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Blood: Structure, Function, and Clinical Relevance

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Blood: Structure, Function, and Clinical Relevance

Introduction to Blood

Blood is a specialized fluid connective tissue essential for transporting substances throughout the body. It consists of cells suspended in a liquid matrix called plasma, and plays a critical role in homeostasis, immunity, and hemostasis.

Composition of Whole Blood

Main Components

  • Plasma: The liquid matrix, making up 55% of blood volume, containing water, proteins, and dissolved solutes.

  • Formed Elements: Cellular components including red blood cells (RBCs), white blood cells (WBCs), and platelets.

Centrifuged blood showing plasma, buffy coat, and red blood cells

Physical Characteristics of Blood

  • Temperature: 38°C (100.4°F), slightly higher than body temperature.

  • pH: Slightly alkaline (7.35–7.45).

  • Volume: ~7% of body weight (5–6 L in males, 4–5 L in females).

Plasma Composition

  • Water: 92% of plasma volume.

  • Plasma Proteins: 7% (Albumins, Globulins, Fibrinogen).

  • Other Solutes: 1% (electrolytes, nutrients, gases, waste products).

Blood composition: plasma and formed elements

Plasma Proteins

  • Albumins (60%): Maintain osmotic pressure and transport substances.

  • Globulins (35%): Include antibodies (immunoglobulins) and transport proteins.

  • Fibrinogen (4%): Soluble protein involved in blood clotting; converts to fibrin during coagulation.

Plasma proteins: albumins, globulins, fibrinogen

Formed Elements of Blood

Types of Formed Elements

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

  • White Blood Cells (Leukocytes): Immune defense; five main types (neutrophils, eosinophils, basophils, lymphocytes, monocytes).

  • Platelets (Thrombocytes): Cell fragments involved in clotting.

Blood smear showing erythrocytes, leukocytes, and platelets

Relative Abundance

  • RBCs: 99.9% of formed elements

  • WBCs and Platelets: <0.1% each

Red Blood Cells (RBCs)

Structure and Function

RBCs are biconcave discs specialized for efficient gas transport. Their shape increases surface area for gas exchange and allows flexibility to pass through capillaries. They lack nuclei and organelles, relying on anaerobic metabolism, and have a lifespan of ~120 days.

Three-dimensional shape of RBCsSectional view of a mature RBCRBCs stacking in capillaries (rouleaux)

Hemoglobin

  • Structure: Each hemoglobin molecule has four subunits (2 alpha, 2 beta chains), each with a heme group containing iron (Fe) that binds oxygen.

  • Function: Transports O2 (as oxyhemoglobin) and CO2 (as carbaminohemoglobin). Releases O2 in tissues and binds CO2 for transport to the lungs.

  • Normal Hemoglobin Levels: Males: 14–18 g/dL; Females: 12–16 g/dL.

Hemoglobin molecule structure

RBC Production (Erythropoiesis)

  • Occurs in red bone marrow from hematopoietic stem cells (HSCs).

  • Requires amino acids, iron, vitamins B12, B6, and folic acid.

  • Stimulated by erythropoietin (EPO), a hormone released by the kidneys in response to hypoxia.

Hematopoiesis: blood cell lineage

RBC Disorders

  • Anemia: Low RBC count, hematocrit, or hemoglobin; causes fatigue, dizziness, cyanosis.

  • Sickle-cell anemia: Abnormal hemoglobin causes sickle-shaped RBCs.

  • Pernicious anemia: Vitamin B12 deficiency due to lack of intrinsic factor.

  • Iron deficiency anemia: Small, pale RBCs due to insufficient iron.

  • Polycythemia: Excess RBCs, increasing blood viscosity and risk of thrombosis.

  • Carbon monoxide poisoning: CO binds hemoglobin with high affinity, preventing O2 transport.

Cyanosis due to low oxygenBlood smear: normal vs. iron deficiency anemiaRBC morphology in different anemiasPolycythemia: increased RBC densityOxygen vs. CO binding to hemoglobinHyperbaric chamber for CO poisoning treatment

Blood Types and Transfusion Compatibility

ABO and Rh Blood Groups

Blood types are determined by the presence or absence of antigens (A, B, Rh) on RBC membranes. The ABO system classifies blood as A, B, AB, or O, while the Rh system classifies as positive (+) or negative (–).

  • Universal donor: O–

  • Universal recipient: AB+

ABO blood types and antigens

Transfusion Reactions (Cross-reactions)

If incompatible blood is transfused, antibodies in the recipient's plasma react with donor RBC antigens, causing agglutination and hemolysis.

Cross-reaction: agglutination and hemolysis

Blood Typing Tests

Blood samples are mixed with anti-A, anti-B, and anti-D (Rh) sera. Agglutination indicates the presence of the corresponding antigen.

Blood typing card with agglutination resultsAnti-A, Anti-B, Anti-D reagentsBlood typing test procedure

Hemolytic Disease of the Newborn (HDN)

Occurs when an Rh– mother carries an Rh+ fetus. Maternal anti-Rh antibodies can cross the placenta in subsequent pregnancies, destroying fetal RBCs. Prevention involves RhoGAM administration to the mother.

HDN: maternal antibodies attacking fetal RBCs

White Blood Cells (WBCs)

Types and Functions

WBCs (leukocytes) are immune cells with nuclei and organelles. They defend against pathogens, remove toxins, and attack abnormal cells. Normal count: 5,000–10,000/μL.

  • Neutrophils: Phagocytize bacteria; most abundant.

  • Eosinophils: Combat parasites and allergens.

  • Basophils: Release histamine; involved in inflammation.

  • Lymphocytes: Adaptive immunity (B and T cells).

  • Monocytes: Become macrophages in tissues.

Types of white blood cellsBlood smear with labeled WBCs and platelets

WBC Production and Disorders

  • All blood cells originate from hemocytoblasts in bone marrow.

  • Myeloid stem cells produce all WBCs except lymphocytes; lymphoid stem cells produce lymphocytes.

  • Leukopenia: Low WBC count.

  • Leukemia: Excessive proliferation of abnormal WBCs.

Platelets and Hemostasis

Platelets

  • Cell fragments derived from megakaryocytes in bone marrow.

  • Essential for blood clotting; lifespan 9–12 days.

  • Normal count: 150,000–500,000/μL.

Hemostasis (Blood Clotting)

Hemostasis is the process of stopping bleeding, involving three phases:

  1. Vascular Phase: Vasoconstriction and release of endothelins.

  2. Platelet Phase: Platelet adhesion and aggregation to form a plug.

  3. Coagulation Phase: Cascade of reactions converting fibrinogen to fibrin, forming a stable clot. Involves intrinsic, extrinsic, and common pathways.

  • Essential factors: Calcium ions, vitamin K, clotting factors I–XIII.

  • Thrombin catalyzes fibrin formation.

  • Anticoagulants (e.g., heparin, antithrombin) regulate clotting.

  • Fibrinolysis: Plasmin digests fibrin, dissolving the clot.

Platelet and Clotting Disorders

  • Thrombocytopenia: Low platelet count.

  • Thrombocytosis: High platelet count.

  • Thrombosis: Formation of a clot within a vessel (thrombus); if it moves, called an embolus.

  • Hemophilia: Genetic deficiency of clotting factors (e.g., Factor VIII), leading to impaired clotting.

Summary Table: Main Components of Blood

Component

Percentage of Whole Blood

Main Function

Plasma

~55%

Transport of nutrients, hormones, proteins, waste

Red Blood Cells

~45%

Oxygen and carbon dioxide transport

White Blood Cells

<1%

Immune defense

Platelets

<1%

Blood clotting

Key Equations

  • Hematocrit (HCT):

Example Application

  • If a blood sample has a total volume of 5 mL and a plasma volume of 3.4 mL, the hematocrit is: This value is low for a woman (normal: ~42%).

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