglobin
Reticulocyte
Cell that has ejected its nucleus & Becomes a RBC in a couple of days
Hypoxia
Cellular oxygen Deficiency
Cells developed from Myeloid Stem Cells (6)
RBC, Platelet, Eosinophil, Basophil, Neutrophil, Monocyte
Cells developed from Lymphoid Stem Cells (2)
T Lymphocyte (Tcell), B Lymphocyte (Bcell)
Granular Leukocytes
Eosinophil, Basophil, Neutrophil
Eosinophil
Dyes red orange in Acidic dye & nucleus has two lobes connected by a thick srand of chromatin
Basophil
Stains blue purple in Basic Dye. Granules obscures nucleus which has two lobes
Neutrophil
Pale lilac & has 2-5 lbes connected by thin strands of chromatin
Lymphocyte
Nucleus is round or indented and Stains dark
Monocyte
Nucleus is kidney or horseshoe shaped and cytoplasm is blue grap due to it's azurophilic granules which are lysosomes
Macrophages & two types
Monocytes differentiated in tissues

Fixed Macrophages reside in a particular tissue

Wandering Macrophage roam tissues and gather at sites of infection or inflammation
Major Hisocompatibility antigens
MHC, proteins found on WBCs and all other nucleated cells that serve as cell ID markers that are unique for each person except twins
Leukocytosis
An Increased number of WBCs as a protective response to microbes, anesthesia, excercise, and surgery
Leukopenia
A Decreased number of WBCs that is never beneficial
Which cells return to bloodstream after fighting and which don't
Granulocytes and Monocytes never return but Lymphocytes continually recirculate from blood to interstitial spaces
Emigration
aka Diapedesis which is a process where WBCs roll along endothelium, stick to it, and then sqeeze between endothelial cells
Adhesion Molecules & 2 examples
Molecules that help WBCs stick to endothelium

Selectins - displayed by endothelial cells in response to injury and sticks to carbs on surface of neutrophils causing it to slow down and roll

Integrin - Found in Neutrophil surface to stick it to endothelium and help it to move through blood vessel
Which WBCs are active in phagocytosis?
Neutrophils and Macrophages
Kinin
Toxin produced by microbes which stimulate chemotaxis
Which WBC responds to tissue destruction by bacteria most quickly? And is the most numerous?
Neutrophils
Proteins found in neutrophil vesiclesthat poke holes in microbe membranes
Defensin
Neutrophil Method of Action
Arrives first and Engulfs the pathogen while releasing chemicals such as lysozyme, strong oxidants, and defensin to poke holes and splatter it.
Monocyte Method of Action
Take longer to reach site of infection but comes in large numbers to destroy more microbes and clean up cellular debris
Basophil Method of Action
Leaves capillaries and releases granules containing heparin, histamine, and serotonin which intensify the inflammatory response
Eosinophil Method of Action
Leaves capillaries and releases enzymes such as histaminase that combats histamine. Also phagocytizes antigen-antibody complexes and effective against parasitic worms
Lymphocyte 3 types and Methods of Action
B cells are effective at destroying bacteria and inactivating their toxins

T cells attack viruses, fungi, cancer cells

NK cells attack wide variety of microbes and spontaneous tumor cells
A count of each of the five types of WBCs
Differential WBC count
High Neutrophil Count & Normal
Bacterial infection

60%-70% Normal
High Lymphocyte Count & Normal
Viral infection

20%-25% normal
High Monocyte Count & Normal
Fungal/Viral infection

3%-8%
High Eosinophil Count & Normal
Parasite or Allergy

2%-4%
High Basophil Count & Normal
Allergic reaction

<1%
Thrombopoietin
Hormone that stimulates Myeloid Stem cells to develop in to Megakaryocyte-colony-forming cells
Thrombocyte
A.K.A Platelet which are tiny fragments of Megakaryocytes that are enclosed in a piece of the plasma membrane
Bone Marrow Transplant
Replacement of cancerous or abnormal red bone marrow with healthy red bone marrow
Cord-Blood Transplant
Obtaining stem cells from the umbilical cord after birth
Hemostasis
Sequence of responses that stops bleeding
Hemorrhage
Loss of a large amount of blood
Vascular Spasm
Contraction of the smooth muscle in walls of arteries and arterioles after being damanged
Platelet-Derived Growth Factor
A hormone inside platelets that causes proliferation of vascular endothelial cells, smooth muscle fibers, and fibroblasts to help repair damaged blood vessel walls
Steps to Platelet plug formation
1) Plate Adhesion
2) Platelet release reaction
3) Platelet Aggregation
Mass of platelets that block the site of wound
Plate Plug
Serum
Blood plasma minus clotting proteins
Clot
A network of insoluble protein fibers called fibrin which traps formed elements of blood
Coagulation
a.k.a Clotting which is a series of chemical reactions that culminates in formation of fibrin threads
Thrombosis
Condition in which blood clots too easily which could block undamaged blood vessels
Extrinsic Pathway of Blood Clotting
Has fewer steps than intrinsic pathway and occurs rapidly

- Tissue factor (TF) a.k.a Thromboplastin is released by damaged cells and falls into blood to combine with calcium to activate factor X which then combines with factor V in presence of Ca2+ to form prothrombinase
Intrinsic Pathway of Blood Clotting
- Occurs slowly

- When endothelial cells become damaged, blood comes into contact with collagen fibers in endothelium or glass wall of a tube which activates clotting factor 12 which then activates clotting factor X which in the presence of Calcium combines with factor V to form prothrombinase.

- Damage to endothelial cells damages platelets causing them to release phospholipids which can combine with calcium ions to also activate factor X
Common Pathway
Prothrombinase and calcium converts prothrombin into thrombin, thrombin with calcium converts fibrinogen to fibrin, Thrombin also activates factor 13 which strengthens the fibrin
Two positive feedback loops of Thrombin
1) Involves factor V and accelerates formation of prothrombinase which in turn produces more thrombin

2)Thrombin activates platelets which releases more platelet phospholipids which combines with calcium to activate factor X and so on
Clot Retraction
Process in which platelets pull on fibrin threads to bring edges of damaged vessel closer to decrease risk of further injury. This depends on clotting factor XIII released by platelets in the clot
Vitamin K and Blood Clotting
Vitamin K is a fat soluble vitamin produced by bacteria and absorbed through large intestine. It is not directly involved in clotting but is responsible for synthesis of 4 clotting factors
Fibrinolytic System
System that dissolves small inappropriate clots and clots after damage is repaired
Dissolving of a clot
Fibrinolysis
Plasminogen
Inactive enzyme that is incorporated into a clot when it forms
Plasmin
a.k.a Fibrinolysin is the active plasma enzyme form of plasminogen which digests fibrin threads and deactivates fibrinogen, prothrombin, factors V and XII to stop the clot
Why doesn't a clot spread beyond a wound site? 2 Reasons
1) Fibrin absorbs thrombin into the clot

2) Clotting factors are too dispersed by blood to bring about widespread clotting
Prostacyclin
A prostaglandin released by endothelial cells and WBCs that inhibits platelet adhesion and release
Substances that delay, supress, or prevent blood clotting
Anticoagulants
An anticoagulant that blocks action of clotting factors X, XII, and Prothrombin
Antithrombin
An anticoagulant that is produced by mast cells and basophils and combine with Antithrombin to increase it's effectiveness in blocking thrombin
Heparin
Anticoagulant that enhances activity of plasminogen activators and blocks 2 major clotting factors that Antithrombin does not
Activated Protein C (APC)
Warfarin
Antagonist to Vitamin K and blocks synthesis of the 4 clotting factors that Vitamin K produces
Thrombus
The inappropriate clot formed by thrombosis
A blood clot, bubble of air, fat from broken bones, or any piece of debris transported by blood stream
Embolus
Pulmonary Embolism
Condition in which a Embolus lodges in the lungs
StreptoKinase
Enzyme produced by streptococcal bacteria which activates plasminogen
Tissue Plasminogen Activator t-PA
A genetically engineered version of this is used to treat victims of heart attacks and strokes caused by blood clots
Hemolytic Disease of the Newborn (HDN)
Disease when mother is Rh- and baby is Rh+ so during birth their bloods contact causing the mother to make anti-Rh antibodies so during second pregnancy it will attack the baby's RBCs. Doesn't occur with first baby because blood only comes in contact during birth.
RhoGAM
Anti-Rh Gamma Globulin which binds to the Rh antigens of the baby to inactivate them so mother's blood never sees them
Cross Matching
Donor's RBCs are mixed with recipient's serum to see if agglutination occurs.
Anemia
Condition in which the oxygen carrying capacity of blood is reduced
Iron Deficiency Anemia
Most common form of Anemia due to the lack of Iron and more prevalent in Women due to demands of fetus and menstruation
Megaloblastic Anemia
Condition caused by inadequate vitamin B12 or Folic acid which causes red bone marrow to produce large abnormal RBCs (Megaloblasts)
Pernicious Anemia
Condition due to inadequate hemopoiesis resulting from inability of the stomach to produce intrinsic factor which is needed to absorb vitamin B12 in small intestine
Hemorrhagic Anemia
Anemia due to excessive loss of RBCs from large wound or heavy menstruation
Hemolytic Anemia
Condition where RBC plasma membranes rupture prematurely causing hemoglobin to pour out into plasma and damage the kidneys
Thalassemia
Condition in which there is a deficient synthesis of hemoglobin
Aplastic Anemia
Condition caused by destruction of Red Bone Marrow due to toxins, radiation or medications
Abnormal type of Hemoglobin found in RBCs of a person with Sickle Cell Anemia
Hb-S
Hemophilia
Condition in which there is a deficiency in clotting causing severe bleeding in only minor trauma
Leukemia
Condition in which there is a large multiplication of cancerous WBCs which inhibit production of RBCs, normal WBCs, and platelets