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Chapter 17: Blood – Structure, Function, and Disorders

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Blood: The Internal Transport System

Overview and Learning Goals

Blood is a specialized fluid tissue essential for maintaining homeostasis and transporting substances throughout the body. This chapter explores the composition, functions, formation, and disorders of blood, as well as its role in clinical diagnostics.

Chapter 17 blood learning goals flowchart

Functions of Blood

Distribution, Regulation, and Protection

  • Distribution: Blood transports oxygen, nutrients, metabolic wastes, and hormones.

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

  • Protection: Prevents blood loss (clotting) and infection (immune response).

Composition of Blood

Physical Characteristics and Components

Blood consists of plasma (liquid matrix) and formed elements (cells and cell fragments). The hematocrit measures the percentage of red blood cells (RBCs) in total blood volume.

  • Plasma: ~90% water, contains proteins (albumin, globulins, clotting factors), nutrients, electrolytes, gases, and hormones.

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

Blood sample centrifugation and components

Formed Elements of Blood

Types and Characteristics

Formed elements are the cellular components of blood, each with distinct functions and lifespans.

  • Erythrocytes: Red blood cells, most numerous, responsible for oxygen transport.

  • Leukocytes: White blood cells, involved in immune defense.

  • Platelets: Cell fragments essential for blood clotting.

Blood cell types in blood smear

Erythrocytes (Red Blood Cells)

Structure and Function

Erythrocytes are biconcave, anucleate cells optimized for gas transport. Their shape increases surface area for efficient oxygen exchange.

  • Biconcave Shape: Enhances flexibility and gas exchange.

  • Hemoglobin: Protein responsible for binding and transporting oxygen.

  • Spectrin: Membrane protein providing structural flexibility.

Erythrocyte shape and dimensions

Hemoglobin Structure

Hemoglobin consists of four globin chains (two alpha, two beta) and four heme groups, each containing iron that binds oxygen.

  • Oxyhemoglobin: Hemoglobin bound to oxygen.

  • Deoxyhemoglobin: Hemoglobin after oxygen release.

  • Carbaminohemoglobin: Hemoglobin bound to carbon dioxide.

Hemoglobin structure and heme group

Production and Life Cycle of Blood Cells

Hematopoiesis and Erythropoiesis

Blood cell formation occurs in red bone marrow from stem cells called hemocytoblasts. Erythropoiesis is the process of RBC production, regulated by erythropoietin (EPO).

  • Developmental Pathway: Hemocytoblast → Proerythroblast → Erythroblast → Reticulocyte → Erythrocyte

  • Regulation: EPO released in response to hypoxia stimulates RBC production.

Erythropoiesis developmental pathway Erythropoiesis hormonal regulation

Life Cycle and Fate of Erythrocytes

RBCs have a lifespan of 100–120 days. Old cells are removed by macrophages, and their components are recycled.

  • Hemoglobin Breakdown: Heme is converted to bilirubin, excreted as bile; globin is broken down to amino acids.

Life cycle of red blood cells Fate of hemoglobin and RBC recycling

Erythrocyte Disorders

Anemia and Polycythemia

Anemia is characterized by reduced oxygen-carrying capacity, while polycythemia involves excess RBCs, increasing blood viscosity.

  • Types of Anemia: Hemorrhagic, hemolytic, aplastic, iron-deficiency, pernicious, thalassemia, sickle-cell.

  • Sickle-Cell Anemia: Caused by a single amino acid substitution in hemoglobin, leading to sickle-shaped RBCs.

Normal and sickle-shaped erythrocytes

Leukocytes (White Blood Cells)

Classification and Functions

Leukocytes are nucleated cells involved in immune defense. They are classified as granulocytes or agranulocytes based on the presence of cytoplasmic granules.

  • Granulocytes: Neutrophils, eosinophils, basophils.

  • Agranulocytes: Lymphocytes, monocytes.

Differential WBC count and classification Granulocyte and agranulocyte morphology

Granulocytes

  • Neutrophils: Most abundant, phagocytize bacteria.

  • Eosinophils: Combat parasitic infections, modulate allergic responses.

  • Basophils: Release histamine and heparin, involved in inflammation.

Neutrophil summary table Basophil summary table

Agranulocytes

  • Lymphocytes: Mount immune responses via direct cell attack or antibody production.

  • Monocytes: Develop into macrophages, phagocytize pathogens.

Lymphocyte summary table Monocyte summary table

Leukopoiesis: Formation of Leukocytes

Stem Cell Differentiation

Leukocytes originate from hemocytoblasts, differentiating into myeloid or lymphoid stem cells, which further develop into specific WBC types.

Stem cell differentiation diagram Leukocyte formation pathway

Platelets (Thrombocytes)

Structure and Function

Platelets are cell fragments derived from megakaryocytes, essential for blood clotting and repair of blood vessels.

  • Developmental Pathway: Hemocytoblast → Megakaryoblast → Promegakaryocyte → Megakaryocyte → Platelets

Platelet summary table Platelet formation pathway

Hemostasis: Prevention of Blood Loss

Phases of Hemostasis

Hemostasis is the process of stopping bleeding, involving vascular spasm, platelet plug formation, and coagulation.

  • Vascular Spasm: Immediate vasoconstriction after vessel injury.

  • Platelet Plug Formation: Platelets adhere to exposed collagen and aggregate.

  • Coagulation: Blood is transformed from liquid to gel, forming a clot.

Endothelial cells and platelet adhesion Hemostasis phases diagram

Coagulation Pathways

Coagulation involves intrinsic and extrinsic pathways, both leading to the formation of prothrombin activator, conversion of prothrombin to thrombin, and transformation of fibrinogen to fibrin.

  • Requirements: Calcium ions, vitamin K, clotting factors.

Coagulation pathway flowchart Coagulation pathway flowchart Coagulation pathway flowchart Blood clot SEM Blood clotting factors table

Blood Disorders

Thromboembolytic and Bleeding Disorders

Blood disorders include excessive clotting (thromboembolytic disorders) and bleeding disorders (thrombocytopenia, hemophilia).

  • Thrombocytopenia: Low platelet count, leading to spontaneous bleeding.

  • Hemophilia: Hereditary deficiency of clotting factors, resulting in prolonged bleeding.

Petechiae in thrombocytopenia Coagulation pathway flowchart

Human Blood Groups

ABO and Rh Blood Groups

Blood groups are determined by antigens (agglutinogens) on RBC membranes. The ABO and Rh systems are clinically significant for transfusions.

  • ABO System: Based on presence of A and/or B antigens; plasma contains anti-A and/or anti-B antibodies.

  • Rh System: Presence of Rh antigen (D) determines Rh+ or Rh– status.

ABO blood group table

Transfusion Reactions and Hemolytic Disease of the Newborn

Transfusion reactions occur when mismatched blood is infused, leading to agglutination and hemolysis. Hemolytic disease of the newborn results from Rh incompatibility between mother and fetus.

Clinical Applications

Plasma Volume Expanders and Diagnostic Blood Tests

Plasma expanders are used to restore blood volume in emergencies. Laboratory blood tests provide valuable diagnostic information about health status.

Summary Table: Formed Elements of the Blood

Cell Type

Description

Cells/μL

Duration of Development (D) and Life Span (LS)

Function

Erythrocyte

Biconcave, anucleate

4-6 million

D: 7 days, LS: 100-120 days

Transport oxygen and carbon dioxide

Neutrophil

Multilobed nucleus, pale granules

3,000-7,000

D: 14 days, LS: hours to days

Phagocytize bacteria

Eosinophil

Bilobed nucleus, red granules

100-400

D: 14 days, LS: hours to days

Kill parasitic worms, modulate allergies

Basophil

Bilobed nucleus, large purple granules

20-50

D: 1-7 days, LS: hours to days

Release histamine, contain heparin

Lymphocyte

Spherical nucleus, pale blue cytoplasm

1,500-3,000

D: days to weeks, LS: hours to years

Mount immune response

Monocyte

U/kidney-shaped nucleus, pale blue cytoplasm

100-700

D: 2-3 days, LS: months

Phagocytosis, develop into macrophages

Platelet

Cytoplasmic fragments, stain deep purple

150,000-400,000

D: 4-5 days, LS: 5-10 days

Seal tears, blood clotting

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