Composition of blood
1. Connective tissue with liquid matrix (plasma) and
formed elements (cells)
2. Hematocrit when blood is spun
in a centrifuge heavier RBC (bottom)
3. Erythrocytes (RBC) take up 45% volume in a normal hematocrit
4. Plasma takes up 55% volume in normal hematocrit
5. Buffy Coat whitish layer at RBC plasma border; WBCs and platelets
Function of blood
1. Distribution nutrients, waste, oxygen, carbon dioxide,
hormones
2. Thermoregulation capillaries in skin; cool body off or
retain heat
3. Clotting prevents blood loss
4. Infection protection antibodies, cellular defenses
5. Fluid volume salts and albumin prevent fluid loss;
maintain vascular volume
Composition of plasma
1. Proteins - include
-a. Albumin 60%; osmotic pressure to keep fluid in blood
-b. Antibodies or gamma globulins; immunity
-c. Clotting proteins prothrobin
and fibrinogen
2. Others - include
-a. Nutrients such as blood glucose
-b. Electrolytes most notably sodium ion
Erythrocytes
1. Structure related to function
-a. Anucleate lack nucleus and
other cellular organelles; bags of hemoglobin
-b. Biconcave concave on both sides; optimum increase in
surface area
2. Hemoglobin red pigment; carries oxygen
-a. Globin 4 polypeptide chains;
2 alpha; 2 beta
-b. Heme iron containing
compound; one associated with each globin
3. Function - of red blood cell and hemoglobin
-a. Oxyhemoglobin one molecule
of oxygen binds to the iron in each heme
-b. Carbaminohemoglobin carbon
dioxide binds with amino acid of globin
Hematopoiesis
1. Defined general term for blood cell formation
2. Red bone marrow where it takes place; axial; girdles
3. Hematopoetic stem cell (hemocytoblast) all formed elements come from
Erythropoiesis
1. Defined formation of erythrocytes
2. Hemocytoblast forms all
formed elements
3. Proerythroblast rabid
dividing; all decedents are erythrocytes
4. Erythroblast ribosomes to
produce hemoglobin
5. Normoblast much hemoglobin;
later nucleus degenerates and ejected
6. Reticulocytes still some ribosomes; enter blood stream like this
7. Erythrocytes ribosomes
degraded after about 2 days
Regulation and requirements of erythropoesis
1. Negative feedback mechanism in homeostasis; acts
against the stimulus
2. Hypoxia low blood oxygen level; stimulates kidney
3. Erythropoietin hormone released by kidney targets red
bone marrow
4. Red bone marrow erythrocyte production is stimulated;
blood oxygen increases
5. Requirements iron, B complex vitamins, and amino acids
Fate of erythrocytes
1. Life span up to 120 days; no nucleus, no long term
maintenance
2. Spleen in small capillaries RBCs
consumed by macrophages
3. Bilirubin yellow pigment;
remnant of heme; released in bile
4. Globulin broken down to amino acids; recycled to blood
Erythrocyte disorders: anemias
1. Anemia low RBCs or hemoglobin
2. Hemorrhagic anemia low number of RBCs
resulting from blood loss
3. Hemolytic anemia RBCs
prematurely destroyed; transfusion mismatch
4. Aplastic anemia hemopoietic components destroyed; radiation; other problems
5. Iron deficiency anemia decreased hemoglobin due to lack
of iron
6. Athletes anemia exercise caused increased blood
supply; dilutes blood
7. Pernicious anemia vitamin B-12 deficiency; rarely
result of diet
-a. Intrinsic factor produced by stomach; B-12 absorption;
less in old age
8. Thalassemias genetic;
9. Sickle cell anemia genetic;
Erythrocyte disorders: polycythemias
1. Polycythemia high RBCs
2. Polycythemia vera usually bone marrow cancer;
80% RBCs
3. Secondary polycythemia
usually from high altitudes; high erythropoietin
Leukocytes
1. True cells have nucleus and other cellular organelles
2. Protection both nonspecific and immune response to
pathogens
3. Leukocytosis over 11,000;
hours after bacteria or viral infection
4. NLMEB - neutrophils, lymphocytes, monocytes,
eosinophils, and basophils
5. Classification two main groups
-a. Granulocytes membrane bound granules; lobed nuclei
-b. Agranulocytes membrane bound
granules not apparent
Granulocytes
1. Neutrophils
-a. Cytoplasm pale lilac; both acidic and basic stains
-b. Nucleus
-c. Function phygocytosis
(mostly bacteria)
2. Eosinophils
-a. Cytoplasm brick red; acidic dyes; lysosome
like digestive enzymes
-b. Nucleus two lobed; like old telephone receivers
-c. Function parasitic worms; allergy
3. Basophils
-a. Cytoplasm blue purple; basic dyes; histamine
-b. Nucleus S or U shaped
-c.
Function release histamine; this brings about inflammation
Agranulocytes
1. Lymphocyte immune response; found in lymphoid tissue
-a.
Nucleus large and spherical; takes up most of cell
-b. T lymphocytes act directly against viral infected and
tumor cells
-c. B lymphocytes some become plasma cells which produce
antibodies
2. Monocytes
-a. Size largest of all leukocytes
-b. Macrophages once in tissue they become theses
-c. Phagocytosis of viruses and
intercellular bacteria
Leukopoiesis
1. Cytokines glycoprotein hormones stimulate production.
2. Hemocytoblast parent of all
formed elements
3. Lymphoid stem cell ultimately become lymphocytes
4. Myeloid stem cell all other formed elements
-a. Monoblast become monocytes which become macrophages
-b. Myeloblast become
granulocytes
Leukocyte disorders
1. Leukopenia abnormally low
WBC; anticancer drugs; glucocorticoids
2. Leukemia cancerous; high number unspecialized precursor
cells
3. Infectious mononucleosis Epstein-Barr virus; many
atypical granulocytes
Platelets
1. Appearance blue staining cellular fragments
2. Function hemostasis
3. Granules in platelets contain procoagulants
4. Formation
-a. megakaryoblast from myeloid
stem cell; mitosis without cytokinesis
-b. promegakaryocyte
-c. megakaryocyte
divided by cell membrane; peel off like stamps
Hemostasis
1. Vascular spasm constriction decreases blood loss
2. Platelet plug formation
-a. Collagen exposed when damaged; platelets stick to it
-b. Degranulation release
chemicals; draw platelets; clotting
3. Blood clotting
Blood clotting
1. Procoagulants promote
coagulation; made in liver and platelets
2. Calcium ion important in many stages in blood clotting
3. Two pathways to prothrombin
activator
-a. Extrinsic pathway faster; depend on factors from
tissue
-b. Intrinsic pathway slower; all procoagulants
found in blood
4. Prothrombin activator acts on
5. Prothrombin which is converted into
6. Thrombin an enzyme which acts on
7. Fibrinogen which is soluble;
converted to
8. Fibrin insoluble fibers; form mesh; catches formed
elements
9. Clot retraction contractile proteins in platelets;
compact clot
Fibrinolysis
1. Defined removal of unneeded clots
2. Plasminogen inactive enzyme;
activated by chemicals from endothelium
3. Plasmin enzyme which digest
fibrin
Disorders of hemostasis
1. Thrombus clot which occurs and persist in unbroken
blood vessel
2. Embolus clot which breaks free and floats in
bloodstream
3. Thrombocytopenia low platelets; small blood vessel
bleeding
4. Impaired liver function procoagulants
not produced; vitamin K poor absorbed
5. Hemophilia hereditary disorder; cant synthesis a procoagulant
Blood groups
1. Agglutinogen antigen found on
a RBC; glycoprotein
2. Agglutinin antibodies against agglutionogens
3. ABO blood groups agglutinins are preformed; not until 2
months old
-a. AB A and B agglutinogens; no
agglutinins
-b. A A agglutinogen; B agglutinins
-c. B B agglutinogen;
A agglutinins
-d. O no agglutinogens; A and B
agglutinins
-e. mismatched blood results in
agglutination and lysis
4. Rh blood groups agglutinins
are not preformed
-a. Rh positive Rh agglutinogen; will not form
agglutinin against
-b. Rh negative no Rh agglutinogen; will form
agglutinin against
-c. Erythroblatosis fetalis hemolytic disease of newborn; RBCs
are destroyed