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Chapter 17: Blood – Structure, Function, and Clinical Relevance

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Blood: Overview and Functions

Introduction to Blood

Blood is a specialized connective tissue that plays a critical role in the transport of substances, regulation of physiological parameters, and protection against disease. It is the only fluid tissue in the human body and is essential for maintaining homeostasis.

  • Transport: Delivers oxygen and nutrients, removes metabolic wastes, and transports hormones.

  • Regulation: Maintains body temperature, pH balance, and fluid volume.

  • Protection: Prevents blood loss through clotting and combats infection via immune cells and proteins.

Composition of Blood

Major Components

Blood consists of a liquid matrix called plasma and formed elements (cells and cell fragments) suspended within it. When centrifuged, blood separates into three layers:

  • Plasma: ~55% of whole blood; the least dense component.

  • Buffy coat: <1% of blood; contains leukocytes (white blood cells) and platelets.

  • Erythrocytes: ~45% of blood (hematocrit); the most dense component.

Major components of whole blood after centrifugation

Blood Plasma

Plasma is a straw-colored, sticky fluid that makes up about 90% water and contains over 100 dissolved solutes, including nutrients, gases, hormones, wastes, proteins, and inorganic ions. Plasma proteins, mainly produced by the liver, are the most abundant solutes and serve various functions such as transport, buffering, and maintaining osmotic pressure.

Constituent

Description and Importance

Water

90% of plasma volume; dissolving and suspending medium for solutes of blood; absorbs heat

Electrolytes

Most abundant solutes by number; help maintain plasma osmotic pressure and normal blood pH

Plasma proteins

Albumin (60%): carrier, buffer, osmotic pressure; Globulins (36%): transport and antibodies; Fibrinogen (4%): forms fibrin threads of blood clot

Table: Composition of Plasma (proteins and electrolytes)

Constituent

Description and Importance

Nonprotein nitrogenous substances

By-products of metabolism (urea, uric acid, creatinine, etc.)

Nutrients (organic)

Materials absorbed from digestive tract (glucose, amino acids, fatty acids, etc.)

Respiratory gases

Oxygen (bound to hemoglobin) and carbon dioxide (dissolved or as bicarbonate)

Hormones

Steroid and thyroid hormones carried by plasma proteins

Table: Composition of Plasma (other solutes)

Formed Elements

The formed elements of blood include erythrocytes (red blood cells), leukocytes (white blood cells), and platelets. Only leukocytes are complete cells; erythrocytes lack nuclei and organelles, and platelets are cell fragments. Most formed elements are short-lived and originate in the bone marrow.

Blood cells: erythrocytes, leukocytes, and platelets

Erythrocytes (Red Blood Cells)

Structure and Function

Erythrocytes are small, biconcave, anucleate cells specialized for gas transport. Their shape increases surface area for gas exchange, and they are filled with hemoglobin, the protein responsible for oxygen transport. The absence of mitochondria ensures that erythrocytes do not consume the oxygen they carry.

Structure of erythrocytes (side and top view)

  • Hemoglobin: Each molecule consists of four polypeptide chains (two alpha, two beta) and four heme groups, each containing an iron atom that binds oxygen.

  • Oxygen transport: Each RBC contains about 250 million hemoglobin molecules, each carrying up to four oxygen molecules.

Structure of hemoglobin: globin chains and heme group

Production and Regulation

Red blood cell production (erythropoiesis) occurs in red bone marrow from hematopoietic stem cells. The process is regulated by the hormone erythropoietin (EPO), primarily released by the kidneys in response to hypoxia (low oxygen levels).

Erythropoiesis: formation of red blood cells EPO mechanism for regulating erythropoiesis

  • Dietary requirements: Iron, vitamin B12, folic acid, amino acids, lipids, and carbohydrates are essential for erythropoiesis.

Disorders of Erythrocytes

  • Anemia: Reduced oxygen-carrying capacity due to blood loss, insufficient RBC production, or increased RBC destruction. Symptoms include fatigue, pallor, and shortness of breath.

  • Sickle-cell anemia: Genetic disorder causing abnormal hemoglobin (HbS), leading to crescent-shaped RBCs that rupture easily and block vessels.

Sickle-cell anemia: normal vs. sickled erythrocytes

Leukocytes (White Blood Cells)

Types and Functions

Leukocytes are the only complete cells among the formed elements and are crucial for defense against disease. They are classified as granulocytes (with visible granules) or agranulocytes (without visible granules).

Types and relative percentages of leukocytes in normal blood Leukocytes: neutrophils, eosinophils, basophils, lymphocytes, monocytes

  • Granulocytes: Neutrophils (bacteria slayers, phagocytic), eosinophils (combat parasites, modulate allergies), basophils (release histamine in inflammation).

  • Agranulocytes: Lymphocytes (T cells and B cells, crucial for immunity), monocytes (differentiate into macrophages, phagocytic).

Neutrophils: multilobed nucleus, pale granules Eosinophil: bilobed nucleus, red granules Basophil: bilobed nucleus, purplish-black granules Lymphocyte: large nucleus, thin rim of cytoplasm Monocyte: kidney-shaped nucleus, abundant cytoplasm

Leukocyte Disorders

  • Leukopenia: Abnormally low WBC count, often drug-induced.

  • Leukemias: Cancers involving overproduction of abnormal WBCs, leading to anemia, bleeding, and increased infection risk.

Platelets

Structure and Function

Platelets are cell fragments derived from megakaryocytes. They play a vital role in hemostasis by forming temporary plugs to seal breaks in blood vessels and releasing chemicals necessary for clotting.

Formation of platelets from megakaryocytes

Hemostasis

Steps of Hemostasis

Hemostasis is the process of stopping bleeding and involves three major steps:

  1. Vascular spasm: Vasoconstriction of damaged blood vessel.

  2. Platelet plug formation: Platelets adhere to exposed collagen fibers and release chemicals to recruit more platelets.

  3. Coagulation: Reinforcement of the platelet plug with fibrin threads, forming a stable blood clot.

Events of hemostasis: vascular spasm, platelet plug, coagulation

Coagulation Pathways

Coagulation involves a cascade of clotting factors leading to the conversion of fibrinogen to fibrin. There are two initial pathways (intrinsic and extrinsic) that converge to a common pathway.

  • Intrinsic pathway: Initiated by factors within the blood.

  • Extrinsic pathway: Initiated by external tissue damage.

Intrinsic and extrinsic pathways of blood clotting Intrinsic and extrinsic pathways of blood clotting (detailed)

Fibrin Mesh and Clot Retraction

Thrombin converts soluble fibrinogen into insoluble fibrin, which forms a mesh that traps blood cells and seals the vessel. Clot retraction and fibrinolysis ensure the clot is removed after healing.

Erythrocytes trapped in a fibrin mesh (scanning electron micrograph)

Blood Clotting Factors

Factor Number

Factor Name

Source

Primary Function

I

Fibrinogen

Liver

Converted to fibrin in clot formation

II

Prothrombin

Liver

Converted to thrombin

IV

Calcium ions (Ca2+)

Diet, bones, plasma

Essential for all stages of coagulation

VIII

Antihemophilic factor (AHF)

Liver, lung, capillaries

Intrinsic pathway; deficiency causes hemophilia A

Table: Blood clotting factors (procoagulants)

Blood Groups and Transfusions

ABO and Rh Blood Groups

Blood groups are determined by the presence or absence of specific antigens (agglutinogens) on the surface of RBCs. The ABO system is based on A and B antigens, while the Rh system is based on the D antigen.

Blood Group

RBC Antigens

Plasma Antibodies

Blood That Can Be Received

A

A

Anti-B

A, O

B

B

Anti-A

B, O

AB

A, B

None

A, B, AB, O (universal recipient)

O

None

Anti-A, Anti-B

O (universal donor)

Table: ABO blood groups

Blood Typing

Blood typing involves mixing blood with antibodies against A and B antigens to observe agglutination. Cross-matching ensures compatibility between donor and recipient.

Blood typing of ABO blood types

Summary Table: Formed Elements of Blood

Cell Type

Description

Number per μl

Function

Erythrocyte

Biconcave, anucleate

4–6 million

Transport O2 and CO2

Neutrophil

Multilobed nucleus, pale granules

3000–7000

Phagocytize bacteria

Lymphocyte

Large nucleus, thin rim of cytoplasm

1500–3000

Immunity (T and B cells)

Monocyte

Kidney-shaped nucleus

100–700

Phagocytosis, develop into macrophages

Eosinophil

Bilobed nucleus, red granules

100–400

Kill parasitic worms, modulate allergies

Basophil

Bilobed nucleus, purplish-black granules

20–50

Release histamine, inflammation

Platelets

Cell fragments

150,000–400,000

Seal small tears, clotting

Table: Summary of formed elements of the blood

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