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Page 1: *Lecture Outline - Damm's Science Page · 24 c. A differential white blood cell count (DIFF) can help pinpoint the nature of an illness, indicating whether it is caused by bacteria

Chapter 12 *Lecture Outline

Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

*See separate Image PowerPoint slides for all figures and tables pre-inserted into

PowerPoint without notes.

PowerPoints prepared by Melanie Waite-Altringer Biology Faculty Member of

Anoka-Ramsey Community College

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Chapter 12

Blood

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Introduction A. Blood, a type of connective tissue, is a

complex mixture of cells, chemicals, and fluid.

B. Blood transports substances throughout the body, and helps to maintain a stable internal environment.

C. The blood includes red blood cells, white blood cells, platelets, and plasma.

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D. Blood Volume and Composition 1. Plasma is a mixture of water, amino

acids, proteins, carbohydrates, lipids, vitamins, hormones, electrolytes, and cellular wastes.

2. A blood hematocrit (HCT) is normally 45% cells and 55% plasma.

3. An average-sized adult has a blood volume of about 5.3 quarts (5 liters).

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Fig12.01

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Centrifuged Blood Sample Peripheral Blood Smear

Plasma

“Buffy coat” (white blood cells and platelets) Red blood cells

Red blood cells

White blood!cells

Platelets

©Keith Brofsky/Getty Images ©Keith Brofsky/Getty Images ©Comstock/Punchstock

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Blood Cells A. Red Blood Cells

1. Red blood cells (erythrocytes) are biconcave disks that contain one-third oxygen-carrying hemoglobin by volume.

2. When oxygen combines with hemoglobin bright red oxyhemoglobin results.

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3. Deoxygenated blood (deoxyhemoglobin) is darker.

4 Red blood cells discard their nuclei during development and so cannot reproduce or produce proteins.

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B. Red Blood Cell Counts 1. The typical red blood cell count is

4,600,000-6,2000,000 cells per mm3 for males and 4,200,000-5,400,000 cells per mm3 for females.

2. The number of red blood cells is a measure of the blood's oxygen-carrying capacity.

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C. Red Blood Cell Production and Its Control 1. In the embryo and fetus, red blood cell production occurs in the yolk sac, liver, and spleen; after birth, it occurs in the red bone marrow.

2. The average life span of a red blood cell is 120 days.

3. The stages of red blood cell formation from hematopoietic stem cells (hemocytoblasts) is diplayed in Figure 12.4

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Fig12.04a

Megakaryoblast

Myeloid stem cell Lymphoid stem cell!

Megakaryocyte

Thrombocytes!(platelets) Monocyte

Macrophage

T lymphocyte! B lymphocyte

Plasma cell

Myeloblast

Progranulocyte

Erythroblast

Normoblast

Reticulocyte

Erythrocyte

Neutrophilic!band cell Basophilic!

band cel Eosinophilic!band cell

Neutrophil Basophil Granulocytes

Eosinophil

Neutrophilic!myelocyte Basophilic!

myelocyte Eosinophilic!myelocyte

Proerythroblast Monoblast

Promonocyte Prolymphocyte Prolymphocyte

Lymphoblast!T cell!

precursor Lymphoblast!

B cell!precursor

Agranulocytes

(a)

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In re

d bo

ne m

arro

w

In c

ircul

atin

g bl

ood

Activ

ated

in ti

ssue

s!(s

ome

cells

)

Hematopoietic stem cell

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4. The total number of red blood cells remains relatively constant due to a negative feedback mechanism utilizing the hormone erythropoietin, which is released from the kidneys and liver in response to the detection of low oxygen levels.

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D. Dietary Factors Affecting Red Blood Cell Production

1. Vitamins B12 and folic acid are needed for DNA synthesis, so they are necessary for the reproduction of all body cells, especially in

hematopoietic tissue.

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2. Iron is needed for hemoglobin synthesis.

3. A deficiency in red blood cells or quantity of hemoglobin results in anemia.

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E. Destruction of Red Blood Cells 1. With age, red blood cells become

increasingly fragile and are damaged by passing through narrow capillaries.

2. Macrophages in the liver and spleen phagocytize damaged red blood cells.

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3. Hemoglobin from the decomposed red blood cells is converted into heme and globin.

4. Heme is decomposed into iron which is stored or recycled and biliverdin and bilirubin which are excreted in bile.

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F. White Blood Cells 1. White blood cells (leukocytes) help

defend the body against disease. 2. They are formed from hemocytoblasts

(hematopoietic stem cells). 3. Hormones that stimulate WBC production fall into two categories,

interleukins and colony-stimulating factors (CSF’s).

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3. Five types of white blood cells are in circulating blood and are distinguished by size, granular appearance of the cytoplasm, shape of the nucleus, and staining characteristics.

4. The types of white blood cells are the granulocytes, neutrophils, eosinophils, and basophils, and the agranulocytes monocytes and lymphocytes.

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a. Neutrophils have red-staining fine cytoplasmic granules and a multi-lobed nucleus; they comprise 54-62% of leukocytes.

b. Eosinophils have coarse granules that stain deep red, a bilobed nucleus, and make up only 1-3% of circulating leukocytes.

c. Basophils have fewer granules that stain blue; they account for fewer than 1% of leukocytes.

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d. Monocytes are the largest blood cells, have variably-shaped nuclei, and make up 3-9% of circulating leukocytes.

e. Lymphocytes are long-lived, have a large, round nucleus, and account for 25-33% of circulating leukocytes.

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4. Functions of White Blood Cells a. Leukocytes can squeeze between

cells lining walls of blood vessels by diapedesis and attack bacteria and debris.

b. Neutrophils and monocytes are phagocytic, with monocytes engulfing the larger particles. Both of these contain many lysosomes that help

breakdown organic molecules.

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Fig12.02

(54–62%) (1–3%) (<1%) (3–9%) (25–33%)

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Blood

Plasma Formed elements

Platelets Red blood cells White blood cells Electrolytes Water Proteins Wastes Nutrients Gases Vitamins

Hormones

Neutrophils Eosinophils Basophils Monocytes Lymphocytes Albumins Globulins Fibrinogen N2 O2 CO2

(4.8%) (95.1%) (0.1%) (92%) ( 7%)

45% 55%

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c. Eosinophils moderate allergic reactions as well as defend against parasitic infections.

d. Basophils migrate to damaged tissues and release histamine to promote inflammation and heparin

to inhibit blood clotting. e. Lymphocytes are the major

players in specific immune reactions and some produce antibodies.

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5. White Blood Cell Counts a. Normally a cubic milliliter of blood contains 4,000 to 11,000

white blood cells. b. Leukocytosis occurs after an

infection when excess numbers of leukocytes are present; leukopenia occurs from a variety of conditions, including AIDS.

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c. A differential white blood cell count (DIFF) can help pinpoint the nature of an illness, indicating whether it is caused by bacteria or viruses.

i. A differential white blood cell count lists the percentages of the types of leukocytes in a blood sample.

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G. Blood Platelets 1. Blood platelets or thrombocytes are

fragments of megakaryocytes, developed from hematopoietic stem cells in response to thrombopoietin.

2. Platelets help repair damaged blood vessels by adhering to their broken edges.

3. Normal platelet counts vary from 130,000 to 360,000 platelets per mm3.

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Blood Plasma A. Plasma is the clear, straw-colored fluid portion

of the blood. 1. Plasma is mostly water (92%) but

contains a variety of substances. 2. Plasma functions to transport nutrients

and gases, regulate fluid and electrolyte balance, and maintain a favorable pH.

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B. Plasma Proteins 1. The plasma proteins are the most

abundant dissolved substances in the plasma.

2. Plasma proteins are not used for energy and fall into three groups-albumins, globulins, and fibrinogen.

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a. The albumins help maintain the osmotic pressure of the blood and account for 60% of the plasma proteins.

b. The globulins, comprising 36% of the plasma proteins, are designated

as alpha, beta, and gamma globulins.

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i. Alpha and beta globulins function in transporting lipids and fat-soluble vitamins.

ii. Gamma globulins are a type of antibody.

c. Fibrinogen (4%) plays a primary role in blood coagulation.

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C. Gases and Nutrients 1. The most important blood gases are

oxygen and carbon dioxide. 2. The plasma nutrients include amino

acids, monosaccharides, nucleotides, and lipids.

3. Since lipids are not soluble in the water of the plasma, they are surrounded by protein molecules for

transport through the bloodstream as lipoproteins.

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D. Nonprotein Nitrogenous Substances 1. Nonprotein nitrogenous substances

generally include amino acids, urea, and uric acid, creatine and creatinine.

a. Urea and uric acid are the by- products of protein and nucleic acid catabolism.

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E. Plasma Electrolytes 1. Plasma electrolytes are absorbed by the

intestine or are by-products of cellular metabolism.

2. They include sodium, potassium, calcium, magnesium, chloride, bicarbonate, phosphate, and sulfate ions.

3. Some of these ions are important in maintaining osmotic pressure and pH of the plasma.

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Hemostasis A. Hemostasis refers to the stoppage of bleeding.

1. Following injury to a vessel, three steps occur in hemostasis: blood vessel spasm, platelet plug formation, and blood coagulation.

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B. Blood Vessel Spasm 1. Cutting a blood vessel causes the

muscle in its walls to contract in a reflex, or engage in vasospasm.

2. This reflex lasts only a few minutes, but it lasts long enough (30 minutes) to initiate the second and third steps of hemostasis.

3. Platelets release serotonin at this time constricting smooth muscles in the blood vessel walls.

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C. Platelet Plug Formation 1. Platelets stick to the exposed edges of

damaged blood vessels, forming a net with spiny processes protruding from their membranes.

2. A platelet plug is most effective on a small vessel.

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D. Blood Coagulation 1. Blood coagulation is the most effective

means of hemostasis. 2. Blood coagulation is very complex and

uses clotting factors. 3. Damaged tissues release a chemical

called tissue thromboplastin, which activates the first in a series of factors leading to the production of prothrombin activator.

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4. Prothrombin activator converts prothrombin in the plasma into thrombin. This in turn, catalyzes a reaction that converts

fibrinogen into fibrin. 5. The major event in blood clot formation

is the conversion of soluble fibrinogen into net like insoluble fibrin causing the blood cells to catch.

6. Serum is plasma minus the clotting factors. 7. The amount of prothrombin activator

formed is proportional to the amount of tissue damage.

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8. Once a blood clot forms, it promotes still more clotting through a positive feedback system.

9. After a clot forms, fibroblasts invade the area and produce fibers throughout the

clots. 10. A clot that forms abnormally in a vessel

is a thrombus; if it dislodges, it is an embolus.

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Fig12.16

Tissue damage

Blood vessel!spasm

Platelet plug!formation

Clotting!mechanism

Prothrombin!activator!

Prothrombin

Ca+2!

Ca+2!Thrombin

Fibrinogen

Fibrin

Blood clot!formation!

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Blood Groups and Transfusions A. After mixed success with transfusions,

scientists determined that blood was of different types and only certain combinations were compatible.

B. Antigens and Antibodies 1. Clumping of red blood cells following

transfusion is called agglutination.

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2. Agglutination is due to the interaction of proteins on the surfaces of red blood cells (antigens) with certain antibodies carried in the plasma.

3. Only a few of the antigens on red blood cells produce transfusion reactions.

a. These include the ABO group and Rh group.

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C. ABO Blood Group 1. Type A blood has A antigens on red

blood cells and anti-B antibodies in the plasma.

2. Type B blood has B antigens on red blood cells and anti-A antibodies in the plasma.

3. Type AB blood has both A and B antigens, but no antibodies in the plasma.

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4. Type O blood has neither antigen, but both types of antibodies in the plasma.

5. Adverse transfusion reactions are avoided by preventing the mixing of blood that contains matching antigens and antibodies.

a. Adverse reactions are due to the agglutination of red blood cells.

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D. Rh Blood Group 1. The Rh blood group was named after

the rhesus monkey. 2. If the Rh factor surface protein is

present on red blood cells, the blood is Rh positive; otherwise it is Rh negative.

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3. There are no corresponding antibodies in the plasma unless a person with Rh- negative blood is transfused with Rh- positive blood; the person will then develop antibodies for the Rh factor.

4. Erythroblastosis fetalis develops in Rh- positive fetuses of Rh-negative mothers but can now be prevented.

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