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Blood: Structure, Function, and Disorders – ANP College Study Guide

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Blood – Physical Characteristics

Overview of Blood Properties

Blood is a specialized connective tissue with unique physical and chemical properties that are essential for its functions in the human body.

  • Volume: Adult males contain 5-6L; adult females contain 4-5L.

  • Temperature: Approximately 100.4°F, slightly higher than normal body temperature.

  • Viscosity: Blood is five times as viscous as water, making it more resistant to flow due to the presence of cells and plasma proteins.

  • pH: Ranges from 7.35 to 7.45, making it slightly alkaline.

  • Color: Varies from scarlet (oxygenated) to deep red (deoxygenated).

Microscopic view of blood tissue

Components of Blood

Whole Blood Composition

Blood consists of plasma and formed elements, each with distinct roles.

  • Plasma: 46-63% of blood volume; contains water (92%), plasma proteins (7%), and other solutes (1%).

  • Formed Elements: 37-54% of blood volume; includes red blood cells (RBCs, 99.9%), white blood cells (WBCs), and platelets (0.1%).

Functions of Blood

Transportation

Blood is the primary medium for transporting substances throughout the body.

  • Gases: Oxygen and carbon dioxide are carried by hemoglobin and dissolved in plasma.

  • Nutrients: Absorbed from the GI tract and distributed to tissues.

  • Hormones: Transported from endocrine glands to target organs.

  • Metabolic Wastes: Carried to kidneys for excretion.

Blood transport functions diagram

Regulation

Blood helps maintain homeostasis by regulating temperature, pH, and electrolyte balance.

  • Heat Distribution: Absorbs heat from muscles and distributes it to other tissues.

  • Acid-Base Balance: Neutralizes acids generated by active tissues.

  • Electrolyte Reservoir: Maintains levels of Na+, Ca2+, and other ions.

  • Volume Regulation: Adjusts in response to body water levels.

Protection

Blood provides defense against pathogens and restricts fluid loss.

  • White Blood Cells: Migrate to tissues to fight infections and remove debris.

  • Antibodies: Attack invading organisms and foreign compounds.

  • Clotting: Enzymes form clots to restrict fluid loss.

SEM image of blood clot

Red Blood Cells (Erythrocytes)

Structure and Function

Red blood cells are the most abundant formed elements and are specialized for oxygen transport.

  • Abundance: 4.5-6.3 million/µL in males; 4.2-5.5 million/µL in females.

  • Shape: Biconcave disc (diameter ≈ 8µm, thickness ≈ 2.5µm) increases surface area for gas exchange and flexibility.

  • Organelles: Lack nucleus and most organelles; are membranous bags of hemoglobin.

  • Hemoglobin: Binds and transports O2 and CO2.

Red blood cell structure and dimensions

Hemoglobin Structure

Hemoglobin is a large protein responsible for oxygen transport.

  • Composition: Four polypeptide chains (2 α, 2 β), each with a heme group containing iron.

  • Oxygen Binding: Each iron ion binds one O2 molecule; thus, each hemoglobin can carry four O2 molecules.

Hemoglobin molecule structure

Red Blood Cell Formation (Erythropoiesis)

Process and Regulation

Erythropoiesis is the process of RBC formation, occurring in the red bone marrow.

  • Stem Cells: All blood cells develop from hemocytoblasts.

  • Pathways: Hemocytoblasts differentiate into myeloid and lymphoid stem cells, which give rise to RBCs, WBCs, and platelets.

  • Regulation: Erythropoietin (EPO), produced by kidneys, stimulates RBC production in response to hypoxia.

Control of erythrocyte production Erythropoiesis regulation diagram

Lifecycle and Fate of RBCs

Destruction and Recycling

RBCs have a lifespan of about 120 days and are subjected to mechanical stress.

  • Senescence: Old or damaged RBCs are engulfed by macrophages.

  • Hemolysis: RBCs rupture, and hemoglobin is broken down.

  • Fate of Components: Globin proteins are metabolized; heme is converted to bilirubin, which is transported to the liver and excreted in bile.

  • Bilirubin: Excess bilirubin causes jaundice; its breakdown products color urine and feces.

Complete Blood Count (CBC) and Hematocrit

Clinical Importance

CBC is a routine test to determine the number and proportion of blood cells.

  • Hematocrit: Percentage of blood occupied by RBCs; average is 46% in males, 42% in females.

  • Clinical Significance: Low hematocrit indicates anemia; high values indicate polycythemia.

Hematocrit measurement and values

Blood Disorders

Polycythemia

Polycythemia is an elevated hematocrit with normal blood volume, often due to increased erythropoietin or bone marrow cancer.

  • Effects: Increases blood viscosity, reducing flow.

  • Treatment: Blood dilution with isotonic saline.

  • Application: Endurance athletes may induce polycythemia to enhance performance.

Erythropoiesis regulation diagram

Anemia

Anemia is a condition of abnormally low oxygen-carrying capacity in the blood.

  • Symptoms: Shortness of breath, fatigue, chills.

  • Types: Hemorrhagic (blood loss), hemolytic (RBC rupture), aplastic (bone marrow destruction), iron-deficiency, pernicious (B12 deficiency), thalassemia, sickle cell.

Sickle cell anemia RBCs

Sickle Cell Anemia

Sickle cell anemia is caused by a mutation in the β chain of hemoglobin, resulting in sickle-shaped RBCs that block blood vessels.

  • Genetic Basis: Single mutation in the globin gene.

  • Clinical Effects: Blockage of small vessels, pain, and organ damage.

Sickle cell anemia RBCs

Erythroblastosis Fetalis

A type of hemolytic anemia affecting newborns when an Rh- mother produces antibodies against an Rh+ fetus.

  • Mechanism: Maternal antibodies attack fetal RBCs, causing anemia and hypoxia.

  • Prevention: Blood transfusions and Rh immunoglobulin therapy.

Rh incompatibility in pregnancy Anti-D antibodies in Rh- mother

White Blood Cells (Leukocytes)

Functions and Types

White blood cells defend the body against pathogens and remove toxins, wastes, and abnormal cells.

  • Abundance: 6000-9000/µL of blood.

  • Location: Most are in connective tissues and lymphatic organs.

  • Classification: Granulocytes (neutrophils, eosinophils, basophils) and agranulocytes (lymphocytes, monocytes).

White blood cells in circulation Blood smear showing basophils

Granulocytes

  • Neutrophils: 50-70% of WBCs; first responders to infection; attack bacteria. Neutrophil blood smear

  • Eosinophils: 2-4% of WBCs; defend against parasites and participate in allergic reactions. Eosinophil blood smear

  • Basophils: <1% of WBCs; release histamine and heparin at injury sites. Basophil blood smear

Agranulocytes

  • Monocytes: 2-8% of WBCs; become macrophages in tissues and are aggressive phagocytes.

  • Lymphocytes: 20-30% of WBCs; include T cells (cellular immunity), B cells (antibody production), and NK cells (immune surveillance). Lymphocyte blood smear

Platelets and Hemostasis

Platelet Function

Platelets are cell fragments involved in blood clotting and tissue repair.

  • Production: Released from megakaryocytes in bone marrow.

  • Lifespan: 9-12 days; removed by splenic phagocytes.

  • Abundance: 350,000/µL of blood.

Hemostasis (Blood Clotting)

Hemostasis prevents blood loss and establishes a framework for tissue repair.

  • Vascular Phase: Endothelial cells contract, release chemicals, and become sticky; vascular spasm reduces blood loss.

  • Platelet Phase: Platelets adhere to exposed surfaces and become activated, forming a platelet plug.

  • Coagulation Phase: Fibrinogen is converted to fibrin, trapping RBCs and platelets to form a clot.

SEM image of blood clot Blood clotting process diagram

Clot Retraction and Manipulation

Clot retraction stabilizes the injury site and facilitates tissue repair. Anticoagulant drugs manipulate hemostasis to prevent unwanted clotting.

  • Clot Retraction: Platelets contract, pulling vessel edges together.

  • Anticoagulants: Heparin, Coumadin, Streptokinase, and Aspirin inhibit various steps in clot formation.

Thrombi, Emboli, and Hemophilia

Thrombi are clots that form in intact vessels; emboli are clots that travel in the bloodstream. Hemophilia is a hereditary bleeding disorder due to deficiency of clotting factors.

  • Thrombus: Can obstruct blood flow and cause tissue damage.

  • Embolus: Can cause blockages in critical vessels, leading to stroke or pulmonary embolism.

  • Hemophilia: Most commonly due to lack of Factor VIII (Hemophilia A); X-linked inheritance.

Hemophilia pedigree chart

Blood Type Compatibility

Blood Types and Transfusion

Blood type compatibility is crucial for safe transfusions.

  • Type O negative: Universal donor.

  • Type AB positive: Universal recipient.

  • Rh factor: Important in pregnancy and transfusion reactions.

Summary Table: Blood Cell Types and Functions

Cell Type

Abundance

Function

Red Blood Cells

99.9% of formed elements

Oxygen and carbon dioxide transport

Neutrophils

50-70% of WBCs

Bacterial defense

Lymphocytes

20-30% of WBCs

Immune response

Monocytes

2-8% of WBCs

Phagocytosis

Eosinophils

2-4% of WBCs

Parasite defense, allergy

Basophils

<1% of WBCs

Histamine and heparin release

Platelets

350,000/µL

Clotting

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