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1. Water
Act as a solvent and suspending medium for blood
components
2. Ions
Involved in osmotic pressure (Na+ and Cl-)
Membrane potential (Na+ and K+)
Acid – base balance (hydrogen, hydroxide, and
bicarbonate ions)
3. Nutrients
Source of energy and “building blocks” of more
complex molecules (glucose, amino acids,
triglycerides)
Promote enzyme activity (vitamins)
4. Waste products
Breakdown products of protein metabolism (urea,
uric acids, creatinine, ammonia salts)
Breakdown products of red blood cell (bilirubin)
End product of anaerobic respiration (lactate)
5. Gases
Necessary for aerobic respiration; terminal electron Formed Elements in the Blood
acceptor in electrical – transport chain (oxygen)
1. Red Blood Cells (RBC) a. Lymphocyte
Erythrocytes - Produces antibodies and other
Most abundant in formed elements chemicals responsible for destroying
95% of the volume of the Formed elements microorganisms
Transport oxygen and carbon dioxide - Contributes to allergic reactions,
Disk – shaped; edges are thicker than center graft rejection, tumor control, and
Biconcave shape regulation of the immune system
Unable to divide - T cells (thymus) and B cells (bone
Lifespan: 120 days male – 110 days female marrow or bursa of Fabricius)
700 times more numerous than WBC - Spherical nucleus; faintly blue
17 times more numerous than platelets stained granule
2. White Blood Cells (WBC) b. Monocyte
Leukocytes Phagocytic cell in the blood
5% of the volume of the Formed elements Leaves the blood and becomes a
five types, each with specific function macrophage, which phagocytize
Granulocyte bacteria, dead cells, and other
a. Neutrophil debris within tissues
- Phagocytizes microorganisms and Largest sized WBC
other substances Kidney shaped nucleus; very faintly
- Multi – lobed nucleus; blue granules stained blue granule
b. Eosinophil 3. Platelets
- Attack certain worm parasites Thrombocytes
- Release chemical that modulates Cell fragments suspended in the blood
inflammation Forms platelet plugs
- Negatively impacts airways during Releases chemicals necessary for blood clotting
asthma attacks Minute fragments and cells consisting of a small
- Bilobed nucleus; dark pink gran amount of cytoplasm
c. Basophil
- Releases histamine, which
promotes inflammation, and
heparin, which prevents clot Production of Formed Elements
formation
- Bilobed nucleus; dark purple gran Hematopoiesis
- Hemopoiesis
Agranulocyte
Process of blood cell production
Fetus and embryo = yolk sac, liver, thymus, spleen, a. 7% dissolved in plasma
lymph nodes, red bone marrow b. 23% is combined with hemoglobin
After birth = red bone marrow c. 70% is in the form of bicarbonate ions
Hemocytoblast
e
Erythrocyt
yte
Thromboc
Neutrophil
Eosinophil
Basophil
e
Lymphocyt
Monocyte
Precursor cells capable of dividing to produce daughter
cells that can differentiate into various types of blood
cells
Divides into two cells, one undergoes differentiation and
the other stays as a hemocytoblast
ast
Hemocytobl
ast
Hemocytobl
ast
Hemocytobl
ast
Hemocytobl
ast
Hemocytobl
ast
Hemocytobl
ast
Hemocytobl
Myeloid Stem Cell and Lymphoid Stem Cell
Stem Cell
Myeloid
Stem Cell
Myeloid
Stem Cell
Myeloid
Stem Cell
Myeloid
Stem Cell
Myeloid
Stem
Myeloid
Stem Cell
Lymphoid
Red Blood Cells
last
Proerythrob
blast
Megakaryo
Myeloblast
Myeloblast
Myeloblast
Monoblast
st
Lymphobla
Transport oxygen from the lungs to the various body
tissues and to transport carbon dioxide from the tissues
to the lungs
e
Intermeidat
Early –
cyte
Megakaryo
cyte
Progranulo
cyte
Progranulo
cyte
Progranulo
Hemolysis
up
cyte break
Megakaryo
myelocyte
Neutrophilic
myelocyte
Eosinophilic
myelocyte
Basophilic
hemoglobin is release in the plasma
bland cell
Neutrophilic
band cell
Eosinophilic
band cell
Basophilic
Carbon – carrying hemoglobin
Carbon dioxide cannot bind to the hemes, instead
carbon molecules attach to the globin molecule
Carbonic anhydrase Carboxyhemoglobin
Enzyme that acts as a catalyze in the combination Stable compound resulted from the binding
of carbon dioxide and water of a carbon monoxide molecule – a poison
Converts CO2 and H2O to hydrogen ion (H+) and
produced by incomplete combustion of
bicarbonate ion (HCO3-)
gasoline that reacts strongly to the iron rings
of the hemoglobin
Inhibits the ability of hemoglobin to transport
Hemoglobin substances
Usually found in the blood of smokers
Complex protein consisting of 4 subunits
Requires iron for normal function of hemoglobin
globin = polypeptide chain bound to one heme
heme = red – pigment molecule containing one iron Life History of Erythrocytes
atom Hemocytoblasts
Embryonic
Fetal Myeloid stem cell
Adult
Proerythroblasts
Oxyhemoglobin
Early erythroblast (basophilic erythroblast)
Oxygenated form of hemoglobin
Oxygen molecules bind to each of the hemes of Because they stain with basic dye
the hemoglobin, carrying up to four molecules of Intermediate erythroblast (polychromatic erythroblast)
oxygen
Bright red They stain different colors with basic
and acidic dyes
Deoxyhemoglobin
Late erythroblast (losing of nucleus)
Hemoglobin that do not carry oxygen
Dark red Reticulocyte
Reticulum or network that can be Modified by the kidneys to give urine its
observed in the cytoplasm when a characteristic yellow color
special staining technique is used
Jaundice
Erythropoietin (EPO)
C. Chemotaxis
THREE PROCESSES OF HEMOSTASIS
- WBC can be attracted to foreign materials or dead
cells within the tissue 1. Vascular Spasm
- Immediate but temporary constriction of the blood
vessel
Pus - Occurs when smooth muscle within the wall of the
vessel contracts
Accumulation of dead WBC and bacteria, along with - Can close small vessels completely and stop the
fluid and cell debirs flow of blood through them
2. Platelet Plug Formation
- Platelet plug = accumulation of platelets that can
seal small breaks in the blood vessel
Platelets - Platelet plug is not the same as blood clotting
Glycoproteins and proteins on their surface allow - very important in maintaining the integrity of the
platelets to attach to other molecules, such as collagen Circulatory System
connective tissues
Play an important role in controlling blood loss by 1) Platelet adhesion occurs when von
a. Forming platelet plugs that seal holes in the Willebrand factor – secreted by the endothelial
blood vessels cells - connects the exposed collagen to
b. Promoting the formation and contraction of clots platelets
that help seal off larger wounds in the blood 2) Platelet release reaction – ADP,
vessel Thromboxane, and other chemicals are
released by the activated platelets by
exocytosis. These chemicals, in turn, activates - A floating thrombus
more platelets to release more chemicals and
thus creating a cascade effect. This is an
example of positive – feedback Anticoagulants
3) Platelet aggregation – occurs when fibrinogen
receptors on activated platelets bind to Antithrombin and heparin
fibrinogen, connecting the platelets together.
Clot retraction
3. Coagulation
- Blood clot – a network of threadlike proteins - Condensing of clot
called, fibrin, that traps blood cell, platelets, and - Serum in plasma is squeezed out of clot
fluid
- Formation depends on the number of proteins Fibrinolysis
formed in the plasma - Process of dissolving clot
- Plasminogen (plasma protein) breaks down clot (fibrin)
Clot Formation
1. Injury to a blood vessel causes inactive clotting to be
exposed to the connective tissue; thus, activating it
2. Thromboplastin is released causing a series of
activation of clotting factors until prothrombinase is
formed
3. Prothrombinase converts prothrombin into its active
form thrombin
4. Thrombin converts plasma protein fibrinogen to fibrin
Thrombus
- An attached clot
Embolus