Blood: Lecture Presentation by Patty Bostwick-Taylor Florence-Darlington Technical College

Chapter 10
Blood
Lecture Presentation by
Patty Bostwick-Taylor
Florence-Darlington Technical College
© 2018 Pearson Education, Ltd.

Blood
 Blood transports everything that must be carried

from one place to another, such as:
 Nutrients
 Wastes
 Hormones
 Body heat

Components of Blood
 Blood is the only fluid tissue, a type of connective

tissue, in the human body
 Components of blood
 Formed elements
 Plasma

Components of Blood
 When blood is separated:

 Erythrocytes sink to the bottom (45 percent of blood, a
percentage known as the hematocrit)
 Buffy coat contains leukocytes and platelets (less than
1 percent of blood)
 Buffy coat is a thin, whitish layer between the
erythrocytes and plasma
 Plasma rises to the top (55 percent of blood)

Figure 10.1 The composition of blood.
Plasma 55%
Constituent Major Functions Formed elements (cells) 45%
Water 90% of plasma Number

Cell Type Functions
volume; solvent (per mm3 of blood)
for carrying other
substances; Erythrocytes
absorbs heat (red blood cells)
4–6 million Transport oxygen
and help transport
Salts (electrolytes) carbon dioxide
Sodium Osmotic balance,
Potassium pH buffering,
Leukocytes
Calcium regulation of 4,800–10,800 Defense and
(white blood cells)
Magnesium membrane immunity
Chloride permeability
Bicarbonate
Lymphocyte
Plasma proteins Basophil
Albumin Osmotic balance,
pH buffering
Clotting of blood Eosinophil
Fibrinogen
Globulins Defense (antibodies)
and lipid transport Neutrophil Monocyte
Substances transported by blood Platelets
Nutrients (glucose, fatty acids, amino 250,000–400,000 Blood clotting
acids, vitamins)
Waste products of metabolism
(urea, uric acid)
Respiratory gases (O2 and CO2)
Hormones (steroids and thyroid hormone
are carried by plasma proteins)
Physical Characteristics and Volume
 Blood characteristics
 Sticky, opaque fluid
 Heavier and thicker than water
 Color range
 Oxygen-rich blood is scarlet red
 Oxygen-poor blood is dull red or purple
 Metallic, salty taste
 Blood pH is slightly alkaline, between 7.35 and 7.45
 Blood temperature is slightly higher than body
temperature, at 38ºC or 100.4ºF

Physical Characteristics and Volume
 Blood volume
 About 5–6 liters, or about 6 quarts, of blood are found
in a healthy adult
 Blood makes up 8 percent of body weight

Plasma
 90 percent water
 Straw-colored fluid
 Includes many dissolved substances
 Nutrients
 Salts (electrolytes)
 Respiratory gases
 Hormones
 Plasma proteins
 Waste products

Plasma
 Plasma proteins
 Most abundant solutes in plasma
 Most are made by the liver
 Include:
 Albumin—an important blood buffer and contributes to
osmotic pressure
 Clotting proteins—help to stem blood loss when a blood
vessel is injured
 Antibodies—help protect the body from pathogens

Plasma
 Blood composition varies as cells exchange

substances with the blood
 Liver makes more proteins when levels drop
 Respiratory and urinary systems restore blood pH to
normal when blood becomes too acidic or alkaline
 Plasma helps distribute body heat

Formed Elements
 Erythrocytes
 Red blood cells (RBCs)
 Leukocytes
 White blood cells (WBCs)
 Platelets
 Cell fragments

Figure 10.2 Photomicrograph of a blood smear.
Lymphocyte Platelets
Erythrocytes Neutrophils
Formed Elements
 Erythrocytes (red blood cells, or RBCs)

 Main function is to carry oxygen
 RBCs differ from other blood cells
 Anucleate (no nucleus)
 Contain few organelles; lack mitochondria
 Essentially bags of hemoglobin (Hb)
 Shaped like biconcave discs
 Normal count is 5 million RBCs per cubic millimeter
(mm3) of blood

Formed Elements
 Erythrocytes (continued)
 Hemoglobin is an iron-bearing protein
 Binds oxygen
 Each hemoglobin molecule can bind 4 oxygen
molecules
 Each erythrocyte has 250 million hemoglobin molecules
 Normal blood contains 12–18 g of hemoglobin per
100 milliliters (ml) of blood

Formed Elements
 Homeostatic imbalance of RBCs

 Anemia is a decrease in the oxygen-carrying ability of
the blood due to:
 Lower-than-normal number of RBCs
 Abnormal or deficient hemoglobin content in the RBCs
 Sickle cell anemia (SCA) results from abnormally
shaped hemoglobin

Homeostatic Imbalance 10.1 Comparison of (a) a normal erythrocyte to (b) a sickled erythrocyte (6,550×).
2 3 7...146 2 3 7...146
1 1
4 6 4 6
5 5
(a) Normal RBC and part of the (b) Sickled RBC and part of its
amino acid sequence of its hemoglobin sequence
hemoglobin

Formed Elements
 Polycythemia
 Disorder resulting from excessive or abnormal
increase of RBCs due to:
 Bone marrow cancer (polycythemia vera)
 Life at higher altitudes (secondary polycythemia)
 Increase in RBCs slows blood flow and increases
blood viscosity

Table 10.1 Types of Anemia

Formed Elements
 Leukocytes (white blood cells, or WBCs)

 Crucial in body’s defense against disease
 Complete cells, with nucleus and organelles
 Able to move into and out of blood vessels
 Respond to chemicals released by damaged tissues
(known as positive chemotaxis)
 Move by amoeboid motion
 4,800 to 10,800 WBCs per mm3 of blood

Formed Elements
 Leukocytosis
 WBC count above 11,000 cells per mm3 of blood
 Generally indicates an infection
 Leukopenia
 Abnormally low WBC count
 Commonly caused by certain drugs, such as
corticosteroids and anticancer agents
 Leukemia
 Bone marrow becomes cancerous
 Numerous immature WBC are produced

Formed Elements
 Types of leukocytes
 Granulocytes
 Granules in their cytoplasm can be stained
 Possess lobed nuclei
 Include neutrophils, eosinophils, and basophils
 Agranulocytes
 Lack visible cytoplasmic granules
 Nuclei are spherical, oval, or kidney-shaped
 Include lymphocytes and monocytes

Formed Elements
 List of the WBCs, from  Easy way to remember

most to least abundant this list
 Neutrophils  Never
 Lymphocytes  Let
 Monocytes  Monkeys
 Eosinophils  Eat
 Basophils  Bananas

Formed Elements
 Granulocytes
 Neutrophils
 Multilobed nucleus
 Cytoplasm stains pink and contains fine granules
 Function as phagocytes at active sites of infection
 Numbers increase during infection
 3,000–7,000 neutrophils per mm3 of blood (40–70 percent
of WBCs)

Formed Elements
 Granulocytes (continued)
 Eosinophils
 Nucleus stains blue-red
 Brick-red cytoplasmic granules
 Function is to kill parasitic worms and play a role in
allergy attacks
 100–400 eosinophils per mm3 of blood (1–4 percent of
WBCs)

Formed Elements
 Granulocytes (continued)
 Basophils
 Rarest of the WBCs
 Large granules that stain dark blue
 Contain heparin (anticoagulant)
 20–50 basophils per mm3 of blood (0–1 percent of
WBCs)

Formed Elements
 Agranulocytes
 Lymphocytes
 Large, dark purple nucleus
 Slightly larger than RBCs
 Reside in lymphatic tissues
 Play a role in immune response
 1,500–3,000 lymphocytes per mm3 of blood (20–45 percent
of WBCs)

Formed Elements
 Agranulocytes (continued)
 Monocytes
 Largest of the white blood cells
 Distinctive U- or kidney-shaped nucleus
 Function as macrophages when they migrate into
tissues
 Important in fighting chronic infection
 100–700 monocytes per mm3 of blood (4–8 percent of
WBCs)

Formed Elements
 Platelets
 Fragments of multinucleate cells
 Needed for the clotting process
 Normal platelet count is 300,000 platelets per mm3 of
blood

Table 10.2 Characteristics of Formed Elements of the Blood (1 of 3)



Hematopoiesis (Blood Cell Formation)
 Hematopoiesis is the process of blood cell

formation
 Occurs in red bone marrow (myeloid tissue)
 All blood cells are derived from a common stem
cell (hemocytoblast)
 Hemocytoblasts form two types of descendants
 Lymphoid stem cell, which produces lymphocytes
 Myeloid stem cell, which can produce all other formed
elements

Figure 10.3 The development of blood cells.
Hemocytoblast
stem cells
Lymphoid Myeloid
stem cells stem cells
Secondary stem cells
Basophils
Erythrocytes
Platelets
Eosinophils
Lymphocytes Monocytes Neutrophils

Formation of Red Blood Cells
 Since RBCs are anucleate, they are unable to

divide, grow, or synthesize proteins
 RBCs wear out in 100 to 120 days
 When worn out, RBCs are eliminated by
phagocytes in the spleen or liver
 Lost cells are replaced by division of
hemocytoblasts in the red bone marrow

Formation of Red Blood Cells
 Rate of RBC production is controlled by a

hormone
 Kidneys produce most erythropoietin as a
response to reduced oxygen levels in the blood
 Homeostasis is maintained by negative feedback
from blood oxygen levels

Figure 10.4 Mechanism for regulating the rate of RBC production. Slide 1
IMB
AL
AN
CE
Homeostasis: Normal blood oxygen levels
1 Stimulus
5 O2–carrying IMB Low blood O2–carrying ability
AL due to
ability of blood AN
CE • Decreased RBC count
increases.
• Decreased amount of
hemoglobin
• Decreased availability of O2
4 Enhanced
erythropoiesis
2 Kidneys (and liver,
increases RBC
to a smaller extent)
count.
release erythropoietin.
3 Erythropoietin
stimulates red bone
marrow.

IMB
AL
AN
CE
1 Stimulus
IMB Low blood O2–carrying ability
AL due to
AN
hemoglobin

IMB
AL
AN
CE
1 Stimulus
AL due to
AN
hemoglobin


IMB
AL
AN
CE
1 Stimulus
AL due to
AN
hemoglobin

3 Erythropoietin
stimulates red bone
marrow.

IMB
AL
AN
CE
1 Stimulus
AL due to
AN
hemoglobin
4 Enhanced
erythropoiesis
increases RBC
count.
3 Erythropoietin
stimulates red bone
marrow.

IMB
AL
AN
CE
1 Stimulus
5 O2–carrying IMB Low blood O2–carrying ability
AL due to
ability of blood AN
increases.
hemoglobin
4 Enhanced
erythropoiesis
increases RBC
count.
3 Erythropoietin
stimulates red bone
marrow.

Formation of White Blood Cells and
Platelets
 WBC and platelet production is controlled by
hormones
 Colony stimulating factors (CSFs) prompt bone
marrow to generate leukocytes
 Thrombopoietin stimulates production of platelets from
megakaryocytes

Hemostasis
 Hemostasis is the process of stopping the

bleeding that results from a break in a blood
vessel
 Hemostasis involves three phases
1. Vascular spasms
2. Platelet plug formation
3. Coagulation (blood clotting)

Hemostasis
 Step 1: vascular spasms

 Immediate response to blood vessel injury
 Vasoconstriction causes blood vessel to spasm
 Spasms narrow the blood vessel, decreasing blood
loss

Figure 10.5 Events of hemostasis. Slide 2
Step 1 Vascular spasms occur.
• Smooth muscle contracts,

causing vasoconstriction.

Hemostasis
 Step 2: platelet plug formation

 Collagen fibers are exposed by a break in a blood
vessel
 Platelets become “sticky” and cling to fibers
 Anchored platelets release chemicals to attract more
platelets
 Platelets pile up to form a platelet plug (white
thrombus)

Step 2 Platelet plug forms.

• Injury to lining of vessel exposes
collagen fibers; platelets adhere.
Collagen
fibers
• Platelets release chemicals that
make nearby platelets sticky;
platelet plug forms.
Platelets

Hemostasis
 Step 3: coagulation
 Injured tissues release tissue factor (TF)
 PF3 (a phospholipid) interacts with TF, blood protein
clotting factors, and calcium ions to trigger a clotting
cascade
 Prothrombin activator converts prothrombin to
thrombin

Hemostasis
 Step 3: coagulation (continued)

 Thrombin joins fibrinogen proteins insoluble fibrin
 Fibrin forms a meshwork
 Within the hour, serum is squeezed from the clot as it
retracts
 Serum is plasma minus clotting proteins

Step 3 Coagulation events occur.

• Clotting factors present in plasma
and released by injured tissue cells
interact with Ca2+ to form thrombin,
the enzyme that catalyzes joining of
Fibrin fibrinogen molecules in plasma to fibrin.
• Fibrin forms a mesh that traps red blood

cells and platelets, forming the clot.

Figure 10.6 Fibrin clot.

Hemostasis
 Blood usually clots within 3 to 6 minutes

 The clot remains as endothelium regenerates
 The clot is broken down after tissue repair

Disorders of Hemostasis
 Undesirable clotting
 Thrombus
 A clot in an unbroken blood vessel
 Can be deadly in areas such as the lungs
 Embolus
 A thrombus that breaks away and floats freely in the
bloodstream
 Can later clog vessels in critical areas such as the brain

 Bleeding disorders
 Thrombocytopenia
 Insufficient number of circulating platelets
 Arises from any condition that suppresses the bone
marrow
 Even normal movements can cause bleeding from small
blood vessels that require platelets for clotting
 Evidenced by petechiae (small purplish blotches on the
skin)

 Bleeding disorders (continued)

 Hemophilia
 Hereditary bleeding disorder
 Normal clotting factors are missing
 Minor tissue damage can cause life-threatening
prolonged bleeding

Blood Groups and Transfusions
 Large losses of blood have serious

consequences
 Loss of 15 to 30 percent causes weakness
 Loss of over 30 percent causes shock, which can be
fatal
 Blood transfusions are given for substantial blood
loss, to treat severe anemia, or for
thrombocytopenia

Human Blood Groups
 Blood contains genetically determined proteins

known as antigens
 Antigens are substances that the body recognizes
as foreign and that the immune system may attack
 Most antigens are foreign proteins
 We tolerate our own “self” antigens
 Antibodies are the “recognizers” that bind foreign
antigens
 Blood is “typed” by using antibodies that will cause
blood with certain proteins to clump and lyse

Human Blood Groups
 There are over 30 common red blood cell

antigens
 The most vigorous transfusion reactions are
caused by ABO and Rh blood group antigens

Human Blood Groups
 ABO blood group

 Blood types are based on the presence or absence of
two antigens
1. Type A
2. Type B

Human Blood Groups
 ABO blood group (continued)

 Presence of both antigens A and B is called type AB
 Presence of antigen A is called type A
 Presence of antigen B is called type B
 Lack of both antigens A and B is called type O

Human Blood Groups
 ABO blood group (continued)

 Type AB can receive A, B, AB, and O blood
 Type AB is the “universal recipient”
 Type B can receive B and O blood
 Type A can receive A and O blood
 Type O can receive O blood
 Type O is the “universal donor”

Table 10.3 ABO Blood Groups (1 of 2)

Table 10.3 ABO Blood Groups (2 of 2)

Human Blood Groups
 Rh blood group
 Named for the eight Rh antigens (agglutinogen D)
 Most Americans are Rh+ (Rh-positive), meaning they
carry the Rh antigen
 If an Rh–(Rh-negative) person receives Rh+ blood:
 The immune system becomes sensitized and begins
producing antibodies; hemolysis does not occur,
because as it takes time to produce antibodies
 Second, and subsequent, transfusions involve
antibodies attacking donor’s Rh+ RBCs, and hemolysis
occurs (rupture of RBCs)

Human Blood Groups
 Rh-related problem during pregnancy

 Danger occurs only when the mother is Rh–, the father
is Rh+, and the child inherits the Rh+ factor
 RhoGAM shot can prevent buildup of anti-Rh+
antibodies in mother’s blood

Human Blood Groups
 The mismatch of an Rh– mother carrying an Rh+

baby can cause problems for the unborn child
 The first pregnancy usually proceeds without
problems; the immune system is sensitized after the
first pregnancy
 In a second pregnancy, the mother’s immune system
produces antibodies to attack the Rh+ blood

Blood Typing
 Blood samples are mixed with anti-A and anti-B

serum
 Agglutination or the lack of agglutination leads to
identification of blood type
 Typing for ABO and Rh factors is done in the
same manner
 Cross matching—testing for agglutination of
donor RBCs by the recipient’s serum, and vice
versa

Figure 10.7 Blood typing of ABO blood groups.
Blood being tested Serum

Anti-A Anti-B
Type AB
(contains antigens A and B;
agglutinates with both sera)
Agglutinated
RBCs
Type B
(contains antigen B;
agglutinates with
anti-B serum)
Type A
(contains antigen A;
agglutinates with
anti-A serum)
Type O
(contains no antigens;
does not agglutinate with
either serum)

Developmental Aspects of Blood
 Sites of blood cell formation

 The fetal liver and spleen are early sites of blood cell
formation
 Bone marrow takes over hematopoiesis by the
seventh month

 Congenital blood defects include various types of

hemolytic anemias and hemophilia
 Incompatibility between maternal and fetal blood
can result in fetal cyanosis, resulting from
destruction of fetal blood cells
 Fetal hemoglobin differs from hemoglobin
produced after birth
 Physiologic jaundice occurs in infants when the
liver cannot rid the body of hemoglobin
breakdown products fast enough

 Leukemias are most common in the very young

and very old
 Older adults are also at risk for anemia and clotting
disorders

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Chapter 10

© 2018 Pearson Education, Ltd.

 Blood transports everything that must be carried

© 2018 Pearson Education, Ltd.

 Blood is the only fluid tissue, a type of connective

© 2018 Pearson Education, Ltd.

 When blood is separated:

© 2018 Pearson Education, Ltd.

Constituent Major Functions Formed elements (cells) 45%

Water 90% of plasma Number

© 2018 Pearson Education, Ltd.

© 2018 Pearson Education, Ltd.

© 2018 Pearson Education, Ltd.

© 2018 Pearson Education, Ltd.

 Blood composition varies as cells exchange

© 2018 Pearson Education, Ltd.

© 2018 Pearson Education, Ltd.

 Erythrocytes (red blood cells, or RBCs)

© 2018 Pearson Education, Ltd.

© 2018 Pearson Education, Ltd.

 Homeostatic imbalance of RBCs

© 2018 Pearson Education, Ltd.

© 2018 Pearson Education, Ltd.

© 2018 Pearson Education, Ltd.

© 2018 Pearson Education, Ltd.

 Leukocytes (white blood cells, or WBCs)

© 2018 Pearson Education, Ltd.

© 2018 Pearson Education, Ltd.

© 2018 Pearson Education, Ltd.

 List of the WBCs, from  Easy way to remember

© 2018 Pearson Education, Ltd.

© 2018 Pearson Education, Ltd.

© 2018 Pearson Education, Ltd.

© 2018 Pearson Education, Ltd.

© 2018 Pearson Education, Ltd.

© 2018 Pearson Education, Ltd.

© 2018 Pearson Education, Ltd.

© 2018 Pearson Education, Ltd.

© 2018 Pearson Education, Ltd.

© 2018 Pearson Education, Ltd.

 Hematopoiesis is the process of blood cell

© 2018 Pearson Education, Ltd.

Secondary stem cells

Lymphocytes Monocytes Neutrophils

© 2018 Pearson Education, Ltd.

 Since RBCs are anucleate, they are unable to

© 2018 Pearson Education, Ltd.

 Rate of RBC production is controlled by a

© 2018 Pearson Education, Ltd.

© 2018 Pearson Education, Ltd.

© 2018 Pearson Education, Ltd.

2 Kidneys (and liver,

© 2018 Pearson Education, Ltd.

2 Kidneys (and liver,

© 2018 Pearson Education, Ltd.

© 2018 Pearson Education, Ltd.

© 2018 Pearson Education, Ltd.

© 2018 Pearson Education, Ltd.

 Hemostasis is the process of stopping the