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Chapter 10 – Blood: Composition, Functions, and Clinical Aspects

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Blood: Composition and Functions

Overview of Blood

Blood is the only fluid tissue in the human body and is classified as a connective tissue. It consists of living cells, known as formed elements, suspended in a non-living matrix called plasma. Blood plays a critical role in transport, regulation, and protection within the body.

  • Volume: 5–6 liters in a healthy adult male (about 8% of body weight)

  • pH: Maintained between 7.35–7.45

  • Color: Scarlet red when oxygen-rich, dull red when oxygen-poor

Components of Blood

  • Formed Elements: Erythrocytes (RBCs), Leukocytes (WBCs), Platelets

  • Plasma: 90% water, contains nutrients, electrolytes, respiratory gases, hormones, plasma proteins, and waste products

Plasma Proteins: Albumin (regulates osmotic pressure), clotting proteins, and antibodies.

Formed Elements of Blood

Main Types and Functions

The formed elements of blood include erythrocytes, leukocytes, and platelets, each with distinct functions essential for homeostasis.

  • Erythrocytes (Red Blood Cells): Transport oxygen and help transport carbon dioxide

  • Leukocytes (White Blood Cells): Defense and immunity

  • Platelets: Blood clotting

Table of formed elements: cell types, numbers, and functions

Blood Smear and Cell Identification

A blood smear under the microscope reveals the various formed elements, including erythrocytes, leukocytes (such as lymphocytes and neutrophils), and platelets. This visualization aids in the identification and study of blood cell morphology.

Photomicrograph of a blood smear with labeled cell types

Characteristics of Formed Elements

Each formed element has unique anatomical and functional characteristics. Leukocytes are further divided into granulocytes and agranulocytes, with specific roles in immune defense. Platelets are essential for hemostasis.

Cell Type

Occurrence in Blood (per mm3)

Cell Anatomy

Function

Lymphocytes

1500–3000 (20–45% of WBCs)

Pale blue cytoplasm, large dark purple-blue nucleus

Part of immune system; B lymphocytes produce antibodies, T lymphocytes involved in graft rejection, fighting tumors and viruses

Monocytes

100–700 (4–8% of WBCs)

Abundant gray-blue cytoplasm, dark blue-purple nucleus (kidney-shaped)

Phagocytosis; important in fighting chronic infection

Platelets

150,000–500,000

Irregularly shaped cell fragments, stain deep purple

Needed for normal blood clotting; help control blood loss from broken vessels

Table of characteristics of formed elements of the blood

Erythrocytes and Hemoglobin

Structure and Function

Erythrocytes are biconcave, anucleate cells specialized for oxygen transport. They are essentially sacs of hemoglobin, an iron-containing protein that binds oxygen reversibly. Each erythrocyte contains about 250 million hemoglobin molecules, and normal blood contains 12–18 g of hemoglobin per 100 mL.

Homeostatic Imbalances: Anemia and Polycythemia

Anemia is a condition characterized by a decreased oxygen-carrying capacity of the blood. It can result from a reduction in RBC number, inadequate hemoglobin content, or abnormal hemoglobin. Polycythemia is an abnormal increase in RBCs.

Direct Cause

Resulting From

Leading To

Decrease in RBC number

Sudden hemorrhage, lysis of RBCs, lack of vitamin B12, depression/destruction of bone marrow

Hemorrhagic anemia, hemolytic anemia, pernicious anemia, aplastic anemia

Inadequate hemoglobin content in RBCs

Lack of iron or slow/prolonged bleeding

Iron deficiency anemia

Abnormal hemoglobin in RBCs

Genetic defect (e.g., sickle cell anemia)

Sickle cell anemia

Table of types of anemia: causes and outcomes

Sickle Cell Anemia vs. Normal Hemoglobin

Sickle cell anemia is caused by a genetic mutation resulting in abnormal hemoglobin, which distorts RBC shape under low oxygen conditions. This leads to impaired oxygen delivery and increased risk of vessel blockage.

  • Normal Hemoglobin: Glutamic acid at position 6 of the beta chain

  • Sickle Cell Hemoglobin: Valine replaces glutamic acid at position 6

Sickled erythrocyte and hemoglobin sequence Normal erythrocyte and hemoglobin sequence

Blood Groups and Transfusions

ABO Blood Groups

Blood groups are determined by the presence or absence of antigens (A and B) on the surface of erythrocytes. Antibodies are produced against antigens not present in the individual's own blood. Compatibility is crucial for safe transfusions to avoid agglutination.

Blood Group

Frequency (% U.S. population)

RBC Antigens

Plasma Antibodies

Blood that can be received

AB

4 (White), 4 (Black), 5 (Asian), <1 (Native American)

A, B

None

A, B, AB, O (Universal recipient)

B

11, 20, 27, 4

B

Anti-A

B, O

A

40, 27, 26, 16

A

Anti-B

A, O

O

45, 49, 40, 79

None

Anti-A, Anti-B

O (Universal donor)

Table of ABO blood groups, antigens, antibodies, and compatibility

Blood Typing and Agglutination

Blood typing involves mixing blood samples with anti-A and anti-B sera. Agglutination indicates the presence of the corresponding antigen. This process is essential for determining compatibility before transfusions.

Blood typing: agglutination reactions with anti-A and anti-B sera

Rh Blood Groups and Clinical Significance

The Rh system is based on the presence or absence of the Rh antigen (D antigen). Most individuals are Rh positive. Problems can arise when Rh– individuals are exposed to Rh+ blood, especially during pregnancy, leading to hemolytic disease of the newborn. Preventive treatment with RhoGAM can inhibit antibody formation.

  • Rh+: Presence of D antigen

  • Rh–: Absence of D antigen

  • Clinical Note: Rh incompatibility is a concern in Rh– mothers carrying Rh+ fetuses, especially in subsequent pregnancies.

Summary Table: Key Blood Concepts

Component

Main Function

Clinical Relevance

Erythrocytes

Oxygen transport

Anemia, polycythemia, sickle cell disease

Leukocytes

Immunity

Leukocytosis, leukopenia, leukemia

Platelets

Clotting

Thrombocytopenia, bleeding disorders

Plasma

Transport of solutes

Edema, clotting disorders

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