Ch. 19 Cardiovascular system: The Blood
Monocytes
(Blue-Gray cytoplasm and Kidney shaped nucleus) -Differentiate into: ~Fixed Macrophages ~Wandering Macrophages
Lymphocytes
(Tiny, Stains dark) -T Cells -B cells -Natural Killer (NK) Cells
Blood typing
-Agglutination= clumping of RBC's (different than clotting) -Anti-A serum -Anti-B serum
Major Soldiers of immune system: Lymphocytes
-B cells -Develop into plasma cells, whic secret antibodies -Attacks bacteria -T cells -Attacks viruses, cancer cells, and transplanted tissues -Killer cells -Attack spontaneously arising tumor cells
Red Blood Cell Anatomy
-Biconcave discs -Lack nucleus and other organelles -Contain hemoglobin -Plasma Membranes ~Contain different glycolipids ~Antigens that account for various blood types
Basophils
-Blue-Purple granules -Nucleus usually not clearly visible
Coagulation
-Coagulation phase --Blood clotting -Actually a series of events -Clotting factors -Cascade of events: -Extrinsic pathway -Intrinsic pathway -Common pathway -Clot retraction
Red Blood Cell Physiology
-Contains no nucleus ~Therefore large surface area to transport oxygen -ATP generation- anaerobic ~Don't use the oxygen they transport -Shape of RBC ~Larger surface area for gas diffusion
Vascular spasm
-Contraction of vessel walls of damaged arteries or arterioles -Occurs immediately
Clot retraction
-Control of Hemostasis -Consolidation or tightening of fibrin clot -Pulls edges of damaged vessel closer together -Permanent repair takes place
Dissolution of Clot
-Control of Hemostasis -Fibrinolysis - dissolution of a clot -Pasminogen --> plasmin --> dissolves clot -Plasmin -Digests fibrin thread -Inactivates fibrinogen, prothrombin, and Factors V, VIII, and XII
Common pathway
-Development to Thrombin and Fibrin -Prothrombinase + Ca2+ converts Prothrombin --> Thrombin -Thrombin + Ca2+ --> fibrinogen --> fibrin -Thrombin also activates Factor XIII which strengthens fibrin threads into clot
Hemoglobin Structure
-Each RBC contains millions -Structure: Globin ~4 polypeptide chains (2 Alpha) (2 Beta) ~4 hemes (Fe2+)
Intrinsic pathway
-More complex; occurs w/in blood -Damage to endothelial cells exposes collagen fibers --> contact with collagen fibers activates Factor XII -Activated Factor XII + Ca2+ --> Factor X -Activated platelets --> platelet phospholipids + Ca2+ --> Factor X -Factor X + Ca2+ --> prothrombinase
Function of White Blood Cells
-Most WBC have a life span of only a few days -infection=only few hours -Normal Leukocyte levels (WBC Count) -5,000-10,000 cells per uL -Outnumbered by RBC's 700:1 -Combat pathogens -Phagocytosis -Immune Responses
Extrinsic pathway
-Occurs when blood has escaped into surrounding tissues -Tissue factor (TF) + Ca2+ --> Factor X + Factor V + ca2+ --> prothrombinase
Antigens (agglutinogens)
-On surface of erythrocytes -Blood groups based on presence or absence -Within blood groups, there may be 1-2 Blood types -Common blood groups: -ABO -Rh
Blood types and associated antigents
-Only Antigen A = Blood type A -Only Antigen B = Blood type B -Both Antigens A & B = Blood type AB -Neither Antigens A or B = Blood type O
Antibodies of Blood
-Opposites of Antigens -Won't have antibodies against own blood type/antigen -Antigen A/Type A= Antibodies B -Antigen B/Type B= Antibodies A -Antigens A&B/Type AB= No antibodies (universal recipients) -No Antigens/Type O= Antibodies A & B (universal donors)
Neutrophils
-Pale Lilac granules -Two to Five lobed nucleus -Neutrophils age=increase in nuclear lobes
Platelet phase (developing of platelet plug
-Platelet adhesion -Platelet release reaction -Platelet aggregation --Platelet plug formed
Eosinophils
-Red-Orange granules -Two-lobed nucleus
Rh Blood Group
-Rh antigen=Rh+ -No Rh antigen=Rh-
Hemostasis
-Sequence of responses to stop bleeding (involves platelets) -Three mechanisms contribute to hemostasis: 1. Vascular spasm 2. Platelet plug 3. Coagulation
Chemotaxis
1. Movement of cells or organisms in response to chemicals, whereby the cells are attracted (positive chemotaxis) or repelled (negative chemotaxis) by substances exhibiting chemical properties. 2. The migration of polymorphonuclear leukocytes and macrophages toward higher concentrations of certain fragments of complement.
Red Blood Cell Life Cycle (120 Days)
1. Phagocytosis of RBC ~Macrophages in spleen, liver, or red bone marrow 2. Hemes and globins separated: 3. Globin is a protein -Reused for protein synthesis ~Heme seperates into (Iron)-Fe3+ (Biliverdin) 4. Iron removed from heme (Fe3+) binds to transferrin -Fe3+ detaches from transferrin (carries Fe3+ in blood & attaches to ferritin (stores Fe3+ in liver) -Fe3+ reattaches to transferrin -Transferrin transports Fe3+ to bone marrow where it is recycled -Erythropoiesis --> RBC --> enter circulation 5. Non-iron portion of heme converted to biliverdin (green) then into bilirubin (yellow) -Bilirubin transported to liver -Bilirubin secreted by liver cells into bile --> sm intestine --> lg intestine -In lg intestin, converted to urobilinogen ~converted to urobilin (yellow)-excreted in urine ~converted to stercobilin (brown)- eliminated in feces
Blood Plasma Contents
1. Water (91.5%) 2. Proteins (7.0%) -Albumins (54%) -Globulins (38%) -Clotting proteins (7%) -Antibodies (sometimes) 3. Other Solutes (1.5%) -Electrolytes -Nutrients -Gases -Regulatory substances -Waste products
Formed Elements Contents
1. Whole Blood Cells -Red Blood Cells (RBC's)-Erythrocytes -White Blood Cells (WBC's)-Leukocytes ~Granular (Basophils, Eosinophils, Neutrophils) ~Agranular (Lymphocytes and Monocytes) 2. Fragments -Platelets - thrombocytes
Biliverdin
A green bile pigment formed from the oxidation of heme; a bilin with a structure almost identical to that of bilirubin.
RBC
A normal, mature RBC has no nucleus and is only about 7.5 μm in diameter. More than 1500 of them could be placed side by side in a 1 cm space. Before the cell reaches maturity and enters the bloodstream from the bone marrow, the nucleus is extruded, mature RBCs are shaped like tiny biconcave disks, does not contain ribosomes, mitochondria, and other organelles typical of most body cells, primary component of each RBC is the red protein pigment, hemoglobin. It accounts for more than one third of the cell volume and is critically important to its primary function.
Progenitor cell
A progenitor cell is a biological cell that, like a stem cell, has a tendency to differentiate into a specific type of cell, but is already more specific than a stem cell and is pushed to differentiate into its "target" cell.
Pluripotent stem cell
Pluripotent stem cells are master cells. They're able to make cells from all three basic body layers, so they can potentially produce any cell or tissue the body needs to repair itself. This "master" property is called pluripotency. Like all stem cells, pluripotent stem cells are also able to self-renew, meaning they can perpetually create more copies of themselves.
Function of RBC
RBCs play a critical role in the transport of oxygen and carbon dioxide in the body
Stercoblin
Stercobilin is a tetrapyrrolic bile pigment and is one end-product of heme catabolism. It is the chemical responsible for the brown color of human feces and was originally isolated from feces in 1932
Clotting factors
Substances in the blood that act in sequence to stop bleeding by formin, the chemical and cellular constituents of the blood responsible for the conversion of fibrinogen into a mesh of insoluble fibrin causing the blood to coagulate or clot.
Blood plasma
The fluid portion of blood; one of the three major body fluids (interstitial and intracellular fluids are the other two). Totals about 55% of blood volume.
Urobilinogen
Urobilinogen is a colourless by-product of bilirubin reduction. It is formed in the intestines by bacterial action on bilirubin.
Thrombopoietin
a colony-stimulating factor that is the humoral regulator of the production of platelets.
Platelet
a small colorless disk-shaped cell fragment without a nucleus, found in large numbers in blood and involved in clotting.
Precursor cell
also called a blast cell or simply blast, is a type of partially differentiated, usually unipotent cell that has lost most or all of the stem cell multipotency. Usually a precursor cell is a stem cell which has the capacity to differentiate into only one cell types.
Agranular leukocyte
also known as mononuclear leukocytes, are white blood cells with a one-lobed nucleus. They are characterized by the absence of granules in their cytoplasm, which distinguishes them from granulocytes. Normal hematologic blood values of MLs are about 35% of all white blood cells.
Transfusion
an act of transferring donated blood, blood products, or other fluid into the circulatory system of a person or animal.
Agglutinogen
an antigen that stimulates the production of an agglutinin.
Leukocytosis
an increase in the number of white cells in the blood, especially during an infection.
Globin
chain of four proteins; binds to a red pigment (heme) to form hemoglobin
Cytokines
chemical released from cells to trigger or regulate innate and adaptive immune responses
Thrombopoietin
glycoprotein hormone produced by the liver and kidney which regulates the production of platelets. It stimulates the production and differentiation of megakaryocytes, the bone marrow cells that bud off large numbers of platelets.
Erythropoietin
glycoprotein secreted to increase red blood cell production in response to oxygen deficiency
Heme
iron-containing chemical group found in hemoglobin; temporarily binds to oxygen
Hemoglobin
iron-containing protein in red blood cells responsible for their oxygen-carrying capacity. Packed within each RBC are an estimated 200 to 300 million molecules of hemoglobin, which make up about 95% of the dry weight of each cell. Each hemoglobin molecule is composed of four protein chains. Each chain, called a globin, is bound to a red pigment, identified in Figure 20-5, as a heme group. Each heme group contains one iron atom. Therefore one hemoglobin molecule contains four iron atoms.
Thrombosis
local coagulation or clotting of the blood in a part of the circulatory system.
Hematopoiesis
process of blood cell formation
Erythropoiesis
process of red blood cell formation
Phagocytosis
the engulfing of microorganisms or other cells and foreign particles by phagocytes
Fibrinolysis
the enzymatic breakdown of the fibrin in blood clots.
Emigration
the escape of leukocytes through the walls of small blood vessels; diapedesis.
Hemolysis
the rupture or destruction of red blood cells.
Granular leukocyte
they are better known as granulocytes -- are part of the innate immune system and have somewhat non specific, broad-based activity. They do not respond exclusively to specific antigens, as do B-cells and T-cells. Neutrophils, eosinophils and basophils are all types of granulocytes.
Hematocrit
volume percent of blood cells in whole blood; packed cell volume
Bilirubin
yellowish pigment formed when the heme group is removed from the hemoglobin molecule and stripped of its iron atom; a product of the breakdown of red blood cells